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A Rare Cause of Cyanosis Since Birth: Hb M-Iwate

Turkish journal of haematology, 2019-11, Vol.36 (4), p.299-301

2019

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Retrospective Evaluation Of Children After Stem Cell Transplantation: Single Center Experience

Çağdaş tıp dergisi, 2019-12, Vol.9 (4), p.359-364

2019

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Iron-refractory iron deficiency anemia

Turkish journal of haematology, 2015-03, Vol.32 (1), p.1-14

2015

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First Observation of Hemoglobin San Diego, a High Oxygen Affinity Hemoglobin Variant, in Turkey

Turkish journal of haematology, 2017-12, Vol.34 (4), p.372-373

2017

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First Report of an SH2D1A Mutation Associated with X-Linked Lymphoproliferative Disease in Turkey

Turkish journal of haematology, 2018, Vol.35 (3), p.200-202

2018

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Hemolytic Uremic Syndrome in an Infant with Primary Hyperoxaluria Type II: An Unreported Clinical Association

Nephron (2015), 2019-01, Vol.142 (3), p.264-270

2019

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Validity of Erythrocyte Indices in Differentiation between Iron Deficiency Anemia and β-Thalassemia Trait in Children

Journal of pediatric academy, 2024-03, Vol.5 (1), p.7-13

2024

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Validity of Erythrocyte Indices in Differentiation between Iron Deficiency Anemia and β-Thalassemia Trait in Children: Iron Deficiency Anemia and β-Thalassemia Trait

Journal of pediatric academy, 2024-02

2024

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Association between Maternal and Infantile Markers of Cobalamin Status During the First Month Post-Delivery

Indian journal of pediatrics, 2018-07, Vol.85 (7), p.517-522

2018

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MYH9-related Disease Caused by an R1165C Mutation in a Child With Previous Diagnosis of Immune Thrombocytopenic Purpura

Journal of pediatric hematology/oncology, 2021-11, Vol.43 (8), p.e1265-e1266

2021

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Targeted Next Generation Sequencing and Diagnosis of Congenital Hemolytic Anemias: A Three Years Experience Monocentric Study

Frontiers in physiology, 2021-05, Vol.12, p.684569-684569

2021

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Functional and Clinical Impact of Novel Tmprss6 Variants in Iron-Refractory Iron-Deficiency Anemia Patients and Genotype-Phenotype Studies

Human mutation, 2014-11, Vol.35 (11), p.1321-1329

2014

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B12 Vitamini Eksikliğine İkincil Hemoliz Bulguları Olan Yaşamı Tehdit Eden Anemi, Trombositopeni ve Beyin Atrofisi

Çukurova Üniversitesi tip fakültesi dergisi, 2014-12, Vol.39 (4)

2014

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COVID-19-associated multisystem inflammatory syndrome in children: Experiences of three centres in Turkey

Modern rheumatology, 2022-02, Vol.32 (2), p.460-466

2022

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Use of Low Dose Oral Midazolam During Invasive Procedures in Pediatric Hematology Patients

Gazi tıp dergisi, 2015-01, Vol.26 (4)

2015

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Disappearance of cerebral cortical atrophy following replacement therapy with vitamin B12 in an infant

Çukurova Üniversitesi tip fakültesi dergisi, 2016-03, Vol.41 (1), p.152

Keskin, Ebru Yılmaz

2016

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The role of Matriptase-2 during the early postnatal development in humans

Haematologica (Roma), 2016-04, Vol.101 (4), p.e126-e128

2016

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Association of CYP3A5 Expression and Vincristine Neurotoxicity in Pediatric Malignancies in Turkish Population

Journal of pediatric hematology/oncology, 2017-08, Vol.39 (6), p.458-462

2017

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Severe vitamin B 12 deficiency in a 15-year-old boy: presentation with haemolysis and pancytopenia

BMJ case reports, 2015-05, p.bcr2015209718

2015

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Severe vitamin B12 deficiency in a 15-year-old boy: presentation with haemolysis and pancytopenia

