Die intrahepatische, familiäre Cholestase – Manifestation bei einer Jugendlichen mit Pruritus und Ikterus nach Beginn oraler Kontrazeption
Author:
Publisher
Springer Science and Business Media LLC
Subject
Surgery,Pediatrics, Perinatology and Child Health
Link
https://link.springer.com/content/pdf/10.1007/s00112-023-01806-7.pdf
Reference17 articles.
1. Summerskill WH, Walshe JM (1959) Benign recurrent intrahepatic “obstructive” jaundice. Lancet 2:686–690. https://doi.org/10.1016/S0140-6736(59)92128-2
2. Tygstrup N, Jensen B (1969) Intermittent intrahepatic cholestasis of unknown etiology in five young males from the Faroe Islands. Acta Med Scand 185:523–530. https://doi.org/10.1111/J.0954-6820.1969.TB07378.X
3. Bull LN, van Eijk MJ, Pawlikowska L et al (1998) A gene encoding a P-type ATPase mutated in two forms of hereditary cholestasis. Nat Genet 18:219–224. https://doi.org/10.1038/NG0398-219
4. Bull LN, Carlton VE, Stricker NL et al (1997) Genetic and morphological findings in progressive familial intrahepatic cholestasis (Byler disease PFIC‑1 and Byler syndrome): evidence for heterogeneity. Hepatology 26:155–164. https://doi.org/10.1002/HEP.510260121
5. Trauner M, Meier PJ, Boyer JL (1998) Molecular pathogenesis of cholestasis. N Engl J Med 339:1217–1227. https://doi.org/10.1056/nejm199810223391707
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