Z. Akçören

发表

Visceroatrial situs solitus with atrioventricular alignment discordance double outlet right ventricle and superoinferior ventricles: fetal and neonatal echocardiographic findings.

S. Ozkutlu, G. Tekinalp, H. Elshershari, 2002, Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography.

A homozygous nonsense mutation in δ-sarcoglycan exon 3 in a case of LGMD2F

C. Bönnemann, H. Topaloglu, V. Nigro, 2000, Neuromuscular Disorders.

Fibrous hamartoma of infancy: A case report with typical ultrasonographic findings.

B. Yalçın, C. Akyüz, Z. Akçören, 2016, The Turkish journal of pediatrics.

Distinctive Features of Hepatic Steatosis in Children: Is It Primary or Secondary to Inborn Errors of Metabolism?

H. Demir, İ. Saltik-Temizel, D. Orhan, 2021, Pediatric gastroenterology, hepatology & nutrition.

Analysis of ΔF508 Mutation in Cystic Fibrosis Pathology Specimens

T. Coşkun, G. Kale, M. Çağlar, 1994 .

Comparison of three different primer pairs for the detection of Mycobacterium tuberculosis by polymerase chain reaction in paraffin-embedded tissues.

U. Ozcelik, T. Kocagöz, A. Göçmen, 1998, The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease.

Bilateral Wilms tumors: Treatment results from a single center.

A. Varan, B. Yalçın, S. Ekinci, 2019, The Turkish journal of pediatrics.

Merosin-positive congenital muscular dystrophy with mental retardation and cataracts: A new entity in two families

B. Talim, Z. Akçören, H. Topalŏlu, 1997 .

A cross section of autosomal recessive limb-girdle muscular dystrophies in 38 families

J. Beckmann, H. Topaloglu, G. Kale, 2000, Journal of medical genetics.

Pathological case of the month. Fatal hemorrhagic staphylococcal pneumonia.

G. Seçmeer, L. Olcay, Z. Akçören, 1995, Archives of pediatrics & adolescent medicine.

Noncardiac malformations in congenital heart disease: a retrospective analysis of 305 pediatric autopsies.

G. Kale, M. Çağlar, B. Talim, 2005, The Turkish journal of pediatrics.

Detection of Mycobacterium tuberculosis DNA in tissue samples of children with sarcoidosis.

U. Ozcelik, N. Kiper, G. Kale, 1997, Pediatric pulmonology.

Mediastinal Germ Cell Tumors in Childhood

A. Varan, B. Yalçın, T. Kutluk, 2012, Pediatric hematology and oncology.

Deletions in the survival motor neuron gene in Turkish spinal muscular atrophy patients

D. Yalnızoǧlu, H. Topaloglu, S. Pehlivan, 1996, Journal of Inherited Metabolic Disease.

Disseminated alveolar rhabdomyosarcoma in a child with spinal muscular atrophy.

H. Topaloglu, N. Yariş, T. Kutluk, 2002, Journal of pediatric hematology/oncology.

Clinical and Histopathological Study of Merosin-deficient and Merosin-positive Congenital Muscular Dystrophy

H. Topaloglu, G. Kale, M. Çağlar, 2000, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Placental findings of IUGR and non-IUGR.

G. Kale, Ş. Yiğit, M. Yurdakök, 2014, The Turkish journal of pediatrics.

Congenital lipoid adrenal hyperplasia

G. Tekinalp, Z. Akçören, S. Kınık, 1999, Histopathology.

Primary lacrimal sac non-Hodgkin's lymphoma in a child.

A. Varan, H. Kıratlı, M. Büyükpamukçu, 2005, International journal of pediatric otorhinolaryngology.

Pulmonary involvement in a child with ligneous conjunctivitis and homozygous type I plasminogen deficiency

M. Irkec, N. Kiper, V. Schuster, 2001, Pediatric pulmonology.

Merkel cell carcinoma in a child.