BMJ case reports, 2015-05, Vol.2015

2015

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Carbonic anhydrase VA deficiency: a very rare case of hyperammonemic encephalopathy

Journal of Pediatric Endocrinology and Metabolism, 2020-10, Vol.33 (10), p.1349-1352

2020

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A rare cause of neonatal hypocalcemia: malignant infantile osteopetrosis

Turkish Journal of Medical Sciences, 2009-06, Vol.39 (3), p.457-460

2009

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Inherited coagulation disorders in Turkish children: A retrospective, single-center cohort study

Transfusion and apheresis science, 2020-06, Vol.59 (3), p.102728-102728, Article 102728

2020

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Hemofili B Moleküler Analizinde Türkiye Deneyimi: F9 Gen Mutasyon Spektrumu ve Genotip-Fenotip Iliskisi

Türkiye klinikleri. Türkiye klinikeri journal of medical sciences. Tıp bilimleri dergisi, 2020-05, Vol.40 (3), p.334-341

2020

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Association of Maternal Vitamin B12 Status With Infant Findings and Neurodevelopment in Vitamin B12-Deficient Breast-fed Babies

Journal of pediatric hematology/oncology, 2022-01, Vol.44 (1), p.e91-e95

2022

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A Rare Cause of Cyanosis Since Birth: Hb M-Iwate

Retrospective Evaluation Of Children After Stem Cell Transplantation: Single Center Experience

Iron-refractory iron deficiency anemia

First Observation of Hemoglobin San Diego, a High Oxygen Affinity Hemoglobin Variant, in Turkey

First Report of an SH2D1A Mutation Associated with X-Linked Lymphoproliferative Disease in Turkey

Hemolytic Uremic Syndrome in an Infant with Primary Hyperoxaluria Type II: An Unreported Clinical Association

Validity of Erythrocyte Indices in Differentiation between Iron Deficiency Anemia and β-Thalassemia Trait in Children

Validity of Erythrocyte Indices in Differentiation between Iron Deficiency Anemia and β-Thalassemia Trait in Children: Iron Deficiency Anemia and β-Thalassemia Trait

Association between Maternal and Infantile Markers of Cobalamin Status During the First Month Post-Delivery

MYH9-related Disease Caused by an R1165C Mutation in a Child With Previous Diagnosis of Immune Thrombocytopenic Purpura

Targeted Next Generation Sequencing and Diagnosis of Congenital Hemolytic Anemias: A Three Years Experience Monocentric Study

Functional and Clinical Impact of Novel Tmprss6 Variants in Iron-Refractory Iron-Deficiency Anemia Patients and Genotype-Phenotype Studies

B12 Vitamini Eksikliğine İkincil Hemoliz Bulguları Olan Yaşamı Tehdit Eden Anemi, Trombositopeni ve Beyin Atrofisi

COVID-19-associated multisystem inflammatory syndrome in children: Experiences of three centres in Turkey

Use of Low Dose Oral Midazolam During Invasive Procedures in Pediatric Hematology Patients

Disappearance of cerebral cortical atrophy following replacement therapy with vitamin B12 in an infant

The role of Matriptase-2 during the early postnatal development in humans

Association of CYP3A5 Expression and Vincristine Neurotoxicity in Pediatric Malignancies in Turkish Population

Severe vitamin B 12 deficiency in a 15-year-old boy: presentation with haemolysis and pancytopenia

Severe vitamin B12 deficiency in a 15-year-old boy: presentation with haemolysis and pancytopenia

Carbonic anhydrase VA deficiency: a very rare case of hyperammonemic encephalopathy

A rare cause of neonatal hypocalcemia: malignant infantile osteopetrosis

Inherited coagulation disorders in Turkish children: A retrospective, single-center cohort study

Hemofili B Moleküler Analizinde Türkiye Deneyimi: F9 Gen Mutasyon Spektrumu ve Genotip-Fenotip Iliskisi

Association of Maternal Vitamin B12 Status With Infant Findings and Neurodevelopment in Vitamin B12-Deficient Breast-fed Babies

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