Search Results - "Fahri ŞAHİN"

SURGICAL INTERVENTIONS IN FACTOR VII DEFICIENCY: A SINGLE CENTER EXPERIENCE by Betül Kübra TÜZÜN, Zühal DEMİRCİ, Bahar SEVGİLİ, Güray SAYDAM, Fahri ŞAHİN

“…Objective: FVII deficiency is the most common of the rare congenital bleeding disorders with a prevalence of about 1:500,000. Bleeding symptoms are…”
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Real-Life Experience with Pomalidomide plus Dexamethasone in Patients with Multiple Myeloma: A Single Center Retrospective Study by Betül Kübra TÜZÜN, Zühal DEMİRCİ, Gülçin ÇELEBİ, Ajda GÜNEŞ, Derya DEMİR, Nur SOYER, Filiz VURAL, Mahmut TÖBÜ, Fahri ŞAHİN, Güray SAYDAM

“…Objective: Multiple myeloma (MM) is a heterogeneous disease with the uncontrolled clonal proliferation of plasma cells, accounting for approximately 10% of all…”
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Hemophilia Patients’ Level of Knowledge of About Viral Hepatitis by PULLUKÇU, Hüsnü, Işıkgöz TAŞBAKAN, Meltem, ZEKA, Arzu Nazlı, YAMAZHAN, Tansu, DURUSOY, Raika, ŞAHİN, Fahri, SAYDAM, Güray

“…Introduction: Hemophilia is a genetic disease presenting predominantly with joint hemorrhages in clinical course. Thus, its treatment requires transfusion of…”
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The effect of malnutrition on mortality in hospitalized patients with hematologic malignancy by Yilmaz, Merve, Atilla, Fatos Dilan, Sahin, Fahri, Saydam, Guray

“…Objectives The aim of this study was to assess the association between malnutrition status with the (Global Leadership Initiative on Malnutrition) GLIM…”
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Accuracy and clinical role of digital templating for total knee arthroplasty performed on haemophilic knees by Vahabi, Arman, Er, Erdem, Biçer, Elcil Kaya, Şahin, Fahri, Kavakli, Kaan, Aydoğdu, Semih

“…Introduction In total knee arthroplasty (TKA), choosing the correct implant size is important. There is lack of data on accuracy of templating on haemophilic…”
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The assessment of health-related quality of life in patients with polycythemia vera by Doğan, Esma Evrim, Keklik Karadağ, Fatma, Aydin, Demet, Demirel, Naciye, Sağlam, Selin, Davulcu, Eren Arslan, Turan Erkek, Esra, Eren, Rafet, Akad Soyer, Nur, Şahin, Fahri, Saydam, Güray

“…Previous studies have shown that patients with polycythemia vera (PV) have poor quality of life (QoL). Similarly, it has been shown that survival is influenced…”
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Level of Awareness of Acquired Hemophilia A Among Physicians in Türkiye: A Survey Study by Demir, Ahmet Muzaffer, Ar, Muhlis Cem, Sahin, Fahri, Altunbaş, Merve

“…This survey study aimed to evaluate the level of awareness and knowledge of acquired hemophilia A (AHA) among physicians from various specialties. Data were…”
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Morphological analysis of patellofemoral joint in haemophilic arthropathy: A case‐control study by Vahabi, Arman, Biçer, Elcil Kaya, Kayıkçı, Kayahan, Şahin, Fahri, Kavaklı, Kaan, Tamsel, İpek, Aydoğdu, Semih

“…Introduction Knees affected by haemophilic arthropathy exhibit distinct differences in both bone morphology and soft tissue behaviour. This study aims to…”
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Depression and anxiety in patients with hemophilia A and B by Koseoglu, Fatos D, Zuhal, Demirci, Onen-Sertoz, Ozen, Fahri, Sahin

“…Objective This study described the prevalence of and correlates of depression and anxiety in adult patients with hemophilia A and B. Methods In this…”
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Incidental Diagnosis of Cyclic Thrombocytopenia: An Asymptomatic Case by Keklik Karadağ, Fatma, Gunes, Ajda, Mete Gokmen, Nihal, Şahin, Fahri, Saydam, Guray

