Diagnosis and management of glycogen storage disease type IV, including adult polyglucosan body disease: A clinical practice resource-Reference-Cited by-同舟云学术

Diagnosis and management of glycogen storage disease type IV, including adult polyglucosan body disease: A clinical practice resource

Published:2023-03 Issue:3 Volume:138 Page:107525
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Koch Rebecca L.,Soler-Alfonso Claudia,Kiely Bridget T.,Asai Akihiro,Smith Ariana L.,Bali Deeksha S.,Kang Peter B.,Landstrom Andrew P.,Akman H. Orhan,Burrow T. Andrew,Orthmann-Murphy Jennifer L.,Goldman Deberah S.,Pendyal Surekha,El-Gharbawy Areeg H.,Austin Stephanie L.,Case Laura E.,Schiffmann Raphael,Hirano Michio,Kishnani Priya S.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference191 articles.

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5. Hyperphosphorylation of Glucosyl C6 carbons and altered structure of glycogen in the neurodegenerative epilepsy Lafora disease;Nitschke;Cell Metab.,2013

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3. Neuro-Ophthalmic Manifestations of Adult Polyglucosan Body Disease;Journal of Neuro-Ophthalmology;2024-08-15

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