Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Bekir Torun"'
Autor:
Bekir Torun, Şükran Erten
Publikováno v:
Ulusal Romatoloji Dergisi, Vol 16, Iss 2, Pp 51-56 (2024)
Objective: The aim of this study is to determine of the frequency of osteoporosis in patient with non-radiographic axial spondyloarthritis (SpA) and ankylosing spondilitis. The correlation between frequency of osteoporosis and disease activity and se
Externí odkaz:
https://doaj.org/article/3613ec75337d44d39dac627912097698
Autor:
Gözde Yıldırım Çetin, Fatih Yıldız, Sezen Koçarslan, Fatih Albayrak, Bekir Torun, Burak Okyar
Publikováno v:
Cukurova Medical Journal, Vol 47, Iss 2, Pp 901-904 (2022)
Background: Mönckeberg Medial Calcific Sclerosis (MMCS) is a rare condition that can mimic giant cell arteritis (GCA). It may be misinterpreted as giant cell arteritis by the clinician and cause unnecessary treatments. Therefore, it is a disease tha
Externí odkaz:
https://doaj.org/article/6ea471d07c994c5b9fb3ee18e762a0e7
Publikováno v:
Modern Rheumatology Case Reports. 7:315-319
Werner syndrome (WS), also known as adult progeria, is a premature ageing syndrome that can manifest itself with grey hair, hair loss, diabetes mellitus, hyperlipidaemia, hypertension, skin disorders, ocular cataracts, myocardial infarction, osteopor
Publikováno v:
Cukurova Medical Journal. 47:1761-1763
Behçet syndrome(BS), also known as Behçet disease (BD), is characterized by recurrent oral aphthae and any of several systemic manifestations including genital aphthae, ocular disease, skin lesions, gastrointestinal involvement, neurologic disease,
Autor:
Burak OKYAR, Bekir TORUN, Fatih ALBAYRAK, Sezen KOÇARSLAN, Fatih YILDIZ, Gözde YILDIRIM ÇETİN
Publikováno v:
Cukurova Medical Journal. 47:901-904
Background: Mönckeberg Medial Calcific Sclerosis (MMCS) is a rare condition that can mimic giant cell arteritis (GCA). It may be misinterpreted as giant cell arteritis by the clinician and cause unnecessary treatments. Therefore, it is a disease tha
Autor:
Burak Okyar, Bekir Torun, Esen Saba Öktem, Abdulkadir Yasir Bahar, Fatih Yıldız, Gözde Yıldırım Çetin
Publikováno v:
Modern Rheumatology Case Reports. 7:271-275
Castleman’s disease (CD) is a rare, systemic disease with histopathological features of angiofollicular lymph node hyperplasia. In the literature, there are case-level reports that mimic or coexist with systemic lupus erythematosus (SLE) clinically
Autor:
Burak Okyar, Nurhan Atilla, Fatih Albayrak, Bekir Torun, Gozde Yildirim Cetin, Betül Kizildağ, Fatih Yildiz
Publikováno v:
Volume: 5, Issue: 2 188-192
Journal of Surgery and Medicine
Journal of Surgery and Medicine, Vol 5, Iss 2, Pp 188-192 (2021)
Journal of Surgery and Medicine
Journal of Surgery and Medicine, Vol 5, Iss 2, Pp 188-192 (2021)
Systemic Sclerosis (SSc) is a multi-systemic connective tissue disease of unknown etiology. Although many pathological processes play a role in the basis of pulmonary hypertension (PHT) that develops secondary to SSc, vasculopathy has an important pl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::85cd9e829ba24b0c9c1f6ebd38555ece
https://dergipark.org.tr/tr/pub/josam/issue/60239/841679
https://dergipark.org.tr/tr/pub/josam/issue/60239/841679