Type III glycogenosis presenting as liver disease in adults with atypical histological features.-Reference-Cited by-同舟云学术

Type III glycogenosis presenting as liver disease in adults with atypical histological features.

Published:1983-04-01 Issue:4 Volume:36 Page:431-434
ISSN:0021-9746
Container-title:Journal of Clinical Pathology
language:en
Short-container-title:Journal of Clinical Pathology

Author:

Fellows I W,Lowe J S,Ogilvie A L,Stevens A,Toghill P J,Atkinson M

Publisher

BMJ

Subject

General Medicine,Pathology and Forensic Medicine

Reference9 articles.

1. Overeen bijondere stoornis in de koothydratenstofliseling in de kinderleeftijd;S, Van Creveld;Mandschr Neder Geneeskunds

2. Glycogen storage diseases;Hug, G.;Birth Defects,1976

3. The glycogenoses and other inherited disorders of carbohydrate metabolism;Senior, B.; Sedeghi-Nejad, A.;Clin Perinatol,1976

4. Glycogen storage diseases types I to X: criteria for morphological diagnosis;McAdalns, A.J.; Hug, G.; Bove, K.E.;Hum Pathol,1974

5. Glycogen storage disease in Israel. A clinical, biochemical and genetic study;Levin, S.; Moses, S.W.; Chayoth, R.; Jogoda, N.; Steinitz, K.;IsrJ Med Sci,1967

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