Results 321 to 330 of about 62,620 (348)
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Primary sclerosing cholangitis

Clinics in Liver Disease, 2004
Primary sclerosing cholangitis is a cholestatic liver disease strongly associated with IBD. Considerable advances in the understanding of its pathogenesis have been made. The idea of autoimmunity affecting genetically susceptible individuals is largely accepted; however, much remains to be explained about the origin of this disease.
Flavia D, Mendes, Keith D, Lindor
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Primary Sclerosing Cholangitis

Clinics in Liver Disease, 2013
Primary sclerosing cholangitis (PSC) is a chronic, progressive, cholestatic liver disease characterized by multifocal strictures of intra and extrahepatic bile ducts. PSC occurs more commonly in men and is often associated with inflammatory bowel disease. At present, there is no effective medical therapy for PSC. Current management of patients with PSC
Gideon M, Hirschfield   +3 more
openaire   +4 more sources

Primary Sclerosing Cholangitis

Surgical Clinics of North America, 1981
In spite of an improved understanding of the etiology of primary sclerosing cholangitis, which supports the use of immunosuppressive therapy with steroids and azathioprine, these pharmacologic manipulations have not altered the ultimate outcome of the disease. Drainage remains the most accepted mode of therapy when possible.
L F, Williams, D J, Schoetz
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Primary Sclerosing Cholangitis

Archives of Surgery, 1974
Three patients with primary sclerosing cholangitis confirmed by histologic examination were treated successfully with prolonged (three to six months) common duct drainage. No steroids or antibiotics were used. They are alive 14, 5, and 1½ years postoperatively.
M A, Oviedo, D, Volkmer, E F, Scanlon
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Primary Sclerosing Cholangitis

Archives of Internal Medicine, 1965
Mr. A is 32 years old. He was diagnosed with ulcerative colitis at the age 19 and is managed with five ASAs. He sees his IBD specialist on a yearly basis. His last colonoscopy was 3 years ago. At his last appointment, he was found to have abnormal liver biochemistry (bilirubin 23, alkaline phosphatase (ALP) 243, ALT 65, AST 72, gamma glutamyl ...
J G, MANESIS, J F, SULLIVAN
openaire   +2 more sources

Increase trend in the prevalence and male‐to‐female ratio of primary biliary cholangitis, autoimmune hepatitis, and primary sclerosing cholangitis in Japan

Hepatology Research, 2019
Autoimmune liver diseases (AILD) including autoimmune hepatitis (AIH), primary biliary cholangitis (PBC), and primary sclerosing cholangitis (PSC) impose a significant burden on public health, and it is important to estimate their prevalence.
A. Tanaka   +5 more
semanticscholar   +1 more source

Pediatric primary sclerosing cholangitis

Digestive Diseases and Sciences, 1986
An 11-year-old male presented with abdominal pain and emesis. Serum chemistries revealed cholestasis and an ERCP demonstrated sclerosing cholangitis. Secondary causes of this disease process were excluded. Sclerosing cholangitis is distinctly uncommon in the pediatric age group, but it should be considered in evaluation of patients of any age with ...
D A, Johnson, E L, Cattau, J E, Hancock
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Primary Sclerosing Cholangitis

Journal of Computer Assisted Tomography, 1983
Computed tomographic (CT) findings in six cases of primary sclerosing cholangitis (PSC) are described. Computed tomographic findings correlate with cholangiographic findings and show ductal dilatations and distortions in the porta hepatis and in the liver parenchyma.
A E, Ament   +4 more
openaire   +2 more sources

Reporting standards for primary sclerosing cholangitis using MRI and MR cholangiopancreatography: guidelines from MR Working Group of the International Primary Sclerosing Cholangitis Study Group

European Radiology, 2021
S. Venkatesh   +11 more
semanticscholar   +1 more source

Primary Biliary Cholangitis and Primary Sclerosing Cholangitis

American Journal of Gastroenterology, 2019
Cholestatic liver diseases encompass a broad spectrum of pathologies, with the core injury occurring at the level of cholangiocytes and progressing to hepatic fibrosis and liver dysfunction. Primary biliary cholangitis and primary sclerosing cholangitis are the most significant progressive cholangiopathies in adults. Although rare, they commonly evolve
Raquel T, Yokoda, Elizabeth J, Carey
openaire   +2 more sources

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