Berna Atabay

Tepecik, Turkey

Last Updated: 09/26/2026

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Found 14 publications

Homozygous c.130-131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry.

Homozygous c.130-131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry.

Journal: Pediatric blood & cancer

Published: November 13, 2018

Intracranial Bleeding in a Female Hemophilia Patient: Molecular Analysis of the Factor 8 Gene and Determination of a Novel Mutation

Intracranial Bleeding in a Female Hemophilia Patient: Molecular Analysis of the Factor 8 Gene and Determination of a Novel Mutation

Journal: Turkish journal of haematology : official journal of Turkish Society of Haematology

Published: February 03, 2018

Evaluation of the Clinical and Laboratory Characteristics of Previously Followed-up Thalassemia Intermedia Patients to Provide Them Better Care in the Future.

Evaluation of the Clinical and Laboratory Characteristics of Previously Followed-up Thalassemia Intermedia Patients to Provide Them Better Care in the Future.

Journal: Journal of pediatric hematology/oncology

Published: July 19, 2017

A National Registry of Thalassemia in Turkey: Demographic and Disease Characteristics of Patients, Achievements, and Challenges in Prevention.

A National Registry of Thalassemia in Turkey: Demographic and Disease Characteristics of Patients, Achievements, and Challenges in Prevention.

Journal: Turkish journal of haematology : official journal of Turkish Society of Haematology

Published: April 14, 2017

Pure Red Cell Aplasia Due to Parvovirus B19: Erythropoietin-Resistant Anemia in a Pediatric Kidney Recipient.

Pure Red Cell Aplasia Due to Parvovirus B19: Erythropoietin-Resistant Anemia in a Pediatric Kidney Recipient.

Journal: Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation

Published: April 08, 2017

Juvenile Myelomonocytic Leukemia in Turkey: A Retrospective Analysis of Sixty-five Patients.

Juvenile Myelomonocytic Leukemia in Turkey: A Retrospective Analysis of Sixty-five Patients.

Journal: Turkish journal of haematology : official journal of Turkish Society of Haematology

Published: February 10, 2017

Lack of Early Inflammation Signs of Acute Compartment Syndrome in an Immunodeficient Patient.

Lack of Early Inflammation Signs of Acute Compartment Syndrome in an Immunodeficient Patient.

Journal: Turkish journal of haematology : official journal of Turkish Society of Haematology

Published: April 21, 2016

Difficult diagnosis of invasive fungal infection predominantly involving the lower gastrointestinal tract in acute lymphoblastic leukaemia.

Difficult diagnosis of invasive fungal infection predominantly involving the lower gastrointestinal tract in acute lymphoblastic leukaemia.

Journal: Medical mycology case reports

Published: November 04, 2015

Frequency of red cell allo- and autoimmunization in patients with transfusion-dependent beta thalassemia and affecting factors.

Frequency of red cell allo- and autoimmunization in patients with transfusion-dependent beta thalassemia and affecting factors.

Journal: The Turkish journal of pediatrics

Published: May 30, 2015

The investigation of relationship between joint findings and serum angiogenic and inflammatory factor levels in severe hemophilia A patients.

The investigation of relationship between joint findings and serum angiogenic and inflammatory factor levels in severe hemophilia A patients.

Journal: Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis

Published: May 23, 2014

Heart rate variability in β-thalassaemia major with or without cardiac siderosis.

Heart rate variability in β-thalassaemia major with or without cardiac siderosis.

Journal: Cardiology in the young

Published: February 14, 2013

X-linked agammaglobulinemia presenting with secondary hemophagocytic syndrome: a case report.

X-linked agammaglobulinemia presenting with secondary hemophagocytic syndrome: a case report.

Journal: Case reports in medicine

Published: November 13, 2012

Showing 1-12 of 14

Last Updated: 09/26/2026