N. Akar

发表

Spatially Explicit Models to Investigate Geographic Patterns in the Distribution of Forensic STRs: Application to the North-Eastern Mediterranean

A. Novelletto, F. Messina, Andrea Finocchio, 2016, PloS one.

Evidence for single origins of 35delG and delE120 mutations in the GJB2 gene in Anatolia

M. Tekin, N. Akar, S. Elsayed, 2004, Clinical genetics.

Neural Tube Defects in Algeria

N. Akar, B. Houcher, S. Begag, 2012 .

High incidence of neural tube defects in Bursa, Turkey.

N. Akar, A. Çavdar, A. Arcasoy, 1988, Paediatric and perinatal epidemiology.

No association between Glu/Asp polymorphism of NOS3 gene and ischemic stroke.

N. Akar, E. Akar, G. Deda, 1999, Neurology.

No association between Glu/Asp polymorphism of NOS3 gene and ischemic stroke

N. Akar, E. Akar, G. Deda, 1999, Neurology.

Effect of Various Genetic Polymorphisms on the Incidence and Outcome of Severe Sepsis

N. Akar, T. Sipahi, H. Poçan, 2006, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Wilson disease mutations associated with uncommon haplotypes in mediterranean patients

A. Angius, N. Akar, P. Vajro, 1996, Human Genetics.

The detection of quantitative serum p53 protein in lung cancer.

N. Akar, E. Şen, U. Gönüllü, 2005, Tuberkuloz ve toraks.

Catalase-Peroxidase Gene (Kat G) Deletion in Isoniazid Resistant Strains of Mycobacterium Tuberculosis ZONAZD DRENÇLM.TUBERCULOZS SULARINDA KATALAZ PEROKSDAZ GEN (KAT G) DELESYONU

N. Akar, D. Aysev, F. Atalay, 2004 .

Melanocortin-4 Receptor Polymorphisms in Turkish Pediatric Obese Patients

N. Akar, D. Demiralp, M. Berberoğlu, 2011, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Sequence analysis of rpoB mutations in rifampin-resistant clinical Mycobacterium tuberculosis isolates from Turkey.

N. Akar, Z. Karahan, F. Atalay, 2004, Microbial drug resistance.

A novel MEFV gene mutation (A511V) in a Chilean FMF patient

N. Akar, E. Akar, A. Öztürk, 2011 .

Is MEFVGene Arg202Gln (605 G>A) A Disease-Causing Mutation?

N. Akar, M. Eki̇m, A. Öztürk, 2008 .

Serum amyloid A1 and tumor necrosis factor-alpha alleles in Turkish Familial Mediterranean Fever patients with and without amyloidosis

N. Akar, M. Eki̇m, M. Hasipek, 2003, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

A note on mutation analysis in familial Mediterranean fever

M. Tekin, N. Akar, M. Eki̇m, 2003, Pediatric Nephrology.

Is the Ala138Gly alteration of MEFV gene important for amyloidosis?

N. Akar, F. Yalçınkaya, E. Akar, 2001, Human mutation.

Familial Mediterranean fever (FMF)-associated amyloidosis in childhood. Clinical features, course and outcome.

M. Tekin, N. Akar, E. Akar, 2001, Clinical and experimental rheumatology.

Arthritis in children with familial Mediterranean fever

M. Tekin, N. Akar, F. Yalçınkaya, 2002, Rheumatology International.

Familial Mediterranean fever and systemic amyloidosis in untreated Turkish patients.

M. Tekin, N. Akar, E. Akar, 2000, QJM : monthly journal of the Association of Physicians.

Clinical, laboratory and molecular characteristics of children with Familial Mediterranean Fever‐associated vasculitis

M. Tekin, N. Akar, F. Yalçınkaya, 2000, Acta paediatrica.

MEFV mutations in multiplex families with familial Mediterranean fever: is a particular genotype necessary for amyloidosis?

M. Tekin, N. Akar, F. Yalçınkaya, 2000, Clinical genetics.

Genotype-phenotype correlation in a large group of Turkish patients with familial mediterranean fever: evidence for mutation-independent amyloidosis.

M. Tekin, A. Elhan, N. Akar, 2000, Rheumatology.

MEFV mutation analysis in Turkish familial Mediterranean fever patients with amyloidosis.

N. Akar, F. Yalçınkaya, E. Akar, 1999, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

*John G F Cleland, Karl Swedberg, on behalf of The International Ecadotril Multi-centre Dose-ranging Study Investigators

S. Shapiro, N. Akar, X. Bosch, 1998 .

Familial Mediterranean fever--amyloidosis and the Val726Ala mutation.

N. Akar, F. Yalçınkaya, M. Mısırlıoğlu, 1998, The New England journal of medicine.

Evaluation of indirect microparticle activity and parameters of thrombin generation test in healthy infants.

N. Akar, Y. Eğin, F. Orhon, 2014, Thrombosis research.

The strong correlation between serum copper level and the copper/zinc ratio to histopathological changes, clinical stage, and prognosis of Hodgkin's disease.

N. Akar, S. Gözdaşoğlu, 2003, Biological trace element research.

Lipoprotein a levels in pediatric migraine.

N. Akar, S. Teber, G. Deda, 2011, Pediatric neurology.

Prevalence of Factor V 1691 G–A (Leiden) and prothrombin G20210A polymorphisms and the risk of venous thrombosis among cancer patients

N. Akar, R. Çam, A. Ulu, 2007, Journal of Thrombosis and Thrombolysis.

Does FVL have an effect on longevity

N. Akar, Y. Eğin, D. Akın, 2014 .

Deletion polymorphism at the angiotensin-converting enzyme gene in Turkish patients with coronary artery disease.

N. Akar, O. Aras, Ș. Cin, 1998, Scandinavian journal of clinical and laboratory investigation.

The Role of Plasminogen Activator Inhibitor-1 Polymorphism, Factor-V-Leiden, and Prothrombin-20210 Mutations in Pulmonary Thromboembolism

N. Akar, D. Ozel, F. Erkekol, 2009, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Plasminogen activator inhibitor-1 gene 4G/5G polymorphism in cancer patients with and without thrombosis

N. Akar, A. Ulu, A. Eroğlu, 2006, Journal of Thrombosis and Thrombolysis.

Identification of novel TUBB1 variants in patients with macrothrombocytopenia

A. Waheed, Y. Oymak, N. Akar, 2020, Turkish journal of medical sciences.

Screening the SLC26A4 gene in probands with deafness and goiter (Pendred syndrome) ascertained from a large group of students of the schools for the deaf in Turkey

M. Tekin, N. Akar, E. Çomak, 2003, Clinical genetics.

Protease activated receptor 1 gene −506 I / D polymorphism in cancer patients with and without venous thrombosis

N. Akar, A. Eroğlu, A. Karabıyık, 2011, European journal of haematology.

The Association of Protease Activated Receptor 1 gene −506 I/D Polymorphism with Disease-Free Survival in Breast Cancer Patients

N. Akar, A. Eroğlu, A. Karabıyık, 2012, Annals of Surgical Oncology.

HOMOZYGOUS 23-bp INSERTION OF ENDOTHELIAL PROTEIN C RECEPTOR GENE IN A CHILD WITH FATAL SEPSIS

N. Akar, A. Kansu, E. Çiftçi, 2007, Pediatric hematology and oncology.

Relationship Between Plasma Leptin, Insulin and Tumor Necrosis Factor Alpha in Obese Children

H. Çaksen, N. Akar, Z. Aycan, 2005, Journal of pediatric endocrinology & metabolism : JPEM.

Frequency of vitamin K oxidoreductase complex subunit-1 (VKORC1) polymorphisms and warfarin dose management in patients with venous thromboembolism

N. Akar, Y. Eğin, N. Demir, 2018, The Pharmacogenomics Journal.

Evaluation of cardiac functions in patients with thalassemia major

N. Akar, N. O. Küçük, T. Sipahi, 1999, Annals of nuclear medicine.

Endothelial Dysfunction and Vitamin D Levels in Kidney Allograft Recipients

S. Sengul, N. Akar, K. Keven, 2012 .

Prevalence of the MEFV gene mutations in childhood polyarteritis nodosa.

A. Bakkaloğlu, S. Özen, S. Ozen, 2007, The Journal of pediatrics.

Reversible Protease-Activated Receptor 1 Downregulation Mediated by Ankaferd Blood Stopper Inducible With Lipopolysaccharides Inside the Human Umbilical Vein Endothelial Cells

E. Yilmaz, N. Akar, I. Haznedaroglu, 2011, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Association between the −402GA, −401GT, and −323ins10-bp polymorphisms of factor VII gene and breast cancer

N. Akar, A. Öztürk, A. Eroğlu, 2011, Breast cancer.

657del5 mutation in the NBS1 gene is associated with Nijmegen breakage syndrome in a Turkish family

M. Tekin, N. Akar, G. Oǧur, 2002, Clinical genetics.

Screening of EPCR gene mutations in children with acute lymphoblastic leukemia

N. Akar, D. Balı, D. Özkan, 2018 .

Oxygen free radical-dependent increased platelet function in beta-thalassemia major patients.

