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Novel RUNX1 Variation in B-cell Acute Lymphoblastic Leukemia

Mediterranean journal of hematology and infectious diseases, 2023, Vol.15 (1), p.e2023036-e2023036

2023

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Prevalence of human papilloma virus types in Turkish and Albanian women

Journal of cytology, 2018-10, Vol.35 (4), p.252-254

2018

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A Novel ATP6V0A2 Mutation Causing Recessive Cutis Laxa with Unusual Manifestations of Bleeding Diathesis and Defective Wound Healing

Turkish journal of haematology, 2019-02, Vol.36 (1), p.29-36

2019

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Prognostic significance of carbonic anhydrase IX overexpression in stage III non-small cell lung cancer patients after neoadjuvant treatment

Pathology, research and practice, 2018-09, Vol.214 (9), p.1291-1296

2018

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Coronary Artery Ectasia Is Associated with the c.894G>T (Glu298Asp) Polymorphism of the Endothelial Nitric Oxide Synthase Gene

The Tohoku Journal of Experimental Medicine, 2014, Vol.232(2), pp.137-144

2014

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Neurologic involvement in atypical hemolytic uremic syndrome and successful treatment with eculizumab

Pediatric nephrology (Berlin, West), 2013-05, Vol.28 (5), p.827-830

2013

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The impact of platelet membrane glycoprotein Ib alpha and Ia/IIa polymorphisms on the risk of thrombosis in the antiphospholipid syndrome

Thrombosis research, 2012-04, Vol.129 (4), p.486-491

2012

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New Indicator of Cellular Ischemia in Coronary Slow Flow Phenomenon; Cell-Free DNA

Türk Kardiyoloji Derneği arşivi, 2020-09, Vol.48 (6), p.558-565

Yolcu, Mustafa

2020

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Beta 2 glycoprotein I Valine247Leucine polymorphism in patients with antiphospholipid syndrome

Experimental biomedical research, 2022-07, Vol.5 (3), p.293

2022

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The relationship between clinical parameters and hepatocyte growth factor/c-Met levels in the sperm of infertile males

Journal of men's health (Amsterdam), 2022-08, Vol.18 (8), p.1

2022

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Poisoning by butylated hydroxytoluene quinone methide acting as a superwarfarin: first reported case in humans

Blood coagulation & fibrinolysis, 2024-07, Vol.35 (5), p.279-281

2024

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Prophylactic Eculizumab Use in Kidney Transplantation: A Review of the Literature and Report of a Case with Atypical Hemolytic Uremic Syndrome

Annals of Transplantation, 2015-12, Vol.20, p.714-719

2015

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A Novel COL3A1 c.2644G>T; p.(Gly882Cys) Variant in a Turkish Family with Vascular Ehlers-Danlos Syndrome

Molecular syndromology, 2020-06, Vol.11 (2), p.110-114

2020

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Aberrant Activation-Induced Cytidine Deaminase Gene Expression Links BCR/ABL1-Negative Classical Myeloproliferative Neoplasms

Haseki tıp bülteni, 2022-06, Vol.60 (3), p.228-233

2022

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The First Congenital Disorders of Glycosylation Patient (Fetus) with Homozygous COG5 c.95T>G Variant

Molecular syndromology, 2023-04, Vol.14 (2), p.181-184

2023

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The Association Between Factor XIII Val34Leu Polymorphism and Early Myocardial Infarction

Circulation Journal, 2006, Vol.70(3), pp.239-242

2006

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Glycoprotein Ibα Kozak polymorphism in patients presenting with early-onset acute coronary syndrome

Archives of medical science, 2018-06, Vol.14 (4), p.788-793

2018

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A Novel Pathological ARSB Mutation (c.870G>A; p.Trp290stop) in Mucopolysaccharidosis Type VI Patients

Molecular syndromology, 2019-11, Vol.10 (5), p.272-275

2019

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A Novel Ganciclovir Resistance Mutation in the UL97 Gene of the HHV-5 in an Adult Hematopoietic Stem Cell Transplant Recipient

