D. Aslan

发表

Critically Evaluating Typologies of Internet Sex Offenders: A Psychological Perspective

D. Aslan, 2011 .

The diagnosis of Trichomonas vaginalis in liquid‐based Pap tests: Correlation with PCR

S. Pambuccian, S. Setty, E. Stelow, 2005, Diagnostic cytopathology.

Limbal stem cell deficiency in patients with inherited stem cell disorder of dyskeratosis congenita

T. Vulliamy, I. Dokal, D. Aslan, 2012, International Ophthalmology.

Dyskeratosis congenita and limbal stem cell deficiency.

D. Aslan, R. F. Akata, 2010, Experimental eye research.

Ewing Sarcoma and Primitive Neuroectodermal Tumor of the Esophagus: Report of a Case and Review of Literature

Andrew D. Johnson, S. Pambuccian, R. S. Andrade, 2010, International journal of surgical pathology.

Pulmonary complications after bone marrow transplantation: an autopsy study from a large transplantation center.

S. Pambuccian, A. Rose, J. Jessurun, 2009, Archives of pathology & laboratory medicine.

Papillary thyroid carcinoma with atypical histiocytoid cells on fine‐needle aspiration

A. Saqi, J. Crapanzano, M. Vazquez, 2009, Diagnostic cytopathology.

Specific mosaic KRAS mutations affecting codon 146 cause oculoectodermal syndrome and encephalocraniocutaneous lipomatosis

M. Ahmadian, E. Percin, B. Wollnik, 2016, Clinical genetics.

Peripheral Blood Erythrocyte Parameters in Β-Thalassemia Minor with Coexistent Iron Deficiency: Comparisons between Iron-Deficient and -Sufficient Carriers

D. Aslan, Şeyda Değermenci, 2022, Thalassemia Reports.

The X chromosome: does it have a role in Bloom syndrome, a genomic instability disorder?

D. Aslan, 2014, The Turkish journal of pediatrics.

Is Hemoglobin D Trait Hematologically Silent: Comparison With Healthy Controls and β-thalassemia Carriers

D. Aslan, 2019, Journal of pediatric hematology/oncology.

Ischemia Modified Albumin Measured by the Albumin Cobalt Binding Test: A Clinical and Analytical Review

F. Apple, D. Aslan, 2004 .

Trauma as a risk factor for thrombosis in children: a report of three cases.

A. Gürgey, D. Aslan, N. Beşbaş, 2003, The Turkish journal of pediatrics.

Novel Mutation p.Asp374Val of SERPINC1 in a Turkish Family with Inherited Antithrombin Deficiency

D. Aslan, 2021, Turkish journal of haematology : official journal of Turkish Society of Haematology.

A New Case of Human Atransferrinemia with a Previously Undescribed Mutation in the Transferrin Gene

E. Beutler, K. Crain, D. Aslan, 2007, Acta Haematologica.

Dyskeratosis congenita with corneal limbal insufficiency

A. Bideci, P. Cinaz, D. Aslan, 2009, Pediatric blood & cancer.

Leukopenia in Familial Mediterranean Fever: Case Series and Literature Review with Special Emphasis on Pathogenesis

D. Aslan, 2014, Pediatric hematology and oncology.

Homozygous OB-fold variants in telomere protein TPP1 are associated with dyskeratosis congenita-like phenotypes.

J. Fitzgibbon, T. Vulliamy, Nikolas Pontikos, 2018, Blood.

Primary Hemophagocytic Lymphohistiocytosis in Turkish Children

M. Çetin, A. Yüce, A. Gürgey, 2003, Pediatric hematology and oncology.

Accuracy of herpes simplex virus detection in liquid‐based (SurePath) Papanicolaou tests: A comparison with polymerase chain reaction

S. Pambuccian, T. Schacker, K. Savik, 2008, Diagnostic cytopathology.

Use of brain natriuretic peptide to evaluate transfusion‐related acute lung injury

A. Burgher, D. Aslan, N. Laudi, 2004, Transfusion.

An unusual ocular manifestation in Fanconi anemia: Congenital glaucoma

M. Onol, T. Gursel, Z. Kaya, 2005, American journal of hematology.

The search for new approaches to treating type 1 plasminogen deficiency

D. Aslan, R. F. Akata, 2018, Pediatric blood & cancer.

Benefit of high-dose methylprednisolone in comparison with conventional-dose prednisolone during remission induction therapy in childhood acute lymphoblastic leukemia for long-term follow-up

A. Gürgey, M. Tuncer, B. Tunç, 2003, Leukemia.

Children with acute myeloblastic leukemia presenting with extramedullary infiltration: the effects of high-dose steroid treatment.

