Sprue, Morbus Wilson und hereditäre Speichererkrankungen
Author:
Publisher
Springer Berlin Heidelberg
Link
https://link.springer.com/content/pdf/10.1007/978-3-662-62484-5_31
Reference27 articles.
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3. Burton BK, Deegan PB, Enns GM, Guardamagna O, Horslen S, Hovingh GK, Lobritto SJ, Malinova V, McLin VA, Raiman J, Di Rocco M, Santra S, Sharma R, Sykut-Cegielska J, Whitley CB, Eckert S, Valayannopoulos V, and Quinn AG (2015a). Clinical Features of Lysosomal Acid Lipase Deficiency – a Longitudinal Assessment of 48 Children and Adults. J Pediatr Gastroenterol Nutr.
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5. Canbay A, Müller MN, Philippou S, Gerken G, Tromm A (2018) Cholesteryl ester storage disease: fatal outcome without causal therapy in a female patient with the preventable sequelae of progressive liver disease after many years of mild symptoms. Am J Case Rep 19:577–581
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