M. Tekin, F. Violi, N. Akar, 1998, Thrombosis research.

Treatment Challenges in Pediatric Stroke Patients

N. Akar, S. Teber, G. Deda, 2010, Stroke research and treatment.

Thrombotic gene polymorphisms and postoperative outcome after coronary artery bypass graft surgery

N. Akar, Y. Alakoç, Y. Eğin, 2011, Journal of cardiothoracic surgery.

The KBG syndrome: Confirmation of autosomal dominant inheritance and further delineation of the phenotype

M. Tekin, N. Akar, M. Eki̇m, 2004, American journal of medical genetics. Part A.

Epstein-Barr virus genotypes in AIDS-associated lymphomas are similar to those in endemic Burkitt's lymphomas.

D. Shibata, K. Bhatia, I. Magrath, 1992, Leukemia.

Burkitt's lymphoma between African and American types in Turkish children: clinical, viral (EBV), and molecular studies.

I. Magrath, N. Akar, A. Çavdar, 1993, Medical and pediatric oncology.

Plasminogen Activator Inhibitor-1 (PAI-1) Gene Polymorphism (-675 4G/SG) Associated with Obesity and Vascular Risk in Children

N. Akar, Z. Şıklar, M. Berberoğlu, 2006, Journal of pediatric endocrinology & metabolism : JPEM.

A germline PTEN mutation with manifestations of prenatal onset and verrucous epidermal nevus

M. Tekin, C. Eng, N. Akar, 2006, American journal of medical genetics. Part A.

9 Neural Tube Defects in Algeria

N. Akar, B. Houcher, S. Begag, 2012 .

Polymorphisms of 5,10-Methylenetetrahydrofolate Reductase and Cystathionine β-Synthase Genes as a Risk Factor for Neural Tube Defects in Sétif, Algeria

E. Yilmaz, N. Akar, B. Houcher, 2010, Pediatric Neurosurgery.

Relationship Between Functional Promoter Polymorphism in the XBP1 Gene (-116C/G) and Obesity

E. Yilmaz, N. Akar, M. Berberoğlu, 2010, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Relationship between functional promoter polymorphism in the XBP1 gene (−116C/G) and atherosclerosis, ischemic stroke and hyperhomocysteinemia

E. Yilmaz, N. Akar, Y. Adiguzel, 2009, Molecular Biology Reports.

Plasminogen Activator Inhibitor-1 4G/5G Polymorphism in Turkish Children With Cerebral Infarct and Effect on Factor V 1691 A Mutation

E. Yilmaz, N. Akar, E. Akar, 2001, Journal of child neurology.

Effect of plasminogen activator inhibitor-1 4G/5G polymorphism in Turkish deep vein thrombotic patients with and without FV1691 G-A.

E. Yilmaz, N. Akar, A. Yalçın, 2000, Thrombosis research.

A novel deletion in a Turkish beta-thalassemia patient detected by DGGE and direct sequencing: FSC 22-24 (-7 bp).

B. Kirdar, H. Ozçelik, N. Akar, 1993, Hemoglobin.

Paternal X could relate to arithmetic function; study of cognitive function and parental origin of X chromosome in Turner syndrome

M. Tekin, N. Akar, Z. Aycan, 2008, Pediatrics international : official journal of the Japan Pediatric Society.

Genetic Analysis of Afibrinogenemia and Hypofibrinogenemia: Novel Mutations in the FGB Gene in the Turkish Population

N. Akar, N. Sarper, D. Özkan, 2020, Acta Haematologica.

Restriction endonuclease analysis as a solution for determining rifampin resistance mutations by automated DNA sequencing in heteroresistant Mycobacterium tuberculosis strains.

N. Akar, Z. Karahan, 2005, Microbial drug resistance.

Frequency of thiopurine S-methyltransferase gene variations in Turkish children with acute leukemia.

N. Akar, D. Akın, Emin Kürekçi, 2018, The Turkish journal of pediatrics.

The genetic basis of asymptomatic codon 8 frame‐shift (HBB:c25_26delAA) β0‐thalassaemia homozygotes

V. Viprakasit, N. Akar, N. Al-Allawi, 2016, British journal of haematology.

Maternal hair zinc concentration in neural tube defects in Turkey

N. Akar, M. Bahçeci, A. Çavdar, 1991, Biological Trace Element Research.

Zinc status in pregnancy and the occurrence of anencephaly in Turkey.

N. Akar, M. Bahçeci, A. Çavdar, 1988, Journal of trace elements and electrolytes in health and disease.

Is Tissue-Plasminogen Activator Gene Polymorphism a Risk Factor for Venous Thromboembolism in Every Population?

N. Akar, F. Erkekol, N. Ekim, 2005, Journal of Thrombosis and Thrombolysis.

Alterations in Serum Growth Hormone (GH)/GH Dependent Ternary Complex Components (IGF-I, IGFBP-3, ALS, IGF-I/IGFBP-3 Molar Ratio) and the Influence of these Alterations on Growth Pattern in Female Rhythmic Gymnasts

N. Akar, P. Adiyaman, G. Öcal,, 2004, Journal of pediatric endocrinology & metabolism : JPEM.

Asymptomatic hemochromatosis case with HFE c.1007−47G>A, c.340+4T>C heterozygous mutations and alpha globin −3.7 kb deletion

N. Akar, B. Kılıç, F. A. Tükün, 2018, Egyptian Journal of Medical Human Genetics.

Serum pro‐hepcidin levels in infants with iron deficiency anaemia

N. Akar, F. Orhon, B. Ulukol, 2007, International Journal of Laboratory Hematology.

TNF-α −308G/A and IL-6 −174 G/C polymorphisms in the Turkish pediatric stroke patients

A. Elhan, N. Akar, Z. Karahan, 2005 .

Risk factors of neural tube defects: A reality of Batna region in Algeria

N. Akar, B. Houcher, R. Bourouba, 2018, Egyptian Journal of Medical Human Genetics.

Investigation of SLC30A4 and SLC39A14 Zinc Transporter Gene’s Mutations in the Pathogenesis of Neural Tube Defects in Setif, Algeria

N. Akar, R. Bourouba, D. Torun, 2018 .

Possible effects of antioxidant status on increased platelet aggregation in childhood iron‐deficiency anemia

M. Tekin, N. Akar, D. Tekin, 2001, Pediatrics international : official journal of the Japan Pediatric Society.

No significant association between the promoter region polymorphisms of factor VII gene and risk of venous thrombosis in cancer patients.

N. Akar, R. Çam, A. Eroğlu, 2010, Experimental oncology.

THE EFFECTS OF ACUTE INFECTION ON HEMATOLOGICAL PARAMETERS

N. Akar, T. Sipahi, B. Tavil, 2004, Pediatric hematology and oncology.

The role of tumor necrosis factor-alpha -308 G/A and transforming growth factor-beta 1 -915 G/C polymorphisms in childhood idiopathic thrombocytopenic purpura.

N. Akar, Z. Uysal, E. Okulu, 2011, Turkish journal of haematology : official journal of Turkish Society of Haematology.

The molecular basis of β-thalassemia in Turkey

B. Kirdar, A. Özer, N. Akar, 1992, Human Genetics.

E148Q of the MEFV gene causes amyloidosis in familial Mediterranean fever patients.

N. Akar, F. Yalçınkaya, E. Akar, 2001, Pediatrics.

Effect of eNOS and ET-1 Polymorphisms in Thromboangiitis Obliterans

E. Yilmaz, N. Akar, Yekbun Adıgüzel, 2010, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Natural immunity to Haemophilus influenzae type B in children of Ankara, Turkey

N. Akar, F. Özyurda, E. Ocaktan, 2004, Pediatrics international : official journal of the Japan Pediatric Society.

Relationship between susceptibility to antimicrobials and virulence factors in paediatric Escherichia coli isolates.

