Exokrine Pankreasinsuffizienz bei Morbus Wilson

Author:

O�wald P.,Niessen K. H.

Publisher

Springer Science and Business Media LLC

Subject

General Medicine,Genetics (clinical),Drug Discovery,Molecular Medicine

Reference16 articles.

1. Bearn, A.G.: Wilson's Disease in the Metabolic Basic of Inherited Diseases. Edit. J.B. Stanbury, J.B. Wyngaarden and D.I. Frederickson. Frederickson. Third Edition, McGraw Hill New York 1972 S. 1033

2. Benson, G.D.: Chronic active liver disease with excessive hepatic copper storage. Gastroenterology64, 153 (1973)

3. Davenport, H.W.: Physiologie der Verdauung. Schattauer Verlag Stuttgart-New York 1971 S. 259

4. Frommer, D.J.: Defective biliary excretion of copper in Wilson's disease. Gut15, 125?129 (1974)

5. Goedde, H.W., Benkemann, H.G., Lange, J., Harders, H.: Quantitative Bestimmung und Phänotypisierung des Cäruloplasmins bei Morbus Wilson. Klin. Wschr.53, 731?734 (1975)

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1. Recurrent acute pancreatitis in a Wilson disease patient: an unusual association;Egyptian Liver Journal;2021-08-18

2. Sekundäre, tumorartige, zystische und transplantationsbedingte Pankreasveränderungen;Pathologie;2020

3. Copper Metabolism and Wilson’s Disease;Modern Concepts in Gastroenterology Volume 3;1992

4. Reply;Gastroenterology;1989-05

5. Wilsonʼs Disease Associated with Pancreatitis;Journal of Pediatric Gastroenterology and Nutrition;1988-11

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