Acute axonal neuropathy in maple syrup urine disease-Reference-Cited by-同舟云学术

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Acute axonal neuropathy in maple syrup urine disease

Published:2001 Issue:2 Volume:24 Page:284-287
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Kleopa Kleopas A.,Raizen David M.,Friedrich Christopher A.,Brown Mark J.,Bird Shawn J.

Publisher

Wiley

Subject

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

Reference18 articles.

1. Maple syrup urine disease: It has come a long way

2. Disorders of branched chain amino acid and keto acid metabolism. In: editors. The metabolic and molecular bases of inherited disease. New York: McGraw-Hill; 1995. p 1239-1277.

3. Metabolism of the white blood cells in maple-syrup-urine disease

4. Further Observations on the Biochemical Lesion in Maple Syrup Urine Disease

5. AN ACUTE AXONAL FORM OF GUILLAIN-BARRÉE POLYNEUROPATHY

Cited by 8 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. Branched-Chain Organic Acidurias/Acidaemias;Inborn Metabolic Diseases;2022

2. Brain Branched-Chain Amino Acids in Maple Syrup Urine Disease: Implications for Neurological Disorders;International Journal of Molecular Sciences;2020-10-11

3. Peripheral neuropathy in complex inherited diseases: an approach to diagnosis;Journal of Neurology, Neurosurgery & Psychiatry;2017-08-09

4. Branched-chain Organic Acidurias/Acidaemias;Inborn Metabolic Diseases;2016

5. Ahornsirupkrankheit (MSUD);Angeborene Stoffwechselkrankheiten bei Erwachsenen;2014

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