N. Akar, Ali R. Akin, M. Arısoy, 2008, International Journal of Antimicrobial Agents.

Mutations of the 5α-Steroid Reductase Type 2 Gene in Six Turkish Patients from Unrelated Families and a Large Pedigree of an Isolated Turkish Village

N. Akar, C. Sultan, A. Uysal, 2002, Journal of pediatric endocrinology & metabolism : JPEM.

A novel mutation of 5α-steroid reductase 2 deficiency (CD 65 ALA-PRO) with severe virilization defect in a Turkish family and difficulty in gender assignment

N. Akar, Z. Aycan, Kadir Sipahi, 2010, European Journal of Pediatrics.

A Further Case of Homozygous G20210A Prothrombin Gene Mutation Without Thromboembolic Events

N. Akar, Y. Eğin, 1999, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

High plasma levels of factor VIII: An important risk factor for isolated pulmonary embolism

N. Akar, F. Erkekol, A. Ulu, 2006, Respirology.

Factor V Leiden and prothrombin 20210 G-A mutations in controls and in patients with thromboembolic events during pregnancy or the puerperium

N. Akar, G. Kurtay, M. Yılmazer, 2003, Archives of Gynecology and Obstetrics.

FAMILIAL HIGH FACTOR VIII LEVEL IN A CHILD WITH NECROTIZING FASCIITIS COMPLICATING PRIMARY VARICELLA INFECTION

N. Akar, H. Aydın, A. Kurekci, 2005, Pediatric hematology and oncology.

TNF-alpha -308G/A and IL-6 -174 G/C polymorphisms in the Turkish pediatric stroke patients.

A. Elhan, N. Akar, Z. Karahan, 2005, Thrombosis research.

Detection of TET2 , KRAS and CBL variants by Next Generation Sequencing and analysis of their correlation with JAK2 and FLT3 in childhood AML

N. Akar, M. Bahçe, D. Akın, 2016 .

Detection of TET 2 , KRAS and CBL variants by Next Generation Sequencing and analysis of their correlation with JAK 2 and FLT 3 in childhood AML

N. Akar, M. Bahçe, D. Akın, 2016 .

Diffuse Cerebral Infarct Associated With Factor V Leiden and Prothrombin 20210A Mutations in a Patient With Tetralogy of Fallot

N. Akar, S. Karademir, T. Sipahi, 2009, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

The Prevalence of Methylenetetrahydrofolate Reductase 677 C-T, Factor V 1691 G-A, and Prothrombin 20210 G-A Mutations in Healthy Populations in Sétif, Algeria

N. Akar, B. Houcher, Y. Eğin, 2009, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Coexistence of two prothrombotic mutations, factor V 1691 G-A and prothrombin gene 20210 G-A, and the risk of cerebral infarct in pediatric patients.

N. Akar, E. Akar, G. Deda, 1999, Pediatric hematology and oncology.

PCR evaluation of false-positive signals from two automated blood-culture systems.

N. Akar, D. Aysev, N. Balaban, 2006, Journal of medical microbiology.

Genotype distribution of Candida albicans isolates by 25S intron analysis with regard to invasiveness

N. Akar, D. Aysev, H. Güriz, 2004, Mycoses.

SOLUBLE ENDOTHELIAL PROTEIN C RECEPTOR LEVEL IN CHILDREN WITH SEPSIS

N. Akar, E. Çiftçi, T. Kendirli, 2009, Pediatric hematology and oncology.

Lipoprotein (a) Levels in Childhood Arterial Ischemic Stroke

N. Akar, S. Teber, G. Deda, 2010, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

PT G20210A, factors V G1691A and 1299 His-Arg mutations and tamoxifen-associated thromboembolism in patients with breast cancer.

N. Akar, R. Çam, A. Eroğlu, 2003, Thrombosis research.

Factor VIII levels in children with thrombosis

N. Akar, A. Kurekci, Hafize Gokce, 2003, Pediatrics international : official journal of the Japan Pediatric Society.

Cerebral Sinovenous Thrombosis in Children and Neonates

N. Akar, B. Atasay, S. Arsan, 2015, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

The α2 Gene Alleles of the Platelet Collagen Receptor Integrin α2β1 in Turkish Children with Cerebral Infarct

N. Akar, E. Akar, G. Deda, 2001 .

The Effect of FV-426 G/A Gene Variation on the Occurrence of Thrombosis

N. Akar, A. Öztürk, 2014, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Determination of Factor V Leiden Mutation and R2 Polymorphism in Cis Position

N. Akar, A. Öztürk, Sezen Ballı, 2013, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Factor V Leiden and Prothrombin 20210A Mutations among Turkish Pediatric Leukemia Patients

N. Akar, Kadir Sipahi, Y. Eğin, 2012, Leukemia research and treatment.

The frequency of FV G1691A and PT G20210A mutations in an Albanian population.

M. Tekin, N. Akar, Y. Eğin, 2011, Turkish journal of haematology : official journal of Turkish Society of Haematology.

The role of prothrombotic mutations in patients with Buerger's disease.

E. Yilmaz, N. Akar, U. Demirkılıç, 2000, Thrombosis research.

Factor V (His 1299 Arg) in Young Turkish Patients with Cerebral Infarct

E. Yilmaz, N. Akar, E. Akar, 2000, Pathophysiology of Haemostasis and Thrombosis.

Off-pump coronary artery bypass graft surgery after stent implantation in a patient with combined thrombophilic risk factors.

N. Akar, A. Akar, M. Şırlak, 2007, The Canadian journal of cardiology.

Homocysteine levels in Turkish children.

N. Akar, N. Altuntas, E. Suskan, 2004, Turkish journal of haematology : official journal of Turkish Society of Haematology.

FXIII Gene Val34Leu Polymorphism in Turkish Children with Cerebral Infarct

N. Akar, G. Deda, Buket Dönmez, 2007, Journal of child neurology.

Recombinant human growth hormone treatment in children with thalassemia major

N. Akar, S. Akçurin, S. Kemahlı, 1999, Pediatrics international : official journal of the Japan Pediatric Society.

Vascular endothelial growth factor 936 C/T polymorphism in cancer patients.

N. Akar, S. Gulec, R. Çam, 2006, Annals of oncology : official journal of the European Society for Medical Oncology.

Effect of plasminogen activator inhibitor-1 4G/5G polymorphism in Turkish deep vein thromboembolic patients with and without prothrombin 20210 G-A.

E. Yilmaz, N. Akar, E. Akar, 2004, Turkish journal of haematology : official journal of Turkish Society of Haematology.

RECURRENT ARTERIAL THROMBOSIS IN A CHILD: Primary Antiphospholipid Antibody Syndrome

N. Akar, M. Eki̇m, M. Ertem, 2002, Pediatric Hematology & Oncology.

Relation of Soluble Endothelial Protein C Receptor and Cytokines After Allogeneic Hematopoietic Stem Cell Transplantation

N. Akar, M. Ertem, Z. Uysal, 2011, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

The importance of studying inherited hematological disorders in ancient Anatolian populations.

N. Akar, Yeşim Doğan Alakoç, 2011, Turkish journal of haematology : official journal of Turkish Society of Haematology.

The effects of tamoxifen on homocysteine levels in breast cancer patients

N. Akar, Y. Eğin, A. Eroğlu, 2009 .

Factor V Leiden, prothrombin G20210A and methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms and the risk of tamoxifen-associated thromboembolism in breast cancer patients.

N. Akar, A. Eroğlu, 2011, Thrombosis research.

Effects of calcitonin therapy on osteoporosis in patients with thalassemia.

N. Akar, D. Canatan, A. Arcasoy, 1995, Acta haematologica.

The Relation Between Cytokines, Soluble Endothelial Protein C Receptor, and Factor VIII Levels in Turkish Pediatric Stroke Patients

N. Akar, Y. Eğin, G. Deda, 2009, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

A Novel Homozygous Nucleotide Deletion in the JAK2 Gene in a Pediatric Patient with B-cell Precursor Acute Lymphoblastic Leukemia

N. Akar, A. Kürekçi, Çiğdem Arslan, 2012, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Determination of CEBPA mutations in pediatric acute leukemia

N. Akar, Dilara Fatma AkÄ±n BalÄ±, Deniz AÅlar Ãner, 2018 .

Determination of CEBPA mutations by next generation sequencing in pediatric acute leukemia.

N. Akar, D. Akın, D. A. Oner, 2018, Bratislavske lekarske listy.

Novel mutations of integrin αIIb and β3 genes in Turkish children with Glanzmann’s thrombasthenia

N. Akar, H. Tokgoz, U. Çalişkan, 2015, Platelets.

High Factor VIII Antigen Levels are not Associated with Factor VIII Gene Polymorphisms.

N. Akar, T. Duman, H. Gökçe, 2002, Turkish journal of haematology : official journal of Turkish Society of Haematology.

HIGH LEVELS OF FVIII AND FIX IN A PEDIATRIC PATIENT WITH RETINAL ARTERY OCCLUSION

N. Akar, H. Gökçe, 2002, Pediatric hematology and oncology.

Hemoglobin Lansing (Alpha) [HBA2 CD87 (HIS>GLU) (C>A)] in a Turkish Individual Resulting from Another Nucleotide Substitution

N. Akar, A. Öztürk, D. Torun, 2014, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Three risk factors--high lipoprotein (a), elevated FVIII, and FV Leiden--in a pediatric Behçet's disease patient with deep vein thrombosis.