B. Talim, M. Cengiz, H. Toy, 2009, Journal of pediatric hematology/oncology.

Inflammatory pseudotumor causing intestinal obstruction: diagnostic and therapeutic aspects.

A. Ciftci, M. Şenocak, M. Çağlar, 1998, Journal of pediatric surgery.

A comparative histopathologic and immunohistopathologic evaluation of cremaster muscles from boys with various inguinoscrotal pathologies.

H. Topaloglu, N. Büyükpamukçu, Z. Akçören, 2001, European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie.

Determinants of Riboflavin Responsiveness in Multiple Acyl-CoA Dehydrogenase Deficiency.

T. Coşkun, H. Topaloglu, B. Talim, 2019, Pediatric neurology.

Calpain-3 deficiency causes a mild muscular dystrophy in childhood.

J. Beckmann, I. Richard, H. Topaloglu, 1997, Neuropediatrics.

A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey

J. Beckmann, C. de Toma, K. Campbell, 1997, Annals of neurology.

Calpain-3 mutations in Turkey

I. Richard, H. Topaloglu, E. Tan, 2006, European Journal of Pediatrics.

A novel mutation in the DGUOK gene in a Turkish newborn with mitochondrial depletion syndrome.

S. Seneca, L. de Meirleir, T. Coşkun, 2011, The Turkish journal of pediatrics.

Histologic Features of the Liver in Type Ia Glycogen Storage Disease: Comparative Study between Different Age Groups and Consecutive Biopsies

E. Karabulut, G. Kale, M. Çağlar, 2002, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Undifferentiated (embryonal) sarcoma of the liver: an intriguing diagnosis in a child.

D. Orhan, I. Karnak, Z. Akçören, 2009, European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie.

Undifferentiated embryonal sarcoma of the liver in a child complicated by haemorrhage

B. Yalçın, B. Çil, M. Büyükpamukçu, 2008, Pediatric Radiology.

Teratoid Wilms’ Tumor. A Unilateral Case

G. Kale, B. Sevinir, E. Kotilŏglu, 1994, Tumori.

A RARE TYPE OF RENAL CELL CARCINOMA IN A GIRL: Hybrid Renal Cell Carcinoma

B. Yalçın, M. Şenocak, V. Kesik, 2010, Pediatric hematology and oncology.

Covered exstrophy with ectopic intestinal tissue and bifid phallus: one-stage repair of a complex abnormality.

I. Karnak, Z. Akçören, Ş. Güçer, 2011, Journal of pediatric surgery.

Multilocular Endocervical Polyp in a Five-Year-Old Girl

M. Şenocak, N. Büyükpamukçu, Z. Akçören, 1993 .

Focal nodular hyperplasia of the liver and elevated alpha fetoprotein level in an infant with isolated hemihyperplasia.

A. Varan, H. Demir, M. Büyükpamukçu, 2008, Journal of pediatric hematology/oncology.

Griscelli syndrome: report of three cases.

I. Saatci, F. Ersoy, T. Küçükali, 1995, Pediatric pathology & laboratory medicine : journal of the Society for Pediatric Pathology, affiliated with the International Paediatric Pathology Association.

Primary ovarian lymphoma in an infant: Report of a case

A. Ciftci, M. Şenocak, V. Köseoğlu, 2010, Surgery Today.

Late-onset hypertrophic pyloric stenosis: definition of diagnostic criteria and algorithm for the management.

S. Ekinci, A. Ciftci, M. Şenocak, 2010, Journal of pediatric surgery.

Transverse testicular ectopia with persistent müllerian duct syndrome.

I. Karnak, Z. Akçören, F. Tanyel, 1997, Journal of pediatric surgery.

Intestinal involvement and vasculopathy in von Recklinghausen's neurofibromatosis.

D. Yalnızoǧlu, F. Sarikayalar, Z. Akçören, 1997, The Turkish journal of pediatrics.

The association of adrenocortical carcinoma and thyroid cancer in a child with Peutz-Jeghers syndrome.

