Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Burak Okyar"'
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
Publikováno v:
Journal of Medicine and Palliative Care. 3:117-121
Although many mechanisms leading to lung fibrosis in systemic sclerosis-associated interstitial lung disease (SSc-ILD) have been suggested, this issue has not been fully understood yet. Recently, there has been increased evidence that the mediators a
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, Omer Karadag
Publikováno v:
Acta Medica. 52:70-112
Publikováno v:
Volume: 12, Issue: 3 760-764
Clinical and Experimental Health Sciences
Clinical and Experimental Health Sciences
Objective: Nailfold Videocapilloroscopy (NVC) is an examination method that is used as an aid in the diagnosis, follow-up, and treatment strategy of rheumatic diseases such as systemic sclerosis, systemic lupus erythematosus, rheumatoid arthritis, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c69bcdc080e5e4581875e46dc12556bc
https://dergipark.org.tr/tr/pub/clinexphealthsci/issue/72731/1022573
https://dergipark.org.tr/tr/pub/clinexphealthsci/issue/72731/1022573
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
Autor:
Cihan Yeşil, Burak Okyar
Publikováno v:
Cumhuriyet Medical Journal.
Tests used to diagnose Coronavirus Disease-2019 (COVID-19) disease; Polymerase Chain Reaction (PCR) test, Rapid Antibody Test (RAT) and Thorax Computed Tomography (CT) in patients with appropriate history, clinical and laboratory. The sensitivity of