Two cases of a non-progressive hepatic form of glycogen storage disease type IV with atypical liver pathology-Reference-Cited by-同舟云学术

Two cases of a non-progressive hepatic form of glycogen storage disease type IV with atypical liver pathology

Published:2020-09 Issue: Volume:24 Page:100601
ISSN:2214-4269
Container-title:Molecular Genetics and Metabolism Reports
language:en
Short-container-title:Molecular Genetics and Metabolism Reports

Author:

Ichimoto Keiko,Fujisawa Tomoo,Shimura Masaru,Fushimi Takuya,Tajika Makiko,Matsunaga Ayako,Ogawa-Tominaga Minako,Akiyama Nana,Naruke Yuki,Horie Hiroshi,Fukuda Tokiko,Sugie Hideo,Inui Ayano,Murayama Kei

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology

Reference16 articles.

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2. A new variant of type IV glycogenosis: deficiency of branching enzyme activity without apparent progressive liver disease;Greene;Hepatology,1988

3. Clinical and genetic heterogeneity of branching enzyme deficiency (glycogenosis type IV);Bruno;Neurology.,2004

4. Neuropathological study of skeletal muscle, heart, liver, and brain in a neonatal form of glycogen storage disease type IV associated with a new mutation in GBE1 gene;Lamperti;J. Inherit. Metab. Dis.,2009

5. Lafora disease;Turnbull;Epileptic Disord.,2016

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4. The potential of dietary treatment in patients with glycogen storage disease type IV;Journal of Inherited Metabolic Disease;2020-12-21