A. Ciftci, M. Şenocak, N. Resta, 2011, Journal of pediatric surgery.

Granulomatous osteomyelitis of the sternum presenting with a parasternal mass: a possible relation to the bacillus Calmette-Guérin vaccine.

M. Çağlar, I. Karnak, Z. Akçören, 1999, Journal of Pediatric Surgery.

Primary Osteosarcoma of the Rib: A Case Report and Review of the Literature.

A. Varan, C. Akyüz, Z. Akçören, 2017, Journal of pediatric hematology/oncology.

Chest wall hamartoma: an alarming chest lesion with a benign course.

A. Ciftci, M. Şenocak, Z. Akçören, 1998, Journal of pediatric surgery.

Primary Paraspinal and Spinal Epidural Non-Hodgkin Lymphoma in Childhood.

A. Varan, B. Yalçın, T. Kutluk, 2020, Journal of pediatric hematology/oncology.

Pediatric nasopharyngeal carcinoma

A. Varan, M. Büyükpamukçu, Serhan Küpeli, 2009, Pediatric blood & cancer.

Adenoidectomy due to obstructive neonatal adenoid hypertrophy secondary to cytomegalovirus infection in an 8-week-old infant

Z. Akçören, U. Akyol, Suay Ozmen, 2006 .

Non-immune hydrops fetalis: A retrospective analysis of 151 autopsies performed at a single center.

B. Talim, G. Utine, Ş. Yiğit, 2018, The Turkish journal of pediatrics.

A case of Pearson syndrome associated with multiple renal cysts

A. Rötig, A. Bakkaloğlu, A. Gürgey, 1996, Pediatric Nephrology.

Xanthoma disseminatum: A child with respiratory system involvement and bronchiectasis

D. Doğru, A. Göçmen, Z. Akçören, 2005, Pediatric pulmonology.

Inguinal Hernia as a Rare Manifestation of Meconium Peritonitis: Report of a Case

S. Ekinci, M. Şenocak, I. Karnak, 2002, Surgery Today.

Results of intraoperative gamma probe survey and frozen section in surgical treatment of parathyroid adenoma in children.

T. Soyer, S. Ekinci, A. Ciftci, 2016, Journal of pediatric surgery.

Cholesteryl Ester Storage Disease: Case Report During Childhood

F. Gürakan, A. Yüce, H. Özen, 1999, Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society.

Polyarteritis nodosa involving the hepatobiliary system in an eight-year-old girl with a previous diagnosis of familial Mediterranean fever.

Z. Akçören, P. Oğuzkurt, F. Tanyel, 2000, European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie.

A newborn with VLCAD deficiency Clinical, biochemical, and histopathological findings

H. Waterham, R. Wanders, T. Coşkun, 2007, European Journal of Pediatrics.

Primary non-Hodgkin lymphoma of the tongue in a child.

B. Yalçın, N. Yariş, T. Kutluk, 1998, Medical and pediatric oncology.

The prognostic factors in children undergoing pulmonary metastatectomy.

A. Ciftci, M. Şenocak, I. Karnak, 2012, The Turkish journal of pediatrics.

Assessment of left ventricular systolic and diastolic functions in children with merosin-positive congenital muscular dystrophy.

N. Ceviz, H. Topaloglu, G. Kale, 2003, International journal of cardiology.

Paratesticular metastasis from Wilms tumor associated with a hydrocele

B. Yalçın, A. Ciftci, M. Şenocak, 2006, Pediatric blood & cancer.

Leigh syndrome in a 3-year-old boy with unusual brain MR imaging and pathologic findings.

I. Saatci, F. Söylemezoğlu, F. Soylemezoğlu, 2000, AJNR. American journal of neuroradiology.

Ectopic thymic tissue as a rare and confusing entity.

M. Şenocak, I. Karnak, Z. Akçören, 2002, European journal of pediatric surgery : official journal of Austrian Association of Pediatric Surgery ... [et al] = Zeitschrift fur Kinderchirurgie.