N. Akar, M. Ertem, Z. Uysal, 2002, Thrombosis research.

Association of the tumor necrosis factor-alpha −308 G/A polymorphism with nasal polyposis

N. Akar, M. Gerçeker, Hunkar Batikhan, 2010, European Archives of Oto-Rhino-Laryngology.

Ligneous conjunctivitis, hydrocephalus, hydrocele, and pulmonary involvement in a child with homozygous type I plasminogen deficiency

N. Akar, E. Çiftçi, E. Ince, 2003, European Journal of Pediatrics.

Prothrombin gene 20210 G‐A mutation in the Turkish population

N. Akar, A. Yalçın, F. Avcu, 1998, American journal of hematology.

Frequency of Factor V (1691 G → A) Mutation in Turkish Population

N. Akar, E. Akar, Ș. Cin, 1997, Thrombosis and Haemostasis.

Effects of Ankaferd Hemostat on Helicobacter pylori strains and antibiotic resistance

N. Akar, I. Haznedaroglu, A. Koluman, 2019, Turkish journal of medical sciences.

The relation between soluble endothelial protein C receptor and factor VIII levels and FVIII/sEPCR index in healthy infants.

N. Akar, Y. Eğin, B. Ulukol, 2011, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Soluble endothelial protein C receptor levels in healthy population

N. Akar, Y. Eğin, F. Orhon, 2009, Journal of Thrombosis and Thrombolysis.

Soluble endothelial protein C receptor levels in Behçet patients with and without ocular involvement

N. Akar, F. Yalçındağ, F. Batıoğlu, 2008, Graefe's Archive for Clinical and Experimental Ophthalmology.

EPCR gene A3 haplotype and elevated soluble endothelial protein C receptor (sEPCR) levels in Turkish pediatric stroke patients.

N. Akar, Y. Eğin, G. Deda, 2007, Thrombosis research.

Single Nucleotide Polymorphisms That Affect Homocysteine Levels in Turkish Population

N. Akar, Yasemin Koç, 2009, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Modernizer of Turkey's Pediatrics: Albert Eckstein in Exile

A. Reisman, N. Akar, A. Oral, 2005 .

Ribosomal protein S19 - 631 insertion is an African-originated mutation.

N. Akar, S. Elsayed, E. Elsobky, 2010, Turkish journal of haematology : official journal of Turkish Society of Haematology.

p53 Gene Polymorphisms in the Turkish Population.

N. Akar, E. Akar, Ș. Cin, 1999, Turkish journal of haematology : official journal of Turkish Society of Haematology.

p53 codon 213 (A-G) polymorphism in a Turkish population.

N. Akar, I. Ilhan, S. Erekul, 1995, Pediatric hematology and oncology.

53 Gene Polymorphisms in the Turkish Population

N. Akar, E. Akar, Þükrü Cýn, 2022 .

Screening of FLT 3 Gene Mutations ( FLT 3-ITD and D 835 ) in Turkish Childhood Acute Leukemia Patients

M. Ozturk, N. Akar, A. Kurekci, 2017 .

Cerebral infarct associated with prothrombin gene G 20210 A variant in a Turkish child with cystic fibrosis: an unusual coexistence

N. Akar, E. Çiftçi, T. Sipahi, 1999, European Journal of Haematology.

Novel plasminogen gene mutations in Turkish patients with type I plasminogen deficiency

N. Akar, H. Özdağ, Buket Dönmez-Demir, 2016, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Effect of Factor VIIIc Levels in Pediatric Stroke Patients

N. Akar, G. Deda, Emel Cangöz, 2004, Pediatric hematology and oncology.

Molecular Approach to Turkish Pediatric Stroke Patients.

N. Akar, 2002, Turkish journal of haematology : official journal of Turkish Society of Haematology.

A novel protein C inhibitor gene mutation in pediatric stroke patients after bone marrow transplantation

E. Yilmaz, N. Akar, M. Ertem, 2013, Molecular Biology Reports.

Analysis of Protein C Inhibitor/ SERPINA5

N. Akar, D. Ozkan, Didem Torun Ozkan, 2020 .

Two New Mutations at ERGIC-53 Gene in a Turkish Family

E. Yilmaz, N. Akar, A. Atay, 2011, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Sequencing of the factor 8(F8) coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations, and one rediagnosis of von Willebrand's disease type 2N

J. Oldenburg, O. el-Maarri, N. Akar, 2006, Haemophilia : the official journal of the World Federation of Hemophilia.

Coffee beans pica causing iron and zinc deficiency

N. Akar, F. Söylemez, T. Sipahi, 1997 .

Desferoxamine and Urinary Zinc Excretion in β-Thalassemia Major

N. Akar, S. Kemahlı, Z. Uysal, 1993 .

A degradation-sensitive anionic trypsinogen (PRSS2) variant protects against chronic pancreatitis

N. Malats, F. Real, H. Friess, 2006, Nature Genetics.

Effects of zinc supplementation on linear growth in beta‐thalassemia (A new approach)

N. Akar, A. Çavdar, A. Arcasoy, 1987, American journal of hematology.

Qualitative/Chemical Analyses of Ankaferd Hemostat and Its Antioxidant Content in Synthetic Gastric Fluids

N. Akar, I. Haznedaroglu, A. Koluman, 2016, BioMed research international.

Dual diverse dynamic reversible actions of Ankaferd on EPCR and PAI-1 inside vascular endothelial cells with and without LPS

E. Yilmaz, N. Akar, I. Haznedaroglu, 2011 .

Subtypes of genotype A Candida albicans isolates determined by restriction endonuclease and sequence analyses.

N. Akar, Z. Karahan, 2005, Microbiological research.

Elevated FVIII and FIX level in a Behçet's disease patient with intracardiac thrombosis and pulmonary arterial aneurysms.

N. Akar, F. Atalay, Dilek Ernam, 2005, Thrombosis research.

Disorders of Sexual Development: An Overview of 18 Years Experience in the Pediatric Endocrinology Department of Ankara University

T. Soygür, N. Akar, Z. Şıklar, 2010, Journal of pediatric endocrinology & metabolism : JPEM.

Interferon Treatment of Hepatitis B and C In β-Thalassemia

N. Akar, Z. Uysal, A. Arcasoy, 1995 .

Hemoglobinopathies in the district of Antalya, Turkey.

N. Akar, O. Yeǧin, Ayla Güven, 1993, Pediatric hematology and oncology.

Beta thalassaemia mutations in the Turkish population.

N. Akar, M. Pirastu, A. Cao, 1987, Journal of medical genetics.

Verification of Hb O-Arab [β121(GH4)GLU → LYS] by Dual Restriction Enzyme Analysis

N. Akar, H. Taştan, E. Akar, 1996 .

Haemoglobin O Arab (B121 Glu-Lys) in Turkish Cypriot population.

N. Akar, A. Çavdar, A. Arcasoy, 1984, Journal of medical genetics.

A further case of Hb J-Iran [ beta 77 ( EF 1 ) His Asp ] in Mu ğ la , Turkey

N. Akar, E. Akar, Sibel Özdemir, 2007 .

Blood group genotyping in multi-transfused patients.

N. Akar, Z. Uysal, O. Arslan, 2013, Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis.

Congenital Thrombotic Risk Factors in β-Thalassemia

N. Akar, Y. Eğin, T. Sipahi, 2009, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

The incidence of alpha-thalassemia in Setif, Algeria.

N. Akar, B. Houcher, A. Öztürk, 2010, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Feasibility of restriction enzyme protocols for the molecular diagnosis of abnormal hemoglobins in Turkish population

N. Akar, H. Taştan, E. Akar, 1999, American journal of hematology.

Abnormal hemoglobins in Turkish Cypriots.

N. Akar, A. Çavdar, A. Arcasoy, 1988, Hemoglobin.

Hb Summer Hill or α2β252(D3)Asp→His in a Turkish Family from Cyprus

N. Akar, T. Huisman, A. Çavdar, 1983 .

A multistep process for the dispersal of a Y chromosomal lineage in the Mediterranean area

C. Vernesi, G. Barbujani, A. Novelletto, 2001 .

A multistep process for the dispersal of a Y chromosomal lineage in the Mediterranean area.

C. Vernesi, G. Barbujani, A. Novelletto, 2001, Annals of human genetics.

The Effect of Plasminogen Activator Inhibitor-1 −675 4G/5G Polymorphism on PAI-1 Gene Expression and Adipocyte Differentiation

N. Akar, H. Aktas, Duygu Ozel Demiralp, 2008, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Phylogeographic Refinement and Large Scale Genotyping of Human Y Chromosome Haplogroup E Provide New Insights into the Dispersal of Early Pastoralists in the African Continent

R. Scozzari, P. Moral, F. Cruciani, 2015, Genome biology and evolution.

Phylogeographic analysis of haplogroup E3b (E-M215) y chromosomes reveals multiple migratory events within and out of Africa.

A. Torroni, R. Scozzari, P. Moral, 2004, American journal of human genetics.

Isolated growth hormone (GH) deficiency type IA associated with a 45-kilobase gene deletion within the human GH gene cluster.