S. Unal, M. Çetin, S. Ünal, 2004, Leukemia research.

A665G mutation in PRF1 in a Turkish infant with familial hemophagocytic lymphohistiocytosis

D. Aslan, 2011, Pediatric blood & cancer.

Incidence of High Erythrocyte Count in Infants and Young Children With Iron Deficiency Anemia: Re-evaluation of an Old Parameter

D. Aslan, Ç. Altay, 2003, Journal of pediatric hematology/oncology.

DYSPLASIA AND DISORDER OF CELL MEMBRANE ENTIRETY IN IRON-DEFICIENCY ANEMIA

D. Çetinkaya, S. Unal, L. Olcay, 2008, Pediatric hematology and oncology.

Oculoectodermal syndrome: Report of a new case with a broad clinical spectrum

R. Happle, J. Schröder, U. Moog, 2014, American journal of medical genetics. Part A.

Cytologic diagnosis of metastatic seminoma to the prostate and urinary bladder: A case report

S. Pambuccian, J. Jessurun, D. Aslan, 2008, Diagnostic cytopathology.

THE USEFULNESS OF GLYCOSYLATED HEMOGLOBIN (HbA1C) IN DISCRIMINATING BETWEEN IRON DEFICIENCY AND THALASSEMIA

T. Gursel, D. Aslan, 2006, Pediatric hematology and oncology.

Prevalence of Beta Thalassemia Trait in Denizli.

Z. Bolaman, Y. Enli, D. Aslan, 2001, Turkish journal of haematology : official journal of Turkish Society of Haematology.

The effects of high dose methylprednisolone on apoptosis in children with acute lymphoblastic leukemia.

D. Uçkan, M. Tuncer, S. Yetgin, 2003, Clinical and laboratory haematology.

Parvovirus B19 Infection Associated with Severe Aplastic Anemia in an Immunocompetent Patient

D. Uçkan, S. Yetgin, M. Çetin, 2004, Pediatric hematology and oncology.

The Role of Short Course of High-Dose Methylprednisolone in Children with Acute Myeloblastic Leukemia (FAB M2) Presented with Myeloid Tumor

M. Çetin, D. Aslan, G. Hiçsönmez, 2003, Pediatric hematology and oncology.

The diagnosis of trichomonas vaginalis in liquid‐based Pap tests: Morphological characteristics

S. Pambuccian, E. Stelow, D. Aslan, 2005, Diagnostic cytopathology.

Letter to the editor: The mode of inheritance' in differentiation of Fanconi anemia from Dyskeratosis congenita.

D. Aslan, 2008 .

Maternal serum alpha‐fetoprotein levels are normal in Fanconi anemia: Can it be a lack of postnatal inhibition of AFP gene resulting in the elevation?

D. Aslan, R. O. Karabacak, Oner Deniz Aslan, 2017, Pediatric blood & cancer.

Serum α‐fetoprotein level in Fanconi's anemia: Evaluation of 33 Turkish patients

M. Alikaşifoğlu, D. Aslan, Ç. Altay, 2002 .

GRISCELLI SYNDROME: Description of a Case with Rab27A Mutation

D. Aslan, B. Dalgıç, S. Sarı, 2006, Pediatric hematology and oncology.

Metamizole Sodium-Induced Severe Aplastic Anemia and its Recovery with a Short-Course Steroid Therapy

S. Yetgin, M. Çetin, D. Aslan, 2004, Pediatric hematology and oncology.

Fresh Frozen Plasma Plus Iron Therapy in Congenital Hypotransferrinemia in the Second Decade: A Dynamic Approach to Maintaining Hematological Stability

D. Aslan, 2021, Turkish journal of haematology : official journal of Turkish Society of Haematology.

Addition of oral iron to plasma transfusion in human congenital hypotransferrinemia: A 10‐year observational follow‐up with the effects on hematological parameters and growth

D. Aslan, 2018, Pediatric blood & cancer.

Endoscopic ultrasound‐guided fine needle aspiration features of a pancreatic neoplasm with predominantly intraductal growth and prominent tubular cytomorphology: Intraductal tubular carcinoma of the pancreas?

S. Pambuccian, J. Jessurun, V. Adsay, 2008, Diagnostic cytopathology.

Prostatic glands and urothelial epithelium in a seminal vesicle cyst: report of a case and review of pathologic features and prostatic ectopy.

S. Pambuccian, J. Manivel, D. Aslan, 2006, Archives of pathology & laboratory medicine.

Eye Disorders Caused by Limbal Stem Cell Deficiency

D. Aslan, R. F. Akata, 2012 .

Early‐onset autoimmune hemolytic anemia after cladribine therapy for Waldenström's macroglobulinemia

B. Peterson, T. Eastlund, D. Aslan, 2006, Transfusion.

Ki-67 immunoreactivity in the differential diagnosis of pulmonary neuroendocrine neoplasms in specimens with extensive crush artifact.

S. Pambuccian, J. Jessurun, J. Manivel, 2005, American journal of clinical pathology.

Importance of RDW value in differential diagnosis of hypochrome anemias

A. Gürgey, Ç. Altay, F. Gumruk, 2002, American journal of hematology.

Protein modelling to understand FGB mutations leading to congenital hypofibrinogenaemia

L. Alberio, A. Casini, P. de Moerloose, 2017, Haemophilia : the official journal of the World Federation of Hemophilia.

Failure or delay in diagnosing Fanconi anemia--a well-defined genetic disorder.