Good clinical observation is essential before molecular studies

H. Topaloglu, E. Tan, Z. Akçören, 1995, The Lancet.

Glomerulonephritis with crescents in childhood; etiologies and significance of M2 macrophages.

S. Özen, R. Topaloğlu, B. Gülhan, 2022, The Turkish journal of pediatrics.

Fecal calprotectin concentration is increased in children with celiac disease: relation with histopathological findings.

N. Balamtekin, N. Uslu, G. Baysoy, 2012, The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology.

Sensorineural hearing loss as an extra-intestinal manifestation of ulcerative colitis in an adolescent girl with pyoderma gangrenosum

A. Kara, A. Ataş, G. Kanra, 2002, European Journal of Pediatrics.

Rhabdomyosarcoma of the common bile duct: an unusual cause of obstructive jaundice in a child.

E. Parlak, B. Talim, I. Karnak, 2012, The Turkish journal of pediatrics.

Expression of Adhesion and Extracellular Matrix Molecules in the Developing Human Brain

B. Anlar, P. Atilla, M. Kose, 2002, Journal of child neurology.

Post-mortem detection of FLAD1 mutations in 2 Turkish siblings with hypotonia in early infancy

H. Nygaard, H. Sivri, A. Tokatlı, 2018, Neuromuscular Disorders.

Spinal muscular atrophy with progressive myoclonic epilepsy: report of new cases and review of the literature.

E. Mercuri, F. Muntoni, A. Manzur, 2003, Neuropediatrics.

Laminin-alpha 2 chain (merosin M) is preserved in the Walker-Warburg syndrome.

I. Saatci, H. Topaloglu, Z. Akçören, 1996, Neuropediatrics.

Acute pancreatitis in a patient with glutaric acidemia type II.

T. Coşkun, A. Tokatlı, Z. Akçören, 1997, The Turkish journal of pediatrics.

Castleman disease: an unusual diagnosis of a portal mass in an 8-year-old boy.

I. Karnak, Z. Akçören, I. User, 2011, Journal of pediatric surgery.

Diagnostic difficulties in neuronal intestinal dysplasia and segmental colitis.

M. Şenocak, N. Büyükpamukçu, Z. Akçören, 2000, Journal of pediatric surgery.

Magnetic resonance elastography in evaluation of liver fibrosis in children with chronic liver disease

I. Idilman, M. Karçaaltıncaba, M. Haliloğlu, 2023, Insights into Imaging.

Obstructive jaundice resulting from adenocarcinoma of the ampulla of Vater in an 11-year-old boy.

Z. Akçören, O. Akhan, F. Tanyel, 1997, Journal of pediatric surgery.

Hepatic mucormycosis in a child with fulminant hepatic failure.

G. Kanra, M. Ceyhan, Z. Akçören, 1996, The Turkish journal of pediatrics.

Laminin-α2 Chain (Merosin M) is Preserved in the Walker-Warburg Syndrome

I. Saatci, Z. Akçören, Y. Gürer, 1996 .

Intramural tracheobronchial remnants associated with esophageal atresia: diagnostic aids

Z. Akçören, F. Tanyel, A. Hiçsönmez, 1993, Pediatric Surgery International.

Pulmonary involvement in a child with ligneous conjunctivitis and homozygous type I plasminogen deficiency

M. Irkec, N. Kiper, V. Schuster, 2001, Pediatric pulmonology.

Al‐Gazali Skeletal Dysplasia Constitutes the Lethal End of ADAMTSL2‐Related Disorders

R. Stevenson, F. McKenzie, A. Nordgren, 2023, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

mtDNA nt3243 mutation, external ophthalmoplegia, and hypogonadism in an adolescent girl.

V. Seyrantepe, Z. Akçören, M. Ozgüç, 1998, Pediatric neurology.

T-cell lymphoma in a child with multicentric Castleman disease.

G. Kale, M. Büyükpamukçu, C. Akyüz, 2000, Medical and pediatric oncology.