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Spectrum and clinical implications of syntaxin 11 gene mutations in familial haemophagocytic lymphohistiocytosis: association with disease-free remissions and haematopoietic malignancies

Journal of medical genetics, 2006-04, Vol.43 (4), p.e14-e14

2006

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Importance of RDW value in differential diagnosis of hypochrome anemias

American journal of hematology, 2002-01, Vol.69 (1), p.31-33

2002

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Diffusion-Weighted Cranial MR Imaging Findings in a Patient with Hemophagocytic Syndrome

American Journal of Neuroradiology, 2006-06, Vol.27 (6), p.1312-1314

2006

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Human MLH1 deficiency predisposes to hematological malignancy and neurofibromatosis type 1

Cancer research (Chicago, Ill.), 1999-01, Vol.59 (2), p.290-293

1999

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Spectrum, and clinical and functional implications of UNC13D mutations in familial haemophagocytic lymphohistiocytosis

Journal of medical genetics, 2008-03, Vol.45 (3), p.134-141

2008

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Congenital erythropoietic porphyria successfully treated by allogeneic bone marrow transplantation

Blood, 1998-12, Vol.92 (11), p.4053-4058

1998

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Benefit of high-dose methylprednisolone in comparison with conventional-dose prednisolone during remission induction therapy in childhood acute lymphoblastic leukemia for long-term follow-up

Leukemia, 2003-02, Vol.17 (2), p.328-333

2003

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The prevalence of factor V Leiden (1691 G-->A) mutation in Turkey

Turkish journal of pediatrics, 1997-07, Vol.39 (3), p.313

1997

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Prevalence of PAI‐1 gene 4G/5G genotype in Azerbaijan and Kyrgyzstan populations: literature review

Journal of thrombosis and haemostasis, 2003-04, Vol.1 (4), p.858-859

2003

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Congenital Erythropoietic Porphyria Successfully Treated by Allogeneic Bone Marrow Transplantation

Blood, 1998-12, Vol.92 (11), p.4053-4058

1998

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High frequency of thrombophilic disorders in women with recurrent fetal miscarriage

Clinical and experimental obstetrics & gynecology, 2006, Vol.33 (1), p.50-54

2006

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Sequencing of the factor 8(F8) coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations, and one rediagnosis of von Willebrand's disease type 2N

Haemophilia : the official journal of the World Federation of Hemophilia, 2006-07, Vol.12 (4), p.398-400

2006

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Endothelin 1 concentrations in infants with meconium stained amniotic fluid

Archives of disease in childhood. Fetal and neonatal edition, 2002-11, Vol.87 (3), p.F212-213

2002

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Primary Hemophagocytic Lymphohistiocytosis in Turkish Children

Pediatric hematology and oncology, 2003, Vol.20 (5), p.367-371

2003

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Two common genetic thrombotic risk factors: Factor V Leiden and prothrombin G20210A in adult Turkish patients with thrombosis

American journal of hematology, 2001-06, Vol.67 (2), p.107-111

2001

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The Effect of Hydroxyurea on the Coagulation System in Sickle Cell Anemia and β-Thalassemia Intermedia Patients: A Preliminary Study

Pediatric hematology and oncology, 2003, Vol.20 (6), p.429-434

2003

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Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Turkey

Haematologica (Roma), 2000-03, Vol.85 (3), p.320

2000

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Spectrum of Perforin Gene Mutations in Familial Hemophagocytic Lymphohistiocytosis

American journal of human genetics, 2001-03, Vol.68 (3), p.590-597

2001

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Thrombosis in children with cardiac pathology: frequency of factor V Leiden and prothrombin G20210A mutations

Pediatric cardiology, 2003-05, Vol.24 (3), p.244-248

2003

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The role of natural anticoagulant deficiencies and factor V Leiden in the development of idiopathic portal vein thrombosis

Journal of clinical gastroenterology, 2000-01, Vol.30 (1), p.66-71

2000

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Factor V Leiden mutation in patients with Behçet's disease

Journal of rheumatology, 1998-03, Vol.25 (3), p.496

1998

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Efficacy of FEIBA for acute bleeding and surgical haemostasis in haemophilia A patients with inhibitors: a multicentre registry in Turkey

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-05, Vol.18 (3), p.383-391

2012

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The factor V Leiden and prothrombin G20210A mutations in Kirghiz population

Thrombosis and haemostasis, 2000-08, Vol.84 (2), p.356-356

2000

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Prevalence of factor V Leiden and methylenetetrahydrofolate reductase C677T mutations in Azerbaijan

Thrombosis and haemostasis, 1998-09, Vol.80 (3), p.520-521

1998

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Prothrombin gene 20210 G‐A mutation in Turkish patients with thrombosis

American journal of hematology, 1998-10, Vol.59 (2), p.179-180

1998

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Spectrum and clinical implications of syntaxin 11 gene mutations in familial haemophagocytic lymphohistiocytosis: association with disease-free remissions and haematopoietic malignancies

Importance of RDW value in differential diagnosis of hypochrome anemias

Diffusion-Weighted Cranial MR Imaging Findings in a Patient with Hemophagocytic Syndrome

Human MLH1 deficiency predisposes to hematological malignancy and neurofibromatosis type 1

Spectrum, and clinical and functional implications of UNC13D mutations in familial haemophagocytic lymphohistiocytosis

Congenital erythropoietic porphyria successfully treated by allogeneic bone marrow transplantation

Benefit of high-dose methylprednisolone in comparison with conventional-dose prednisolone during remission induction therapy in childhood acute lymphoblastic leukemia for long-term follow-up

The prevalence of factor V Leiden (1691 G-->A) mutation in Turkey

Prevalence of PAI‐1 gene 4G/5G genotype in Azerbaijan and Kyrgyzstan populations: literature review

Congenital Erythropoietic Porphyria Successfully Treated by Allogeneic Bone Marrow Transplantation

High frequency of thrombophilic disorders in women with recurrent fetal miscarriage

Sequencing of the factor 8(F8) coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations, and one rediagnosis of von Willebrand's disease type 2N

Endothelin 1 concentrations in infants with meconium stained amniotic fluid

Primary Hemophagocytic Lymphohistiocytosis in Turkish Children

Two common genetic thrombotic risk factors: Factor V Leiden and prothrombin G20210A in adult Turkish patients with thrombosis

The Effect of Hydroxyurea on the Coagulation System in Sickle Cell Anemia and β-Thalassemia Intermedia Patients: A Preliminary Study

Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in Turkey

Spectrum of Perforin Gene Mutations in Familial Hemophagocytic Lymphohistiocytosis

Thrombosis in children with cardiac pathology: frequency of factor V Leiden and prothrombin G20210A mutations

The role of natural anticoagulant deficiencies and factor V Leiden in the development of idiopathic portal vein thrombosis

Factor V Leiden mutation in patients with Behçet's disease

Efficacy of FEIBA for acute bleeding and surgical haemostasis in haemophilia A patients with inhibitors: a multicentre registry in Turkey

The factor V Leiden and prothrombin G20210A mutations in Kirghiz population

Prevalence of factor V Leiden and methylenetetrahydrofolate reductase C677T mutations in Azerbaijan

Prothrombin gene 20210 G‐A mutation in Turkish patients with thrombosis

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