Lista de obras -

A 17-year experience with ALL-BFM protocol in acute lymphoblastic leukemia: prognostic predictors and interruptions during protocol.

artículo científico publicado en 2014

A Case with Gaucher-Like Cells

A Case with Micromegakaryocytes

artículo científico publicado en 2001

A Possible Role for WNT5A Hypermethylation in Pediatric Acute Lymphoblastic Leukemia.

artículo científico publicado en 2015

A child presenting with hypercalcemia.

artículo científico publicado en 2014

A new family with hereditary hyperferritinemia cataract syndrome

artículo científico publicado en 2013

A novel combined treatment for plasminogen deficiency with lung involvement

scientific article published on 04 November 2019

A rare cause of thrombocyte dysfunction: Hermansky-Pudlak syndrome

artículo científico publicado en 2014

Accidental High-dose Intrathecal Treatment: Late Results of a Patient

scientific article published on 17 September 2019

Adrenal masses in children: Imaging, surgical treatment and outcome

scientific article published on 06 April 2019

Alcaligenes xylosoxidans bacteremia in a patient with acute lymphoblastic leukemia

artículo científico publicado en 2009

An Unusual Presentation of Carney Complex

artículo científico publicado en 2019

An infant with chronic hemolytic anemia.

artículo científico publicado en 2014

Analysis of Chromosomal Aberrations and FLT3 gene Mutations in Childhood Acute Myelogenous Leukemia Patients.

artículo científico publicado en 2012

Aplastic anemia presenting as hemophagocytic lymphohistiocytosis

artículo científico publicado en 2010

Approach to the patient with neutropenia in childhood

artículo científico publicado en 2015

Association between genetic polymorphism in DNA repair genes and risk of B-cell lymphoma.

artículo científico publicado en 2009

Blue toe syndrome--reply

artículo científico publicado en 2014

Chediak-higashi syndrome: a case report of a girl without silvery hair and oculocutaneous albinism presenting with hemophagocytic lymphohistiocytosis.

artículo científico publicado en 2014

Childhood mastocytosis: results of a single center.

artículo científico publicado en 2015

Clinical and laboratory data of primary hemophagocytic lymphohistiocytosis: A retrospective review of the Turkish Histiocyte Study Group.

artículo científico publicado en 2010

Coagulation Disturbances in Patients with Argininemia

scientific article published on 24 October 2018

Cytopenia associated with iron deficiency anemia and iron therapy: A report of two cases

scientific article published on 01 September 2011

DNA Repair Gene Polymorphisms and Their Relation With DNA Damage, DNA Repair, and Total Antioxidant Capacity in Childhood Acute Lymphoblastic Leukemia Survivors

artículo científico publicado en 2015

Deregulated WNT signaling in childhood T-cell acute lymphoblastic leukemia.

artículo científico

Effect of Prothrombotic Mutations on Factor Consumption in Children With Hemophilia ⬇️

artículo científico publicado el 12 de marzo de 2012

Erythrocyte membrane protein defects in hereditary spherocytosis patients in Turkish population.

artículo científico publicado en 2012

Evaluation of Alpha-Thalassemia Mutations in Cases with Hypochromic Microcytic Anemia: The İstanbul Perspective.

artículo científico publicado en 2015

Evaluation of PAX5 gene in the early stages of leukemic B cells in the childhood B cell acute lymphoblastic leukemia.

artículo científico publicado en 2011

Evaluation of high-risk features of primary enucleation of patients with retinoblastoma in a tertiary center of a developing country in the era of intra-arterial chemotherapy

artículo científico publicado en 2017

Febrile neutropenia in children with acute lymphoblastic leukemia: single center experience

artículo científico publicado en 2016

Five-year-old girl with tongue bleeding

artículo científico publicado en 2016

Frequency of ALK and GD2 Expression in Neuroblastoma

scientific article published on 07 April 2019

Hematological and biochemical changes in volatile substance abusing street children in İstanbul

Hemoglobin H Disease in Turkey: Experience from Eight Centers

artículo científico publicado en 2015

Hepatosplenic Fungal Infections in Children With Leukemia-Risk Factors and Outcome: A Multicentric Study

scientific article published on 01 May 2019

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

scientific article published on 19 July 2019

Homozygous protein C deficiency presenting as neonatal purpura fulminans: management with fresh frozen plasma, low molecular weight heparin and protein C concentrate

artículo científico publicado en 2017

Initial Management of Childhood Acute Immune Thrombocytopenia: Single-Center Experience of 32 Years.

artículo científico publicado en 2015

Juvenile Myelomonocytic Leukemia in Turkey: A Retrospective Analysis of 65 Patients

artículo científico publicado en 2017

Langerhans Cell Histiocytosis: Single Center Experience of 25 Years

scientific article published on 01 May 2019

Late effects of childhood ALL treatment on body mass index and serum leptin levels.

artículo científico publicado en 2010

Ligneous gingivitis: Hard to diagnose and treat

artículo científico publicado en 2019

Macrocephaly-Capillary Malformation Syndrome in a Newborn With Tetralogy of Fallot and Sagittal Sinus Thrombosis ⬇️

artículo científico publicado el 25 de marzo de 2012

Malignancy-associated hemophagocytic lymphohistiocytosis in pediatric cases: a multicenter study from Turkey.

