Results 181 to 190 of about 94,453 (216)
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Pathogenesis of Biliary Atresia

Pediatrics, 1986
To the Editor.— The report of biliary atresia in one identical twin is of interest. As the authors' state, the observation suggests that the malformation may be acquired rather than of genetic origin. Many pediatric pathologists consider biliary atresia an acquired defect in a large, but unknown, proportion of affected patients.
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Extrahepatic Biliary Atresia

Hepatology, 1984
Extrahepatic biliary atresia is defined as partial or total absence of permeable bile duct between porta hepatis and the duodenum. The incidence varies from 1:8,000 to 1:10,000. Cholestasis is total and permanent. 131I Rose Bengal test and needle liver biopsy allow correct identification of 95% of cases before surgery Before ...
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Biliary Atresia

Pediatric Annals, 1985
R P, Altman, J, Levy
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Screening for biliary atresia

Pediatric Surgery International, 2017
Early diagnosis followed by proper KP is essential for the improvement of long-term prognosis for patients with BA. It is increasingly accepted that KP at ≤ 30 days of age significantly improves native liver survival rate. Published analyses in English and Japanese indicate that screening by SCC and DB/CB is potentially feasible. Screening with SCC has
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Biliary Atresia

The Guthrie Journal, 1955
D S, MOTSAY, A T, HALL
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Biliary Atresia

Journal of Pediatric Gastroenterology and Nutrition, 2002
Richard A, Schreiber, Ronald E, Kleinman
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Biliary Atresia

Clinics in Perinatology, 1978
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CD177+ cells produce neutrophil extracellular traps that promote biliary atresia

Journal of Hepatology, 2022
Zhe Wang, Huimin Xia, Yan Chen
exaly  

Biliary Atresia – emerging diagnostic and therapy opportunities

EBioMedicine, 2021
Urban Lendahl   +2 more
exaly  

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