Zobrazeno 1 - 8
of 8
pro vyhledávání: '"E A Arion"'
Publikováno v:
Терапевтический архив, Vol 84, Iss 8, Pp 86-90 (2012)
Primary sclerosing cholangitis (PSC) is a chronic slowly progressive cholestatic liver disease characterized by non-purulent destructive inflammation and sclerosis of the extra- and intrahepatic bile ducts, leading to secondary biliary cirrhosis. The
Externí odkaz:
https://doaj.org/article/d6f0b018b22b49ab982e1e8af14b45c7
Publikováno v:
Акушерство, гинекология и репродукция, Vol 5, Iss 4, Pp 6-8 (2016)
Primary sclerosing cholangitis (PSC) is autoimmune disease characterized by inflammation and sclerosis of the bile duct, which leads to the development of secondary biliary cirrhosis. Many women with primary sclerosing cholangitis are at reproductive
Externí odkaz:
https://doaj.org/article/d641fbd9429e4376a5a6bbe2dbed0e8f
Publikováno v:
Klinicheskaia meditsina. 94(1)
Wilson-Konovalov's disease is a rare genetic pathology of copper metabolism that in the first place affects liver and CNS. Due to autosomal-recessive inheritance of this condition, it most frequently occurs in sibs. We report a case of Wilson-Konoval
Publikováno v:
Klinicheskaia meditsina. 91(4)
Primary sclerosing cholangitis (PSC) is a chronic slowly developing cholestatic diseases of liver characterized by non-purulent destructive inflammation and fibrosis of bile ducts leading to secondary biliary cirrhosis. PSC etiology remains unknown a
Publikováno v:
Klinicheskaia meditsina. 91(3)
A case of a rare hereditary disease, Alagille-Watson syndrome, is reported. It most frequently affects liver and cardiovascular system which leads to biliary cirrhosis and cardiovascular catastrophe in young patients. Pathogenesis and clinical varian
Publikováno v:
Klinicheskaia meditsina. 91(1)
Two clinical observations of the variant form of hepatic lesion: autoimmune hepatitis--primary biliary cirrhosis with systemic manifestations are presented in patients with long-standing Sjogren's syndrome, one at the stage of lever cirrhosis, the ot
Publikováno v:
Klinicheskaia meditsina. 83(6)
Publikováno v:
Scopus-Elsevier
Wilson-Konovalov’s disease is a rare genetic pathology of copper metabolism that in the first place affects liver and CNS. Due to autosomal-recessive inheritance of this condition, it most frequently occurs in sibs. We report a case of Wilson-Konov
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b23a187e7aa0f41698ac8688496a06e2
http://www.scopus.com/inward/record.url?eid=2-s2.0-84974693330&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-84974693330&partnerID=MN8TOARS