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The effect of depression, BDNF gene val66met polymorphism and gender on serum BDNF levels

Brain research bulletin, 2010-01, Vol.81 (1), p.61-65

2010

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Both Granulocytic and Non-Granulocytic Blood Cells Are Affected in Patients with Severe Congenital Neutropenia and Their Non-Neutropenic Family Members: An Evaluation of Morphology, Function, and Cell Death

Turkish journal of haematology, 2018, Vol.35 (4), p.229-259

2018

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Plasminogen Activator Inhibitor I 4G/5G Polymorphism in Neonatal Respiratory Distress Syndrome

Clinical and applied thrombosis/hemostasis, 2011-08, Vol.17 (4), p.352-357

2011

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Effects of Prophylactic Thyroid Hormone Replacement in Euthyroid Hashimoto's Thyroiditis

Endocrine Journal, 2005, Vol.52(3), pp.337-343

2005

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ALX4 dysfunction disrupts craniofacial and epidermal development

Human molecular genetics, 2009-11, Vol.18 (22), p.4357-4366

2009

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Cytotoxic effects of etephon and maleic hydrazide in Vero, Hep2, HepG2 cells

Drug and chemical toxicology (New York, N.Y. 1978), 2014-10, Vol.37 (4), p.459-465

2014

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The frequency of A91V in the perforin gene and the effect of tumor necrosis factor-α promoter polymorphism on acquired hemophagocytic lymphohistiocytosis

Turkish journal of haematology, 2011-06, Vol.28 (2), p.125-130

2011

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P3.03-052 Diagnostic Utility of Mesothelin, Osteopontin and Megakaryocyte Potentiation Factor in Turkish Patients with Malignant Mesothelioma

Journal of thoracic oncology, 2017-01, Vol.12 (1), p.S1377-S1378

2017

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P3.03-052 Diagnostic Utility of Mesothelin, Osteopontin and Megakaryocyte Potentiation Factor in Turkish Patients with Malignant Mesothelioma: Topic: Mesothelioma Clinical

Journal of thoracic oncology, 2017-01, Vol.12 (1), p.S1377-S1378

2017

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Transient depletion of innate immunity in varicella infections in otherwise healthy children

Turkish journal of haematology, 2009-03, Vol.26 (1), p.12-16

2009

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Recurrent macrophage activation syndrome associated with heterozygous perforin W374X gene mutation in a child with systemic juvenile idiopathic arthritis

Journal of pediatric hematology/oncology, 2013-07, Vol.35 (5), p.e205-e208

2013

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Smaller Hippocampus Volume Is Associated with Short Variant of 5-HTTLPR Polymorphism in Medication-Free Major Depressive Disorder Patients

Neuropsychobiology, 2011-01, Vol.63 (1), p.22-28

2011

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Neonatal primary hemophagocytic lymphohistiocytosis in Turkish children

Journal of pediatric hematology/oncology, 2008-12, Vol.30 (12), p.871-876

2008

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Omeprazole Inhibits Natural Killer Cell Functions

Digestive diseases and sciences, 2008-02, Vol.53 (2), p.347-351

2008

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Clinical and molecular aspects of Turkish familial hemophagocytic lymphohistiocytosis patients with perforin mutations

Leukemia research, 2008-06, Vol.32 (6), p.972-975

2008

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The First Report of a Homozygous Codons 9/10 (+T) β-Thalassemia Mutation in a Turkish Patient

Hemoglobin, 2015-01, Vol.39 (1), p.66-68

2015

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Assessment of clinical and laboratory presentations of familial hemophagocytic lymphohistiocytosis patients with homozygous W374X mutation

Leukemia research, 2010-08, Vol.34 (8), p.1012-1017

2010

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Possible Perforin-Munc13-4 Gene-Gene Interaction in Familial Hemophagocytic Lymphohistiocytosis

Blood, 2008-11, Vol.112 (11), p.4643-4643

2008

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Placental fas/fas ligand expression in early pregnancy losses