artículo científico publicado en 2009

Malignancy-associated hemophagocytosis in children

Malignant rhabdoid tumor of the orbit

artículo científico publicado en 2013

Niemann-Pick disease

scientific article published on 01 March 2011

Non-Hodgkin's lymphoma in a hemophilic patient with a traumatic hematoma.

artículo científico publicado en 2011

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

artículo científico publicado en 2016

Novel use of propranolol for management of pain in children with vertebral hemangioma: report of two cases.

artículo científico publicado en 2013

PTEN and AKT1 Variations in Childhood T-cell Acute Lymphoblastic Leukemia

artículo científico publicado en 2019

Pediatric Stroke: A Single-Center Experience

scientific article published on 01 October 2019

Plasminogen deficiency

artículo científico publicado en 2017

Posterior reversible encephalopathy syndrome in children with acute lymphoblastic leukemia: Experience of a single center using BFM protocols

artículo científico publicado en 2019

Prenatal unilateral cerebellar hypoplasia diagnosed as PHACE syndrome.

artículo científico publicado en 2016

Prognostic gene alterations and clonal changes in childhood B-ALL

scientific article published on 08 June 2019

Prognostic significance of NOTCH1 and FBXW7 mutations in pediatric T-ALL ⬇️

artículo científico publicado el 1 de enero de 2010

Rare coagulation disorders: a retrospective analysis of 156 patients in Turkey.

artículo científico publicado en 2012

Reduced early prophylaxis of children with haemophilia in a developing country, Turkey ⬇️

artículo científico publicado el 20 de junio de 2011

Role of glutathione S-transferase M1, T1 and P1 gene polymorphisms in childhood acute lymphoblastic leukemia susceptibility in a Turkish population.

artículo científico publicado en 2015

Sinusoidal Obstruction Syndrome During Chemotherapy of Pediatric Cancers and its Successful Management With Defibrotide

artículo científico publicado en 2017

Sirolimus Experience in Blue Rubber Bleb Nevus Syndrome.

artículo científico publicado en 2017

Spontaneous intracranial bleeding in a neonate with congenital afibrinogenemia

artículo científico publicado en 2010

Spontaneous splenic rupture in a patient with congenital afibrinogenemia.

artículo científico publicado en 2014

Successful management of hepatic mucormycosis in an acute lymphoblastic leukaemia patient: a case report and review of the literature.

artículo científico

The Role of Epstein-Barr Virus LMP-1 Immunohistochemical Staining in Childhood Hodgkin Lymphoma.

artículo científico publicado en 2015

Thrombosis in children: Which test to whom, when and how much necessary?

scientific article published on 01 March 2018

Treatment of pediatric Burkitt lymphoma in Turkey.

artículo científico publicado en 2010

Treatment of plasminogen deficiency patients with fresh frozen plasma.

artículo científico publicado en 2017

Two acute myeloblastic leukemia cases concomitant with hemophagocytic lymphohistiocytosis and review of the literature.

artículo científico publicado en 2013

Upregulation of T-Cell-Specific Transcription Factor Expression in Pediatric T-Cell Acute Lymphoblastic Leukemia (T-ALL).

artículo científico publicado en 2012

Use of a High-Purity Factor X Concentrate in Turkish Subjects with Hereditary Factor X Deficiency: Post Hoc Cohort Subanalysis of a Phase 3 Study.

artículo científico publicado en 2018

Voriconazole induced bradycardia.

artículo científico publicado en 2013

Wernicke's Encephalopathy in a Child with Acute Lymphoblastic Leukemia.

artículo científico publicado en 2016

Lista de obras de

A 17-year experience with ALL-BFM protocol in acute lymphoblastic leukemia: prognostic predictors and interruptions during protocol.

A Case with Gaucher-Like Cells

A Case with Micromegakaryocytes

A Possible Role for WNT5A Hypermethylation in Pediatric Acute Lymphoblastic Leukemia.

A child presenting with hypercalcemia.

A new family with hereditary hyperferritinemia cataract syndrome

A novel combined treatment for plasminogen deficiency with lung involvement

A rare cause of thrombocyte dysfunction: Hermansky-Pudlak syndrome

Accidental High-dose Intrathecal Treatment: Late Results of a Patient

Adrenal masses in children: Imaging, surgical treatment and outcome

Alcaligenes xylosoxidans bacteremia in a patient with acute lymphoblastic leukemia

An Unusual Presentation of Carney Complex

An infant with chronic hemolytic anemia.

Analysis of Chromosomal Aberrations and FLT3 gene Mutations in Childhood Acute Myelogenous Leukemia Patients.

Aplastic anemia presenting as hemophagocytic lymphohistiocytosis

Approach to the patient with neutropenia in childhood

Association between genetic polymorphism in DNA repair genes and risk of B-cell lymphoma.

Blue toe syndrome--reply

Chediak-higashi syndrome: a case report of a girl without silvery hair and oculocutaneous albinism presenting with hemophagocytic lymphohistiocytosis.