N. Akar, P. Mullis, A. Akıncı, 1992, The Journal of clinical endocrinology and metabolism.

A Comparison of Healthy Infants and Adults with Respect to Indirect Microparticle Activity and the Parameters of the Thrombin Generation Test

N. Akar, Y. Eğin, B. Ulukol, 2016, Turkish journal of haematology : official journal of Turkish Society of Haematology.

A novel MYH9 mutation in a beta thalassemia major patient with thrombocytopenia

N. Akar, Didem Torun Ozkan, Didem Torun Ozkan, 2018, Egyptian Journal of Medical Human Genetics.

An Updated Review of Abnormal Hemoglobins in the Turkish Population

N. Akar, 2014, Turkish journal of haematology : official journal of Turkish Society of Haematology.

A review of abnormal hemoglobins in Turkey.

N. Akar, E. Akar, 2007, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Discrimination of Hb D Los Angeles (B121 Glu‐Gln) and Hb Beograd (B121 Glu‐Val) by Dual Restriction Enzyme Analysis

N. Akar, A. Arcasoy, E. Akar, 1995, American journal of hematology.

Hb D-Los Angeles [beta121(GH4)Glu>Gln] and Hb Beograd [beta121(GH4)Glu>Val]: Implications for their laboratory diagnosis and genetic origins.

N. Akar, Aylin Köseler, E. Akar, 2009, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Effect of methylenetetrahydrofolate reductase 677 C-T, 1298 A-C, and 1317 T-C on factor V 1691 mutation in Turkish deep vein thrombosis patients.

N. Akar, A. Yalçın, F. Avcu, 2000, Thrombosis research.

Genome-Wide Transcriptional Reorganization Associated with Senescence-to-Immortality Switch during Human Hepatocellular Carcinogenesis

R. Cetin-Atalay, Biter Bilen, M. Ozturk, 2013, PloS one.

Genetic Profiling of Pediatric Patients with B-Cell Precursor Acute Lymphoblastic Leukemia

N. Akar, Beyza Doğanay Erdoğan, D. F. Akin-Bali, 2022, Journal of Pediatric Genetics.

Tumor necrosis factor alpha-308 gene polymorphism and pseudoexfoliation glaucoma

A. Elhan, N. Akar, Y. Eğin, 2008, Molecular vision.

Spectrum of GJB2 mutations in Turkey comprises both Caucasian and Oriental variants: Roles of parental consanguinity and assortative mating

Mustafa Tekin, M. Tekin, A. İncesulu, 2003, Human mutation.

Effect of zinc supplementation in a Turkish woman with two previous anencephalic infants.

N. Akar, M. Bahçeci, A. Çavdar, 1991, Gynecologic and obstetric investigation.

Serum endothelial monocyte-activating polypeptide-II: a novel biomarker in patients with non-small-cell lung cancer.

N. Akar, F. Ulger, E. Şen, 2008, Clinical lung cancer.

The effects of Ankaferd® Blood Stopper on transcription factors in HUVEC and the erythrocyte protein profile.

E. Yilmaz, N. Akar, I. Haznedaroglu, 2011, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Functional proteomic analysis of Ankaferd® Blood Stopper.

N. Akar, I. Haznedaroglu, Duygu Özel Demiralp, 2010, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Functional proteomic analysis of Ankaferd ®

N. Akar, Lu, D. Demiralp, 2010 .

Antibacterial Activities of Ankaferd Hemostat (ABS) on Shiga Toxin-Producing Escherichia coli and Other Pathogens Significant in Foodborne Diseases

N. Akar, I. Haznedaroglu, A. Koluman, 2017, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Soluble endothelial cell protein C receptor and thrombomodulin levels after renal transplantation

S. Sengul, N. Akar, K. Keven, 2010, International Urology and Nephrology.

Risk of venous thromboembolism associated with single and combined effects of Factor V Leiden, Prothrombin 20210A and Methylenetethraydrofolate reductase C677T: a meta-analysis involving over 11,000 cases and 21,000 controls

A. Folsom, M. den Heijer, M. Cushman, 2013, European Journal of Epidemiology.

Vascular endothelial growth factor gene 936 C/T polymorphism in breast cancer patients

N. Akar, R. Çam, A. Öztürk, 2008, Medical oncology.

Methylenetetrahydrofolate reductase gene polymorphism and risk of premature myocardial infarction

N. Akar, E. Tutar, D. Oral, 2001, Clinical cardiology.

Endothelial Cell Protein C Receptor (EPCR) Gene Exon III, 23 Bp Insertion Mutation in the Turkish Pediatric Thrombotic Patients

N. Akar, E. Akar, D. Özel, 2002, Thrombosis and Haemostasis.

Factor V Leiden and Natural Selection

N. Akar, 2011, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Factor V Leiden in an Urartian, Dating Back to 1000 BC

N. Akar, Y. Alakoç, Y. Eğin, 2010, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Thrombophilia and avascular necrosis of femoral head in kidney allograft recipients.

S. Sengul, N. Akar, K. Keven, 2006, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.

Coexistence of factor V 1691 G–A and factor V 4070 A–G mutation in Turkish thromboembolic patients

E. Yilmaz, N. Akar, E. Akar, 2000, American journal of hematology.

Inherited protein-C deficiency, factor V G 1691 A and FV A 4070 G mutations in a child with internal cerebral venous thrombosis

N. Akar, T. Sipahi, Ç. Üner, 2000, Pediatric Radiology.

Factor V A4070G (His1299Arg) mutation in Turkish pediatric patients with thrombosis.

E. Yilmaz, N. Akar, E. Akar, 2005, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Factor V (his 1299 arg) in Turkish patients with venous thromboembolism

E. Yilmaz, N. Akar, E. Akar, 2000, American journal of hematology.

Homozygosity for the HR2 Haplotype: Is It a Risk Factor for Thrombosis?

E. Yilmaz, N. Akar, E. Akar, 2003, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Factor V Gene (1691A and 4070G) and Prothrombin Gene 20210A Mutations in Patients with Behçet’s Disease

N. Akar, N. Düzgün, A. Ulu, 2003, Pathophysiology of Haemostasis and Thrombosis.

Frequency of FV 1299 His-Arg (A4070G) in Turkish Cypriots.

E. Yilmaz, N. Akar, E. Akar, 2001, Turkish journal of haematology : official journal of Turkish Society of Haematology.

The Importance of Thrombotic Risk Factors in the Development of Idiopathic Sudden Hearing Loss

A. İncesulu, N. Akar, A. Ulu, 2008, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Protein Z G79A polymorphism in Turkish pediatriccerebral infarct patients.

N. Akar, Y. Eğin, G. Deda, 2008, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Intron F G79a polymorphism of the protein Z gene in cancer patients with and without thrombosis

N. Akar, R. Çam, A. Eroğlu, 2009, Journal of Thrombosis and Thrombolysis.

Intron F G79A Polymorphism of the Protein Z Gene in Turkish Behçet Patients

N. Akar, F. Yalçındağ, A. Öztürk, 2012, Current eye research.

Prothrombin Gene 20210 G→A and Factor V Arg 506 to Gln Mutation in a Patient with Buerger's Disease

N. Akar, C. Beyan, A. Yalçın, 2000, Angiology.

Spectrum of anomalies in Fanconi anaemia.

N. Akar, S. Gözdaşoğlu, 1984, Journal of medical genetics.

Identification of four common α-thalassemia gene deletions among a group with hemoglobinopathies in Sétif population, Algeria

N. Akar, B. Houcher, S. Begag, 2013 .

Differential structuring of human populations for homologous X and Y microsatellite loci.

K. Kidd, S. Q. Mehdi, A. Torroni, 1997, American journal of human genetics.

Serum interleukin-2 and interleukin-6 levels in iron deficiency anemia.

N. Akar, Y. Eğin, T. Sipahi, 1998, Pediatric hematology and oncology.

Comprehensive identification of erythrocyte membrane protein deficiency by 2D gel electrophoresis based proteomic analysis in hereditary elliptocytosis and spherocytosis

N. Akar, D. Demiralp, S. Peker, 2012, Proteomics. Clinical applications.

Proteomic identification of erythrocyte membrane protein deficiency in hereditary spherocytosis

N. Akar, D. Demiralp, S. Peker, 2011, Molecular Biology Reports.

C-type lectin domain family 12, member A: A common denominator in Behçet's syndrome and acute gouty arthritis.

N. Akar, A. Gürler, H. Özdağ, 2015, Medical hypotheses.

A case of severe thrombocytopenia due to parvovirus B19 virus.