Future virology, 2017-12, Vol.12 (12), p.761-766

2017

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Two Rare Pathogenic HBB Variants in a Patient with β-Thalassemia Intermedia

Turkish journal of haematology, 2020-01, Vol.37 (2), p.135-136

2020

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Overexpression of Fc mu receptor (FCMR, TOSO) gene in chronic lymphocytic leukemia patients

Medical oncology (Northwood, London, England), 2012-06, Vol.29 (2), p.1068-1072

2012

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β Globin Mutations in Turkish, Northern Iraqi and Albanian Patients with β Thalassemia Major

Thalassemia reports, 2018-07, Vol.8 (2), p.7286

2018

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Three Factor 11 Mutations Associated with Factor XI Deficiency in a Turkish Family

Turkish journal of haematology, 2018-03, Vol.35 (1), p.79-80

2018

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Three Novel Calreticulin Mutations in Two Turkish Patients

Turkish journal of haematology, 2017-12, Vol.34 (4), p.360-361

2017

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The association of P-selectin glycoprotein ligand-1 VNTR polymorphisms with coronary stent restenosis

Journal of thrombosis and thrombolysis, 2007-06, Vol.23 (3), p.181-187

2007

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Novel RUNX1 Variation in B-cell Acute Lymphoblastic Leukemia

Prevalence of human papilloma virus types in Turkish and Albanian women

A Novel ATP6V0A2 Mutation Causing Recessive Cutis Laxa with Unusual Manifestations of Bleeding Diathesis and Defective Wound Healing

Prognostic significance of carbonic anhydrase IX overexpression in stage III non-small cell lung cancer patients after neoadjuvant treatment

Coronary Artery Ectasia Is Associated with the c.894G>T (Glu298Asp) Polymorphism of the Endothelial Nitric Oxide Synthase Gene

Neurologic involvement in atypical hemolytic uremic syndrome and successful treatment with eculizumab

The impact of platelet membrane glycoprotein Ib alpha and Ia/IIa polymorphisms on the risk of thrombosis in the antiphospholipid syndrome

New Indicator of Cellular Ischemia in Coronary Slow Flow Phenomenon; Cell-Free DNA

Beta 2 glycoprotein I Valine247Leucine polymorphism in patients with antiphospholipid syndrome

The relationship between clinical parameters and hepatocyte growth factor/c-Met levels in the sperm of infertile males

Poisoning by butylated hydroxytoluene quinone methide acting as a superwarfarin: first reported case in humans

Prophylactic Eculizumab Use in Kidney Transplantation: A Review of the Literature and Report of a Case with Atypical Hemolytic Uremic Syndrome

A Novel COL3A1 c.2644G>T; p.(Gly882Cys) Variant in a Turkish Family with Vascular Ehlers-Danlos Syndrome

Aberrant Activation-Induced Cytidine Deaminase Gene Expression Links BCR/ABL1-Negative Classical Myeloproliferative Neoplasms

The First Congenital Disorders of Glycosylation Patient (Fetus) with Homozygous COG5 c.95T>G Variant

The Association Between Factor XIII Val34Leu Polymorphism and Early Myocardial Infarction

Glycoprotein Ibα Kozak polymorphism in patients presenting with early-onset acute coronary syndrome

A Novel Pathological ARSB Mutation (c.870G>A; p.Trp290stop) in Mucopolysaccharidosis Type VI Patients

A Novel Ganciclovir Resistance Mutation in the UL97 Gene of the HHV-5 in an Adult Hematopoietic Stem Cell Transplant Recipient

Two Rare Pathogenic HBB Variants in a Patient with β-Thalassemia Intermedia

Overexpression of Fc mu receptor (FCMR, TOSO) gene in chronic lymphocytic leukemia patients

β Globin Mutations in Turkish, Northern Iraqi and Albanian Patients with β Thalassemia Major

Three Factor 11 Mutations Associated with Factor XI Deficiency in a Turkish Family

Three Novel Calreticulin Mutations in Two Turkish Patients

The association of P-selectin glycoprotein ligand-1 VNTR polymorphisms with coronary stent restenosis

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