D. Aslan, 2013, The Turkish journal of pediatrics.

Use of Serum Iron Status and Hemoglobin A2 Levels for Discrimination Between Iron Deficiency and Thalassemia Minor

D. Aslan, 2013, Pediatric hematology and oncology.

Parapharyngeal chordoma: A diagnostic challenge and potential mimic of pleomorphic adenoma on fine‐needle aspiration cytology

S. Pambuccian, J. Manivel, D. Aslan, 2013, Diagnostic cytopathology.

Outcome of Noncatheter-Related Thrombosis in Children: Influence of Underlying or Coexisting Factors

A. Gurgey, D. Aslan, D. Aslan, 2001, Journal of pediatric hematology/oncology.

Parvovirus B19 infection presenting as pre-B-cell acute lymphoblastic leukemia: a transient and progressive course in two children.

B. Anlar, D. Uçkan, E. Ozyurek, 2004, Journal of pediatric hematology/oncology.

Familial Mediterranean fever with a single MEFV mutation: can a deletion resulting in α-thalassemia be the cause?

D. Aslan, 2011, Journal of Human Genetics.

NADH-cytochrome b5 reductase in a Turkish family with recessive congenital methaemoglobinaemia type I

M. Percy, D. Aslan, 2008, Journal of Clinical Pathology.

VIRUS-ASSOCIATED IMMUNE THROMBOCYTOPENIC PURPURA IN CHILDHOOD

S. Yetgin, D. Aslan, İ. Yenicesu, 2002, Pediatric hematology and oncology.

TEMPORARY DYSPLASTIC HEMATOLOGICAL FEATURES DUE TO IRON DEFICIENCY IN A CASE OF POLAND SYNDROME

S. Balcı, D. Aslan, 2004, Pediatric hematology and oncology.

Recessive congenital methemoglobinemia in immediate generations.

M. Percy, D. Aslan, Gülsan Türköz-Sucak, 2016, The Turkish journal of pediatrics.

A CASE OF TOXIC METHEMOGLOBINEMIA FOLLOWING LIDOCAINE APPLICATION FOR CIRCUMCISION

D. Aslan, S. Kirkiz, 2009 .

Fanconi anemia (FA) and squamous cell carcinoma in childhood.

D. Aslan, 2006, International journal of pediatric otorhinolaryngology.

Harris Platelet Syndrome in Patients of Non-Indian Origin

D. Aslan, 2016, Journal of pediatric hematology/oncology.

The Bethesda System 2001 recommendation for reporting of benign appearing endometrial cells in Pap tests of women age 40 years and older leads to unwarranted surveillance when followed without clinical qualifiers.

E. Pirog, J. Crapanzano, M. Harshan, 2007, Gynecologic oncology.

Detection of blaOXA-48 and clonal relationship in carbapenem resistant K. pneumoniae isolates at a tertiary care center in Western Turkey.

B. Otlu, D. Aslan, G. Ece, 2018, Journal of infection and public health.

It is all in the bag: collodion bag versus HistoGel cell block method.

D. Aslan, B. Berg, Heather Wilgenbusch, 2019, Journal of the American Society of Cytopathology.

The psychological aspects of coping with being accused of sexual offences

D. Aslan, 2008 .

Entering the world of sex offenders: an exploration of offending behaviour patterns of those with both internet and contact sex offences against children

Marcia Worrell, R. Edelmann, D. Bray, 2014 .

Elevated serum ferritin level with cataract of spectacular morphology: Hyperferritinemia-cataract syndrome

D. Aslan, R. F. Akata, H. T. Atalay, 2019, Pediatric Hematology & Oncology.

Radiation-induced pathologic complete response of gross nodal disease in recurrent head and neck melanoma

D. Aslan, Z. Lopater, Elizabeth C. Ester, 2015, Applied Radiation Oncology.

Fanconi Anemia: A Rarely Considered Cause of Macrocytosis During Childhood.

D. Aslan, 2017, Journal of pediatric hematology/oncology.

Survival outcomes of liver metastasectomy in colorectal cancer cases: a single-center analysis in Turkey.

İ. Astarcıoğlu, S. Çokmert, I. Oztop, 2014, Asian Pacific journal of cancer prevention : APJCP.

Y. Alanay, M. Çamurdan, D. Aslan, 2023, American journal of medical genetics. Part C, Seminars in medical genetics.

Early-onset drusen in a girl with bloom syndrome: probable clinical importance of an ocular manifestation.

A. Bideci, Z. Kaya, T. Gürsel, 2004, Journal of pediatric hematology/oncology.

c‐kit expression in adenoid cystic carcinoma does not have an impact on local or distant tumor recurrence

P. Gaffney, S. Pambuccian, K. Savik, 2005, Head & neck.

Homozygous OB-fold variants in telomere protein TPP1 are associated with dyskeratosis congenita-like phenotypes.

J. Fitzgibbon, T. Vulliamy, Nikolas Pontikos, 2018, Blood.

Demographic and offence characteristics: a comparison of sex offenders convicted of possessing indecent images of children, committing contact sex offences or both offences

R. Edelmann, D. Aslan, 2014 .