Childhood mastocytosis: results of a single center.

Clinical and laboratory data of primary hemophagocytic lymphohistiocytosis: A retrospective review of the Turkish Histiocyte Study Group.

Coagulation Disturbances in Patients with Argininemia

Cytopenia associated with iron deficiency anemia and iron therapy: A report of two cases

DNA Repair Gene Polymorphisms and Their Relation With DNA Damage, DNA Repair, and Total Antioxidant Capacity in Childhood Acute Lymphoblastic Leukemia Survivors

Deregulated WNT signaling in childhood T-cell acute lymphoblastic leukemia.

Effect of Prothrombotic Mutations on Factor Consumption in Children With Hemophilia ⬇️

Erythrocyte membrane protein defects in hereditary spherocytosis patients in Turkish population.

Evaluation of Alpha-Thalassemia Mutations in Cases with Hypochromic Microcytic Anemia: The İstanbul Perspective.

Evaluation of PAX5 gene in the early stages of leukemic B cells in the childhood B cell acute lymphoblastic leukemia.

Evaluation of high-risk features of primary enucleation of patients with retinoblastoma in a tertiary center of a developing country in the era of intra-arterial chemotherapy

Febrile neutropenia in children with acute lymphoblastic leukemia: single center experience

Five-year-old girl with tongue bleeding

Frequency of ALK and GD2 Expression in Neuroblastoma

Hematological and biochemical changes in volatile substance abusing street children in İstanbul

Hemoglobin H Disease in Turkey: Experience from Eight Centers

Hepatosplenic Fungal Infections in Children With Leukemia-Risk Factors and Outcome: A Multicentric Study

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 protein C deficiency presenting as neonatal purpura fulminans: management with fresh frozen plasma, low molecular weight heparin and protein C concentrate

Initial Management of Childhood Acute Immune Thrombocytopenia: Single-Center Experience of 32 Years.

Juvenile Myelomonocytic Leukemia in Turkey: A Retrospective Analysis of 65 Patients

Langerhans Cell Histiocytosis: Single Center Experience of 25 Years

Late effects of childhood ALL treatment on body mass index and serum leptin levels.

Ligneous gingivitis: Hard to diagnose and treat

Macrocephaly-Capillary Malformation Syndrome in a Newborn With Tetralogy of Fallot and Sagittal Sinus Thrombosis ⬇️

Malignancy-associated hemophagocytic lymphohistiocytosis in pediatric cases: a multicenter study from Turkey.

Malignancy-associated hemophagocytosis in children

Malignant rhabdoid tumor of the orbit

Niemann-Pick disease

Non-Hodgkin's lymphoma in a hemophilic patient with a traumatic hematoma.

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

Novel use of propranolol for management of pain in children with vertebral hemangioma: report of two cases.

PTEN and AKT1 Variations in Childhood T-cell Acute Lymphoblastic Leukemia

Pediatric Stroke: A Single-Center Experience

Plasminogen deficiency

Posterior reversible encephalopathy syndrome in children with acute lymphoblastic leukemia: Experience of a single center using BFM protocols

Prenatal unilateral cerebellar hypoplasia diagnosed as PHACE syndrome.

Prognostic gene alterations and clonal changes in childhood B-ALL

Prognostic significance of NOTCH1 and FBXW7 mutations in pediatric T-ALL ⬇️

Rare coagulation disorders: a retrospective analysis of 156 patients in Turkey.

Reduced early prophylaxis of children with haemophilia in a developing country, Turkey ⬇️

Role of glutathione S-transferase M1, T1 and P1 gene polymorphisms in childhood acute lymphoblastic leukemia susceptibility in a Turkish population.

Sinusoidal Obstruction Syndrome During Chemotherapy of Pediatric Cancers and its Successful Management With Defibrotide

Sirolimus Experience in Blue Rubber Bleb Nevus Syndrome.

Spontaneous intracranial bleeding in a neonate with congenital afibrinogenemia

Spontaneous splenic rupture in a patient with congenital afibrinogenemia.

Successful management of hepatic mucormycosis in an acute lymphoblastic leukaemia patient: a case report and review of the literature.

The Role of Epstein-Barr Virus LMP-1 Immunohistochemical Staining in Childhood Hodgkin Lymphoma.

Thrombosis in children: Which test to whom, when and how much necessary?

Treatment of pediatric Burkitt lymphoma in Turkey.

Treatment of plasminogen deficiency patients with fresh frozen plasma.

Two acute myeloblastic leukemia cases concomitant with hemophagocytic lymphohistiocytosis and review of the literature.

Upregulation of T-Cell-Specific Transcription Factor Expression in Pediatric T-Cell Acute Lymphoblastic Leukemia (T-ALL).

Use of a High-Purity Factor X Concentrate in Turkish Subjects with Hereditary Factor X Deficiency: Post Hoc Cohort Subanalysis of a Phase 3 Study.

Voriconazole induced bradycardia.

Wernicke's Encephalopathy in a Child with Acute Lymphoblastic Leukemia.