N. Akar, S. Kemahlı, Z. Uysal, 1996, Pediatric hematology and oncology.

GM‐CSF in the treatment of Fanconi's anaemia

N. Akar, D. Canatan, Z. Uysal, 1994, British journal of haematology.

Pharmacokinetics of recombinant human erythropoietin in children with chronic renal failure

N. Akar, M. Eki̇m, N. Çakar, 2006, International Urology and Nephrology.

Thrombocyte Indices in Pediatric Age Group

N. Akar, Ș. Cin, A. Y. Rad, 2011 .

Evaluation of Erythropoiesis by Serum Transferrin Receptor and Ferritin in Infants Aged 0–6 Months

N. Akar, S. Tezcan, B. Ulukol, 2004, Pediatric hematology and oncology.

Prevalence of Thalassemia and G 6 PD Deficiency in North Cyprus Ș

N. Akar, A. Çavdar, A. Arcasoy, 2008 .

Prevalence of thalassemia and G6PD deficiency in North Cyprus.

N. Akar, A. Çavdar, A. Arcasoy, 1984, Acta haematologica.

A Turkish case of incontinentia pigmenti with a deletion mutation at Inhibitor of kappa B kinase gamma gene

M. Tekin, N. Akar, M. Güneş, 2022, Egyptian Journal of Medical Human Genetics.

Keratin 8 sequence variants in patients with pancreatitis and pancreatic cancer

F. Real, P. Pignatti, P. Moral, 2006, Journal of Molecular Medicine.

Glucose-6-phosphate dehydrogenase gene Ala365Thr mutation in an Iraqi family with confusing clinical differences

N. Akar, S. Ceylaner, Z. Arslan, 2021, Turkish Journal of Biochemistry.

Further delineation of the molecular pathology of Wilson disease in the Mediterranean population

Mario Pirastu, Andrea Angius, A. Cao, 1998, Human mutation.

Familial Mediterranean fever gene (MEFV) mutations in patients with rheumatic heart disease

N. Akar, F. Yalçınkaya, E. Yılmaz, 2002, Heart.

Isolated recurrent pericarditis in a patient with familial Mediterranean fever

N. Akar, T. Kendirli, E. Akar, 2001, European Journal of Pediatrics.

MEFV mutations in Turkish patients suffering from familial Mediterranean fever

N. Akar, F. Yalçınkaya, M. Akçakuş, 2000, Human mutation.

Enlarging the gene-geography of Europe and the Mediterranean area to STR loci of common forensic use: longitudinal and latitudinal frequency gradients

A. Novelletto, F. Messina, Andrea Finocchio, 2018, Annals of human biology.

Behçet's: A Disease or a Syndrome? Answer from an Expression Profiling Study

N. Akar, T. Çandar, H. Özdağ, 2016, PloS one.

'Oxidation stress index' as a possible clinical marker for the evaluation of non-Hodgkin lymphoma

N. Akar, S. Teber, 2011 .

Interferon treatment of hepatitis B and C in beta-thalassemia.

N. Akar, Z. Uysal, A. Arcasoy, 1995, Pediatric hematology and oncology.

A finely resolved phylogeny of Y chromosome Hg J illuminates the processes of Phoenician and Greek colonizations in the Mediterranean

F. Cruciani, A. Novelletto, F. Messina, 2018, Scientific Reports.

Ankaferd Blood Stopper induces apoptosis and regulates PAR1 and EPCR expression in human leukemia cells

N. Akar, D. Akın, Mine Mumcuoğlu, 2015 .

The Role of Platelet-to-Lymphocyte Ratio in the Diagnosis of Infectious Mononucleosis

N. Akar, M. Turan, Yasemin Ardicoglu Akisin, 2017 .

Kikuchi-Fujimoto Disease Associated with Aseptic Meningitis: A Case Report

N. Akar, Ș. Cin, M. Sumer, 2011 .

An Analysis of the Levels of the Soluble Form of the Endothelial Protein C Receptor in Children with Henoch–Schönlein Purpura

N. Akar, M. Eki̇m, F. Yalçınkaya, 2015, Pediatric hematology and oncology.

The molecular basis of beta-thalassemia in Turkey.

H. Ozçelik, N. Akar, A. Tolun, 1992, Human genetics.

The Dual Diverse Dynamic Reversible Effects of Ankaferd Blood Stopper on EPCR and PAI-1 Inside Vascular Endothelial Cells With and Without LPS Challenge

E. Yilmaz, N. Akar, I. Haznedaroglu, 2012, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Mutation analysis in patients of Mediterranean descent with Wilson disease: identification of 19 novel mutations

A. Angius, N. Akar, G. Loudianos, 1999, Journal of medical genetics.

DDAVP Shortens Bleeding Time in Bernard-Soulier Syndrome

N. Akar, S. Kemahlı, D. Canatan, 1994, Thrombosis and Haemostasis.

Syndrome of Congenital Adrenocortical Unresponsiveness to ACTH. Report of Six Patients

N. Akar, Z. Aycan, A. Penhoat, 2001, Journal of pediatric endocrinology & metabolism : JPEM.

ANOREXIA AND ZINC

N. Akar, R. Bakan, 1984, The Lancet.

A note on oseltamivir treatment in a boy with G6PD deficiency.

N. Akar, 2010, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Search for genetic factors favoring thrombosis in Turkish population.

N. Akar, A. Yalçın, F. Avcu, 1998, Thrombosis research.

Incidence of parvovirus B19 infection among thalassemia major patients from Ankara, Turkey.

N. Akar, A. Arcasoy, Y. Eğin, 1995, Pediatric hematology and oncology.

Tuberculous osteomyelitis: an unusual case of tuberculous infection in a child undergoing continuous ambulatory peritoneal dialysis

N. Akar, M. Eki̇m, N. Tümer, 1995, Pediatric Nephrology.

MEFV Mutations in Turkish Patients Suffering from

N. Akar, F. Yalçınkaya, M. Akçakuş, 1999 .

Common mutations at the homocysteine metabolism pathway and pediatric stroke.

N. Akar, D. Ozel, E. Akar, 2001, Thrombosis research.

Interleukin-6 (IL-6) -174 G/C polymorphism in familial Mediterranean fever patients with and without amyloidosis.

N. Akar, Z. Karahan, E. Akar, 2005, Journal of nephrology.

The value of procalcitonin measurements in children with familial Mediterranean fever

N. Akar, M. Eki̇m, F. Yalçınkaya, 2012, Rheumatology International.

Screening of polymorphisms in the folate pathway in Turkish pediatric Acute Lymphoblastic Leukemia patients

N. Akar, Kadir Sipahi, Mine Mumcuoğlu, 2017 .

Ultrastructural changes in the mucosa of the small intestine in patients with geophagia (Prasad's syndrome).

N. Akar, A. Arcasoy, U. Ors, 1990, Journal of pediatric gastroenterology and nutrition.

Diamond-Gardner Syndrome: Autoerythrocyte Sensitization Syndrome

N. Akar, Yasemin Ardıçoğlu Akışın, Z. Karagöz, 2019, Journal of Pediatric Research.

Prevalence of genetic polymorphisms of methylenetetrahydrofolate reductase C677T and angiotensin I-converting enzyme (insertion/deletion) in Sétif population, Algeria

N. Akar, B. Houcher, S. Begag, 2013 .

The role of angiotensin-converting enzyme gene polymorphism in pulmonary thromboembolism

N. Akar, N. Demir, N. Ekim, 2004, Thrombosis and Haemostasis.

MEF2A Sequence Variants in Turkish Population

N. Akar, S. Gulec, Ahmet Ruchan Akar, 2008, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Contribution of clinical, metabolic, and genetic factors on hypertension in obese children and adolescents

N. Akar, Z. Şıklar, M. Berberoğlu, 2011, Journal of pediatric endocrinology & metabolism : JPEM.

No Relation between Angiotensin-Converting Enzyme Gene Polymorphism and Pseudoexfoliation

A. Elhan, N. Akar, O. Tekeli, 2006, Ophthalmic Research.

A truncating mutation in SERPINB6 is associated with autosomal-recessive nonsyndromic sensorineural hearing loss.

M. King, M. Tekin, X. Liu, 2010, American journal of human genetics.

with Autosomal-Recessive Nonsyndromic Sensorineural Hearing Loss

M. Tekin, S. Züchner, X. Liu, 2010 .

Factor V G1691A (Leiden) is a major etiological factor in Egyptian Budd-Chiari syndrome patients.

N. Akar, S. Elsayed, E. Elsobky, 2011, Turkish journal of haematology : official journal of Turkish Society of Haematology.

RED BLOOD CELL INDEXES IN PATIENTS WITH HEREDITARY SPHEROCYTOSIS AND β-THALASSEMIA COMBINATION

N. Akar, H. Gökçe, 2002 .

Homozygous ß-Thalassemia (FCS8-AA) and Hereditary Spherocytosis in the Same Patient.

N. Akar, Z. Uysal, N. Başak, 2001, Turkish journal of haematology : official journal of Turkish Society of Haematology.

alpha-Thalassemia and hereditary spherocytosis in the same patient: the interaction of two diseases.

