Zobrazeno 1 - 10
of 156
pro vyhledávání: '"Intestinal ulcers"'
Autor:
Cheng-cheng Hou, Dan Luo, Hua-fang Bao, Jing-fen Ye, Hai-fen Ma, Yan Shen, Jun Zou, Jian-long Guan
Publikováno v:
Arthritis Research & Therapy, Vol 24, Iss 1, Pp 1-10 (2022)
Abstract Background Behçet’s syndrome (BS) is a rare variant vasculitis which can involve the eyes and gastrointestinal systems. However, ocular involvement rarely overlaps with intestinal lesions. This study aimed to compare the clinical characte
Externí odkaz:
https://doaj.org/article/790b4fd958ef472aa85a308748fe6478
Autor:
Xiaofen Zhang, Meng Jin, Zhe Shen, Xingyong Wan, Lan Li, Yuwei Zhang, Xinping Zhou, Chen Mei, Hongyan Tong, Chaohui Yu
Publikováno v:
BMC Gastroenterology, Vol 21, Iss 1, Pp 1-5 (2021)
Abstract Background Trisomy 8 positivity myelodysplastic syndrome with Behçet's disease is rare. Isolated trisomy 8 is a frequent cytogenetic abnormality in the MDS, but the characteristic of trisomy 8 and the association between trisomy 8 positivit
Externí odkaz:
https://doaj.org/article/41acb89938ef4087971f01b8c012d6ff
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-10 (2021)
Abstract Background Intestinal Behçet’s syndrome (BS) has high morbidity and mortality rates with serious complications. The purpose of this study was to investigate the clinical characteristics and laboratory parameters of intestinal and mucocuta
Externí odkaz:
https://doaj.org/article/f445b6c8b3af4490b9b10a60df549686
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-8 (2019)
Abstract Background Adamantiades-Behçet’s Disease (ABD) is an immunological recurrent systemic vasculitis with a chronic course. We investigated the predictors of long-term flare-ups, poor outcomes and event-free survival in Chinese non-surgical p
Externí odkaz:
https://doaj.org/article/c4e98079f0cb404d9bb0e7f685f6d1d4
Publikováno v:
Терапевтический архив, Vol 91, Iss 5, Pp 111-119 (2019)
Behçet's disease (BD) is a systemic vasculitis of unknown origin, characterized by recurrences of the ulcerative process in the oral cavity and on the genitals, inflammatory damage of the eyes, joints, vessels and other organs. The severity and prog
Externí odkaz:
https://doaj.org/article/afc0d4df9a6e4a5a8eee294387abcf3e
Autor:
R. G. Goloeva, Z. S. Alekberova
Publikováno v:
Научно-практическая ревматология, Vol 56, Iss 6, Pp 767-776 (2019)
Behсet's disease (BD) is a systemic vasculitis of an unknown etiology characterized by repeated oral and genital ulcerations and involvement of the eyes, joints, blood vessels, and other organs. In BD, it is the organ pathology that determines the s
Externí odkaz:
https://doaj.org/article/005386bb591a49469fe0c18669886d8f
Publikováno v:
Hygiene and sanitation. 100:568-579
Introduction. Due to the long-term radioactive contamination of a part of the territory of the Chelyabinsk region, much attention is paid to the analysis of the health status of the population. One of the adverse effects of radiation is the occurrenc
Publikováno v:
Indian Journal of Rheumatology, Vol 16, Iss 4, Pp 456-459 (2021)
Deficiency of adenosine deaminase 2 (DADA2) is a recently identified monogenic systemic inflammatory vasculopathy with variable clinical phenotype. The majority of reported patients are in pediatric age group. In this case report, we present a case o
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.