American journal of reproductive immunology (1989), 2008-07, Vol.60 (1), p.1-7

2008

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ORIGINAL ARTICLE: Placental Fas/Fas Ligand Expression in Early Pregnancy Losses

American journal of reproductive immunology (1989), 2008-07, Vol.60 (1), p.1-7

2008

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Rapid cell senescence and apoptosis in lymphocytes and granulocytes and absence of GM-CSF receptor in congenital dysgranulopoietic neutropenia

Leukemia research, 2008-02, Vol.32 (2), p.235-242

2008

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Disease causing nature of homozygous missense, p.A523D, alteration in the perforin gene

Leukemia research, 2009-09, Vol.33 (9), p.e152-e153

2009

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Neutrophil CD64 expression in Behçet's disease

Journal of rheumatology, 2005-05, Vol.32 (5), p.849

2005

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Congenital dysgranulopoietic neutropenia

Pediatric Blood & Cancer, 2008-01, Vol.50 (1), p.115-119

2008

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Effect of short course high dose methylprednisolone on endothelin-1 and nitric oxide in children with acute lymphoblastic leukemia: a preliminary study

Annals of hematology, 2006-01, Vol.85 (1), p.55-57

2006

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The effect of depression, BDNF gene val66met polymorphism and gender on serum BDNF levels

Both Granulocytic and Non-Granulocytic Blood Cells Are Affected in Patients with Severe Congenital Neutropenia and Their Non-Neutropenic Family Members: An Evaluation of Morphology, Function, and Cell Death

Plasminogen Activator Inhibitor I 4G/5G Polymorphism in Neonatal Respiratory Distress Syndrome

Effects of Prophylactic Thyroid Hormone Replacement in Euthyroid Hashimoto's Thyroiditis

ALX4 dysfunction disrupts craniofacial and epidermal development

Cytotoxic effects of etephon and maleic hydrazide in Vero, Hep2, HepG2 cells

The frequency of A91V in the perforin gene and the effect of tumor necrosis factor-α promoter polymorphism on acquired hemophagocytic lymphohistiocytosis

P3.03-052 Diagnostic Utility of Mesothelin, Osteopontin and Megakaryocyte Potentiation Factor in Turkish Patients with Malignant Mesothelioma

P3.03-052 Diagnostic Utility of Mesothelin, Osteopontin and Megakaryocyte Potentiation Factor in Turkish Patients with Malignant Mesothelioma: Topic: Mesothelioma Clinical

Transient depletion of innate immunity in varicella infections in otherwise healthy children

Recurrent macrophage activation syndrome associated with heterozygous perforin W374X gene mutation in a child with systemic juvenile idiopathic arthritis

Smaller Hippocampus Volume Is Associated with Short Variant of 5-HTTLPR Polymorphism in Medication-Free Major Depressive Disorder Patients

Neonatal primary hemophagocytic lymphohistiocytosis in Turkish children

Omeprazole Inhibits Natural Killer Cell Functions

Clinical and molecular aspects of Turkish familial hemophagocytic lymphohistiocytosis patients with perforin mutations

The First Report of a Homozygous Codons 9/10 (+T) β-Thalassemia Mutation in a Turkish Patient

Assessment of clinical and laboratory presentations of familial hemophagocytic lymphohistiocytosis patients with homozygous W374X mutation

Possible Perforin-Munc13-4 Gene-Gene Interaction in Familial Hemophagocytic Lymphohistiocytosis

Placental fas/fas ligand expression in early pregnancy losses

ORIGINAL ARTICLE: Placental Fas/Fas Ligand Expression in Early Pregnancy Losses

Rapid cell senescence and apoptosis in lymphocytes and granulocytes and absence of GM-CSF receptor in congenital dysgranulopoietic neutropenia

Disease causing nature of homozygous missense, p.A523D, alteration in the perforin gene

Neutrophil CD64 expression in Behçet's disease

Congenital dysgranulopoietic neutropenia

Effect of short course high dose methylprednisolone on endothelin-1 and nitric oxide in children with acute lymphoblastic leukemia: a preliminary study

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