N. Akar, Z. Uysal, N. Başak, 1998, Pediatric hematology and oncology.

Does early erythropoietin therapy decrease transfusions in anemia of prematurity ?

N. Akar, B. Atasay, S. Arsan, 2002, Indian journal of pediatrics.

Thrombophilic risk factors in epileptic children treated with valproic Acid.

O. Unal, N. Akar, M. Ertem, 2009, Pediatric neurology.

Evaluation of Hypercoagulability in Obese Children With Thrombin Generation Test and Microparticle Release: Effect of Metabolic Parameters

N. Akar, Z. Şıklar, M. Berberoğlu, 2011, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

The prevalence of factor V (G1691A), MTHFR (C677T) and PT (G20210A) gene mutations in arterial thrombosis.

N. Akar, Fusun Ozmen, M. Ozmen, 2009, Ulusal travma ve acil cerrahi dergisi = Turkish journal of trauma & emergency surgery : TJTES.

Factor V Leiden and Prothrombin Gene 20210A Variant in Neonatal Thromboembolism and in Healthy Neonates and Adults: A Study in a Single Center

N. Akar, S. Kemahlı, B. Atasay, 2003, Pediatric hematology and oncology.

A further note on thrombosis in patients with homozygous beta thalassemia

N. Akar, 2006, Thrombosis and Haemostasis.

Chain and Prothrombin by Functional Proteomic Analyses Prohemostatic and Antithrombin Activities of Ankaferd Hemostat Are Linked to Fibrinogen Gamma

N. Akar, I. Haznedaroglu, Y. Eğin, 2014 .

Prohemostatic and Antithrombin Activities of Ankaferd Hemostat Are Linked to Fibrinogen Gamma Chain and Prothrombin by Functional Proteomic Analyses

N. Akar, Naşit Iğci, I. Haznedaroglu, 2012, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

The Role of Factor V Leiden in Adult Patients With Venous Thromboembolism: A Meta-Analysis of Published Studies from Turkey

N. Akar, A. Eroğlu, D. Sertkaya, 2012, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

The incidence of alpha-thalassemia in Iraqi Turks.

N. Akar, A. Öztürk, Arjan Esmael, 2011, Turkish journal of haematology : official journal of Turkish Society of Haematology.

A note on homocysteine levels in children.

N. Akar, G. Deda, Serap Teber Tras, 2009, Thrombosis research.

Pediatric stroke, homocysteine and MTHFR 677C-T and 1298 A-C.

N. Akar, G. Deda, S. Teber, 2006, Journal of pediatric hematology/oncology.

The Effects of Endothelial Protein C Receptor Gene Polymorphisms on the Plasma sEPCR Level in Venous Thrombosis Patients

E. Yilmaz, N. Akar, Y. Eğin, 2011, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Prothrombin gene 20209 C >T along with the first description of a homozygous polymorphism at the 3' downstream region +4 C >T in the Turkish population.

N. Akar, Y. Eğin, H. Ozdag, 2006, Laboratory hematology : official publication of the International Society for Laboratory Hematology.

Methylenetetrahydrofolate reductase gene polymorphism in type 1 diabetes mellitus: Relationship to microvascular complications

N. Akar, Mohammed A AboElAsrar, Y. Eğin, 2012 .

Hemoglobin H Disease in Turkey: Experience from Eight Centers

Y. Oymak, N. Akar, T. Celkan, 2016, Turkish journal of haematology : official journal of Turkish Society of Haematology.

First observation of homozygote Hb Q-Iran (alpha 75 (EF4) Asp-His).

N. Akar, H. Özdağ, I. Yıldız, 2008, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Maternal risk factors in young Egyptian mothers of Down syndrome

N. Akar, S. Elsayed, E. Elsobky, 2009 .

Desferrioxamine and urinary zinc excretion in beta-thalassemia major.

N. Akar, S. Kemahlı, Z. Uysal, 1993, Pediatric hematology and oncology.

Effect of Twice Weekly Versus Daily Iron Treatment in Turkish Children with Iron Deficiency Anemia

N. Akar, T. Sipahi, B. Tavil, 2003, Pediatric hematology and oncology.

Nutritional Factors, Homocysteine and C677T Polymorphism of the Methylenetetrahydrofolate Reductase Gene in Algerian Subjects with Cardiovascular Disease

N. Akar, B. Houcher, S. Begag, 2012 .

Serum superoxide dismutase levels of beta thalassemia patients and effects of high dosage of intravenous desferrioxamine treatment on superoxide dismutase levels.

M. Tekin, N. Akar, Y. Eğin, 1998, Pediatric hematology and oncology.

Zinc levels of serum, plasma, erythrocytes and hair in Turkish women with anencephalic babies.

N. Akar, U. Ertem, A. Çavdar, 1983, Progress in clinical and biological research.

Neural tube defects and Chernobyl?

N. Akar, A. Aytekin, Y. Ata, 1989, Paediatric and perinatal epidemiology.

Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontia.

M. Tekin, N. Akar, H. Özdağ, 2007, American journal of human genetics.

Radioactive fallout and neural tube defects

N. Akar, 2015 .

Combined Genetic Defects in a Child With Ischemic Stroke: Case Report

N. Akar, G. Deda, D. İçağasioğlu, 2002, Journal of child neurology.

Plasminogen activator inhibitor-1 gene 4 G / 5 G polymorphism in patients with breast cancer

N. Akar, R. Çam, A. Ulu, 2006 .

TNF-α-308 G/A Polymorphism in Egyptian Budd-Chiari Syndrome Patients

N. Akar, S. Elsayed, M. Sakr, 2012, Turkish journal of haematology : official journal of Turkish Society of Haematology.

The Effect of Plasminogen Activator Inhibitor-1 -675 4G/5G Polymorphism on Familial Mediterranean Fever (FMF) Disease

N. Akar, M. Eki̇m, Duygu Ozel Demiralp, 2009, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Association of methylenetetrahydrofolate reductase C677T and cystathionine β-synthase polymorphisms in cardiovascular disease in the algerian population.

N. Akar, B. Houcher, S. Begag, 2010, Genetic testing and molecular biomarkers.

Hyperhomocysteinemia and C 677 T Polymorphism of Methylenetetrahydro-folate Reductase Gene in Patients with Cardiovascular Disease

N. Akar, B. Houcher, S. Begag, 2013 .

Platelet Satellitism

N. Akar, Yasemin Ardıçoğlu Akışın, 2019, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Frequency of mtDNA A1555G and A7445G mutations among children with prelingual deafness in Turkey

M. Tekin, A. İncesulu, N. Akar, 2003, European Journal of Pediatrics.

Dihydrofolate reductase (DHRF) 19-bp intron-1 deletion and methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms in breast cancer

N. Akar, Y. Eğin, R. Çam, 2009, Breast Cancer Research and Treatment.

Connexin 26 (GJB2) mutations in the Turkish population: implications for the origin and high frequency of the 35delG mutation in Caucasians

M. Tekin, A. Pandya, S. Blanton, 2001, Human Genetics.

Angiotensin I Converting Enzyme, Angiotensin II Type 1 Receptor and Angiotensinogen Polymorphisms and Early Myocardial Infarction in Turkish Population

N. Akar, C. Ermiş, N. Hanson, 2002, Thrombosis and Haemostasis.

First observation of hemoglobin Crete [Beta129(H7) Ala>Pro] in the Turkish population.

N. Akar, Çiğdem Arslan, S. Kahraman, 2011, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Premarital screening in Muğla Region of Turkey.

N. Akar, Sibel Özdemir, Ismail Hakki Timur, 2009, Turkish journal of haematology : official journal of Turkish Society of Haematology.

First Observation of Hemoglobin Pyrgos [ß83(EF7) Gly→Asp] in Turkish Population.

N. Akar, A. Arcasoy, E. Akar, 2003, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Ancient interactions : east and west in Eurasia

R. Villems, J. Parik, F. Cruciani, 2003 .

ISONIAZID-RESISTANT strains of Mycobacterium tuberculosis.

N. Akar, D. Aysev, F. Atalay, 1953, Lancet.

Serum Pro-Hepcidin Levels and Relationship with Ferritin in Healthy Non-Anaemic Infants

N. Akar, F. Orhon, B. Ulukol, 2007, Acta Haematologica.

Patterns of male‐specific inter‐population divergence in Europe, West Asia and North Africa

R. Villems, J. Parik, A. Torroni, 2000, Annals of human genetics.

Homozygous protein C deficiency with a double variant His 202 to Tyr and Ala 346 to Thr.

N. Akar, S. Kemahlı, M. Aiach, 1998, Blood Coagulation and Fibrinolysis.

Endothelial Protein C Receptor and Pediatric Arterial Stroke

N. Akar, G. Deda, A. Karabıyık, 2013, Turkish journal of haematology : official journal of Turkish Society of Haematology.

