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Therapeutic plasma exchange in primary hemophagocytic lymphohistiocytosis: reports of two cases and a review of the literature

Transfusion and apheresis science, 2016-12, Vol.55 (3), p.353-356

2016

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Thiamine-responsive megaloblastic anemia syndrome

International journal of hematology, 2010-10, Vol.92 (3), p.524-526

2010

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Detection of Left Ventricular Regional Function in Asymptomatic Children with beta-Thalassemia Major by Longitudinal Strain and Strain Rate Imaging

Turkish journal of haematology, 2013-09, Vol.30 (3), p.283-289

2013

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Author Self-Citation in the Turkish Otorhinolaryngology Literature

Turkish archives of otolaryngology, 2021-09, Vol.59 (3), p.210-214

Bayram, Ali

2021

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Hemoglobin H Disease in Turkey: Experience from Eight Centers

Turkish journal of haematology, 2016-03, Vol.33 (1), p.56-59

2016

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Evaluation of the plasma micro RNA expression levels in secondary hemophagocytic lymphohistiocytosis

Mediterranean journal of hematology and infectious diseases, 2013-01, Vol.5 (1), p.e2013066-e2013066

2013

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IMPORTANCE OF HYPERBILURUBINEMIA IN DIFFERENTIATION OF PRIMARY AND SECONDARY HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS IN PEDIATRIC CASES

Mediterranean journal of hematology and infectious diseases, 2014-10, Vol.6 (1), p.e2014067-e2014067

2014

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Vincristine induced cranial polyneuropathy

Indian journal of pediatrics, 2006-06, Vol.73 (6), p.531-533

2006

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Conservative management of an acute spinal epidural hemorrhage in a child with hemophilia a with inhibitor

Blood coagulation & fibrinolysis, 2016-12, Vol.27 (8), p.930-932

2016

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A rare combination: congenital factor VII deficiency with Chiari malformation

Blood coagulation & fibrinolysis, 2015-12, Vol.26 (8), p.946-948

2015

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Prognostic Factors and Long-Term Outcome in 52 Turkish Children With Hemophagocytic Lymphohistiocytosis

Pediatric critical care medicine, 2015-07, Vol.16 (6), p.e165-e173

2015

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Newborn infant with hemophagocytic lymphohistiocytosis and generalized skin eruptions

Journal of dermatology, 2006-09, Vol.33 (9), p.628-631

2006

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Use of rituximab in chronic childhood immune thrombocytopenic purpura

Pediatrics international, 2006-10, Vol.48 (5), p.514-516

2006

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Plasma microRNA profiling of pediatric patients with immune thrombocytopenic purpura

Blood coagulation & fibrinolysis, 2014-06, Vol.25 (4), p.379-383

2014

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Granulocyte Transfusion Therapy in Childhood

Indian journal of hematology & blood transfusion, 2017-09, Vol.33 (3), p.417-420

2017

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Wiskott-Aldrich syndrome mutation in two Turkish siblings with X-linked thrombocytopenia

Turkish journal of haematology, 2011-06, Vol.28 (2), p.139-141

2011

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Primary Varicella Infection Associated with Stevens‐Johnson Syndrome in a Turkish Child

Journal of dermatology, 2005-09, Vol.32 (9), p.745-750

2005

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Thrombotic thrombocytopenic purpura concomitant with autoimmune thyroiditis

Dicle tıp dergisi, 2011-12, Vol.38 (4), p.503-506

Bay, Ali

2011

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Avian Influenza A (H5N1) Infection in Eastern Turkey in 2006

The New England journal of medicine, 2006-11, Vol.355 (21), p.2179-2185

2006

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Acute myeloblastic leukemia-associated Marfan syndrome and Davidoff-Dyke-Masson syndrome: a case report

Turkish journal of haematology, 2008-12, Vol.25 (4), p.198-200

2008

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Subtle differences in CTL cytotoxicity determine susceptibility to hemophagocytic lymphohistiocytosis in mice and humans with Chediak-Higashi syndrome

Blood, 2011-10, Vol.118 (17), p.4620-4629

2011

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

Turkish journal of haematology, 2010-12, Vol.27 (4), p.257-262

2010

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A case of immune thrombocytopenic purpura presenting with recurrent intracranial hemorrhage

Pediatrics international, 2005-02, Vol.47 (1), p.109-111

2005

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Refugee children with cancer in Turkey

The lancet oncology, 2016-07, Vol.17 (7), p.865-867

2016

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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

Pediatric blood & cancer, 2019-10, Vol.66 (10), p.e27923-n/a

2019

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Therapeutic plasma exchange in primary hemophagocytic lymphohistiocytosis: reports of two cases and a review of the literature

Thiamine-responsive megaloblastic anemia syndrome

Detection of Left Ventricular Regional Function in Asymptomatic Children with beta-Thalassemia Major by Longitudinal Strain and Strain Rate Imaging

Author Self-Citation in the Turkish Otorhinolaryngology Literature

Hemoglobin H Disease in Turkey: Experience from Eight Centers

Evaluation of the plasma micro RNA expression levels in secondary hemophagocytic lymphohistiocytosis

IMPORTANCE OF HYPERBILURUBINEMIA IN DIFFERENTIATION OF PRIMARY AND SECONDARY HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS IN PEDIATRIC CASES

Vincristine induced cranial polyneuropathy

Conservative management of an acute spinal epidural hemorrhage in a child with hemophilia a with inhibitor

A rare combination: congenital factor VII deficiency with Chiari malformation

Prognostic Factors and Long-Term Outcome in 52 Turkish Children With Hemophagocytic Lymphohistiocytosis

Newborn infant with hemophagocytic lymphohistiocytosis and generalized skin eruptions

Use of rituximab in chronic childhood immune thrombocytopenic purpura

Plasma microRNA profiling of pediatric patients with immune thrombocytopenic purpura

Granulocyte Transfusion Therapy in Childhood

Wiskott-Aldrich syndrome mutation in two Turkish siblings with X-linked thrombocytopenia

Primary Varicella Infection Associated with Stevens‐Johnson Syndrome in a Turkish Child

Thrombotic thrombocytopenic purpura concomitant with autoimmune thyroiditis

Avian Influenza A (H5N1) Infection in Eastern Turkey in 2006

Acute myeloblastic leukemia-associated Marfan syndrome and Davidoff-Dyke-Masson syndrome: a case report

Subtle differences in CTL cytotoxicity determine susceptibility to hemophagocytic lymphohistiocytosis in mice and humans with Chediak-Higashi syndrome

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

A case of immune thrombocytopenic purpura presenting with recurrent intracranial hemorrhage

Refugee children with cancer in Turkey

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

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