Adult polyglucosan body disease: A case report of a manifesting heterozygote-Reference-Cited by-同舟云学术

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Adult polyglucosan body disease: A case report of a manifesting heterozygote

Published:2005 Issue:5 Volume:32 Page:675-681
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Ubogu Eroboghene E.,Hong Stacey Tay Kiat,Akman Hasan Orhan,Dimauro Salvatore,Katirji Bashar,Preston David C.,Shapiro Barbara E.

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Clinical Neurology,Physiology

Reference36 articles.

1. Muscle phosphofructokinase deficiency: Two cases with unusual polysaccharide accumulation and immunologically active enzyme protein

2. Corpora Amylacea of the Lumbar Spinal Cord and Peripheral Nervous System

3. Glycogen branching enzyme deficiency in adult polyglucosan body disease

4. Polyglucosan bodies in sural nerve biopsies

5. Adult polyglucosan body disease: The diagnostic value of axilla skin biopsy

Cited by 31 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A United States-based patient-reported adult polyglucosan body disease registry: initial results;Therapeutic Advances in Rare Disease;2024-01

2. Developmental and Inherited Liver Disease;MacSween's Pathology of the Liver;2024

3. Diagnosis and management of glycogen storage disease type IV, including adult polyglucosan body disease: A clinical practice resource;Molecular Genetics and Metabolism;2023-03

4. Characterization of cognitive impairment in adult polyglucosan body disease;Journal of Neurology;2022-01-08

5. Adult polyglucosan body disease: an acute presentation leading to unmasking of this rare disorder;Hospital Practice;2021-01-27

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