The correlation between soluble endothelial protein c receptor (sEPCR) and tumor necrosis factor-alpha (TNF-α) levels in vivo.

N. Akar, Y. Eğin, A. Ulu, 2008, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Fetal alcohol syndrome

N. Akar, Nejat Akar, 1997, Acta paediatrica.

Prothrombotic risk factors in childhood migraine and comparison of acetylsalicyclic acid and propranolol in prophylactic therapy

N. Akar, Z. Uysal, G. Deda, 2007, Journal of Pediatric Neurology.

Frequency of five thrombophilic polymorphisms in the Egyptian population.

M. Tekin, N. Akar, E. Elsobky, 2006, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Factor V1691 G-A, Prothrombin 20210 G-A, and Methylenetetrahydrofolate Reductase 677 C-T Variants in Turkish Children With Cerebral Infarct

N. Akar, E. Akar, G. Deda, 1999, Journal of child neurology.

Thrombophilia‐associated gene mutations in women with pregnancies complicated by fetal neural tube defects

N. Akar, Y. Eğin, C. Beyan, 2008, International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.

Endothelial Protein C Receptor gene Expression in a Female with Homozygous EPCR gene 23-bp Insertion

N. Akar, A. Karabıyık, 2011, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Effect of Factor V Leiden on Thrombosis in Childhood Leukemia

N. Akar, D. Akin, 2013 .

The 19-bp deletion of dihydrofolate reductase (DHFR), methylenetetrahydrofolate reductase (MTHFR) C677T, Factor V Leiden, prothrombin G20210A polymorphisms in cancer patients with and without thrombosis

N. Akar, Y. Eğin, R. Çam, 2008, Annals of Hematology.

High iron content of Ankaferd hemostat as a clue for its hemostatic action of red blood cell origin.

N. Akar, I. Haznedaroglu, N. Erduran, 2015, Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis.

Direct detection of Hb C (B6 Glu‐Lys) by BseRI analysis

N. Akar, H. Taştan, E. Akar, 1996, American journal of hematology.

Spatially Explicit Models to Investigate Geographic Patterns in the Distribution of Forensic STRs

A. Novelletto, F. Messina, Andrea Finocchio, 2016, bioRxiv.

Methylenetetrahydrofolate reductase 677 C‐T and homocysteine levels in Turkish patients with pseudoexfoliation

N. Akar, Filiz Özdemir, O. Tekeli, 2005, Clinical & experimental ophthalmology.

Tumor necrosis factor alpha-308 gene polymorphism and pseudoexfoliation glaucoma.

A. Elhan, N. Akar, Y. Eğin, 2008 .

Tumour Necrosis Factor-Alpha Gene Polymorphism (-308 G-A) in Turkish Pediatric Thrombosis Patients.

N. Akar, M. Hasipek, 2002, Turkish journal of haematology : official journal of Turkish Society of Haematology.

A Novel 13 BP Deletion in the 3′UTR of the β-Globin Gene Causes β-Thalassemia in a Turkish Patient

B. Kirdar, A. Özer, N. Akar, 1993 .

The alpha2 Gene alleles of the platelet collagen receptor integrin alpha2 beta1 in Turkish children with cerebral infarct.

N. Akar, E. Akar, G. Deda, 2001, Thrombosis research.

Spina bifida and common mutations at the homocysteine metabolism pathway

N. Akar, S. Arsan, E. Akar, 2000, Clinical genetics.

Maternal plasma zinc levels after oral zinc tolerance test in pregnancies associated with neural tube defects in Turkey : brief report

N. Akar, D. Uçkan, M. Bahçeci, 1991 .

Role of ZIP14 (SLC39A14) gene histidine rich regions in neural tube defects

E. Yilmaz, N. Akar, E. Akar, 2011 .

Neural tube defects and zinc

N. Akar, 1998, Archives of disease in childhood.

Pregnancy outcome of mothers with defective oral zinc tolerance test

N. Akar, 1997 .

Maternal hair zinc, copper and magnesium concentration in neural tube defects in Turkey

N. Akar, N. Dincer, 1995 .

814 Polymorphism of Surfactan Protein B Genes and the Risk of Respiratory Distress Sendrome and Chronic Lung Disease in Preterm Neonates

M. Tekin, N. Akar, B. Atasay, 2010 .

Y chromosomal haplogroup J as a signature of the post-neolithic colonization of Europe

Guido Barbujani, Nicholas P. Anagnou, Kalliopi I. Pappa, 2004, Human Genetics.

Proteomic identification of erythrocyte membrane protein deficiency in hereditary spherocytosis

N. Akar, D. Demiralp, S. Peker, 2012, Molecular Biology Reports.

Factor V Leiden mutation as a predisposing factor for veno-occlusive disease following BMT

N. Akar, M. Ertem, N. Akar, 2000, Bone Marrow Transplantation.

Endothelial nitric oxide synthase intron 4, 27 bp repeat polymorphism in Turkish patients with deep vein thrombosis and cerebrovascular accidents.

N. Akar, A. Yalçın, F. Avcu, 1999, Thrombosis Research.

A Novel Beta Globin Gene Polymorphism in Turkish Population: IVS-II 706 G>A

N. Akar, S. Ceylaner, H. Dogan, 2015 .

Premarital Genetic Diagnosis Revealed Co-heredity Nature of Beta Globin Gene 25-26 del AA and 3’UTR+101 G-C Variants in Two Beta Thalassemia Heterozygotes

N. Akar, K. Yararbaş, Yasemin Ardıçoğlu, 2017, Turkish journal of haematology : official journal of Turkish Society of Haematology.

23‐bp endothelial protein C receptor (EPCR) gene insertion mutation in cancer patients with and without thrombosis

N. Akar, R. Çam, A. Ulu, 2006, American journal of hematology.

Rapid Diagnosis Of Two β-Thalassemia Mutatlons: Frameshift Codon 5 (-CT) And Codon 6 (-A)

N. Akar, A. Özden, 1994 .

A finely resolved phylogeny of Y chromosome Hg J illuminates the processes of Phoenician and Greek colonizations in the Mediterranean

F. Cruciani, A. Novelletto, F. Messina, 2018, Scientific Reports.

Plasminogen activator inhibitor -1 gene 4G/5G polymorphism in patients with breast cancer.

N. Akar, R. Çam, A. Ulu, 2006, Journal of B.U.ON. : official journal of the Balkan Union of Oncology.

T102C polymorphism of the serotonin (5-HT) 2A receptor gene in Turkish children with cerebral infarct.

N. Akar, G. Deda, S. Teber, 2007, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Methylenetetrahydrofolate reductase C677T polymorphism in breast cancer risk

N. Akar, A. Eroğlu, 2010, Breast Cancer Research and Treatment.

Screening of single nucleotide polymorphism in CD95 (APO-1/FAS) promoter region (G-1377A) in children with acute leukemia

N. Akar, Emin Kürekçi, Didem Özkan, 2018 .

PCR evaluation of false-positive signals from two automated blood-culture systems.

N. Akar, D. Aysev, N. Balaban, 2006, Journal of medical microbiology.

Protein Z G 79 A polymorphism in Turkish pediatric cerebral infarct patients

N. Akar, G. Deda, S. Teber, 2008 .

Infant mortality after Chernobyl

R. Dahlhaus, M. Blettner, A. Czeizel, 1990, The Lancet.

A novel protein C inhibitor gene mutation in pediatric stroke patients after bone marrow transplantation

E. Yilmaz, N. Akar, M. Ertem, 2013, Molecular Biology Reports.

Soluble Transferrin Receptor is not a Reliable Marker of Iron Deficiency in Pediatric CAPD Patients

N. Akar, M. Eki̇m, S. Bakkaloğlu, 2002, Peritoneal dialysis international : journal of the International Society for Peritoneal Dialysis.

A. Folsom, M. den Heijer, M. Cushman, 2013, European Journal of Epidemiology.

Lipoprotein (a) Levels in Childhood Arterial Ischemic Stroke

N. Akar, S. Teber, G. Deda, 2010, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Lipoprotein a levels in pediatric migraine.

N. Akar, S. Teber, G. Deda, 2011, Pediatric neurology.

First observation of homozygous hemoglobin hamadan (B 56 (D7) GLY‐ARG) and beta thalassemia (‐29 G>A)‐ hemoglobin Hamadan combination in a Turkish family

N. Akar, E. Akar, Sibel Özdemir, 2003, American journal of hematology.

Plasma endothelin-1 levels in patients with left-to-right shunt with or without pulmonary hypertension.

N. Akar, S. Atalay, H. Tutar, 1999, International journal of cardiology.

Mutation analysis in patients of Mediterranean descent with Wilson disease: identification of 19 novel mutations

A. Angius, N. Akar, G. Loudianos, 1999, Journal of medical genetics.