“…Cyclic thrombocytopenia (CTP) is a very rare condition that is characterized by episodic thrombocytopenia over a period of three to five weeks. The…”
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CHARACTERIZATION AND MANAGEMENT OF PATIENTS WITH HEREDITARY FACTOR X DEFICIENCY: A RETROSPECTIVE SINGLE CENTER EXPERIENCE by Nigar Abdullayeva, Fahri Sahin, Zuhal Demirci, Bahar Sevgili

“…Objective: Factor X deficiency (FXd) is a rare coagulation disorder that can be either hereditary or acquired. Case report: We characterized patients with FXd…”
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Different clinical courses with the same findings: two cases of paroxysmal nocturnal hemoglobinuria presenting with thrombocytopenia by Karakuş, Volkan, Kaya, Egemen, Dere, Yelda, Şahin, Fahri

“…Paroxysmal nocturnal hemoglobinuria (PNH) is a clonal stem cell disease that manifests with chronic intravascular hemolysis, thrombosis, and bone marrow…”
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PB2652: EVALUATION OF 6 CASES WITH FXIII DEFICIENCY: SINGLE CENTRE EXPERIENCE by Sahin, Fahri, Bozer, Denis, Demirci, Zuhal, Saydam, Guray

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The value of ultrasonography in detecting early arthropathic changes and contribution to the clinical approach in patients of hemophilia by Tamsel, İpek, Kavakli, Kaan, Özbek, S. Süreyya, Hekimsoy, İlhan, Balkan, Can, Şahin, Fahri, Tamsel, Sadık

“…PURPOSE\AIM Hemophilia affects the blood clotting process, is a genetic disease characterized by recurrent bleeding. The hemophilia early arthropathy detection…”
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PB2645: HEMATURIA IN ADULT HAEMOPHILIC INDIVIDUALS: IS THE HEMAOPHILIA THE ONLY CAUSE OF HEMATURIA? A SINGLE CENTRE EXPERIENCE FOR A DECADE by Tüzün, Betül Kübra, Demirci, Zühal, Saydam, Güray, Şahin, Fahri

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Sleeve Gastrectomy in a Severe Hemophilia A Patient: One of the Very Rare Cases by Davulcu, Eren Arslan, Demirci, Zühal, Fırat, Özgür, Saydam, Güray, Şahin, Fahri

“…Obesity is becoming a problem for aging hemophilia patients. The estimated prevalence of overweight and obesity in European and North American hemophilia…”
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Management of Primary Immune Thrombocytopenia: Turkish Modified Delphi-Based Consensus Statement for Special Considerations by Ümit, Elif Gülsüm, Demir, Ahmet Muzaffer, Ar, Muhlis Cem, Ayer, Mesut, Aylı, Meltem, Karakuş, Volkan, Kaya, Emin, Özkalemkaş, Fahir, Sayınalp, Nilgün, Sönmez, Mehmet, Şahin, Fahri, Toprak, Selami Koçak, Toptaş, Tayfur, Yavaşoğlu, İrfan, Çalış, Ümran

“…Primary immune thrombocytopenia (ITP) is an acquired disorder of platelets with a complex and unclear mechanism of increased immune destruction or impaired…”
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Gene therapy in haemophilia: literature review and regional perspectives for Turkey by Kavaklı, Kaan, Antmen, Bülent, Okan, Vahap, Şahin, Fahri, Aytaç, Selin, Balkan, Can, Berber, Ergül, Kaya, Zühre, Küpesiz, Alphan, Zülfikar, Bülent

“…Haemophilia is an X-linked lifelong congenital bleeding disorder that is caused by insufficient levels of factor VIII (FVIII; haemophilia A) or factor IX (FIX;…”
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The roles of bioactive sphingolipids in resveratrol-induced apoptosis in HL60 acute myeloid leukemia cells by Cakir, Zeynep, Saydam, Guray, Sahin, Fahri, Baran, Yusuf

“…Purpose Acute promyelocytic leukemia results from a translocation between 15 and 17 chromosomes that produce PML/RARα fusion protein. PML/RARα inhibits…”
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Prevalence of anemia and malnutrition and their association in elderly nursing home residents by Sahin, Sevnaz, Tasar, Pinar Tosun, Simsek, Hatice, Çicek, Zeynep, Eskiizmirli, Hulya, Aykar, Fisun Senuzun, Sahin, Fahri, Akcicek, Fehmi

“…Purpose Malnutrition is one of the most important geriatric syndromes in the elderly. The aim of this study was to investigate the association between anemia…”
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