Muscle carnitine deficiency and lipid storage myopathy in patients with mitochondrial myopathy-Reference-Cited by-同舟云学术

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Muscle carnitine deficiency and lipid storage myopathy in patients with mitochondrial myopathy

Published:1993-07 Issue:7 Volume:16 Page:778-781
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Campos Yolanda,Huertas Rosa,Bautista Juan,Gutierrez Eduardo,Aparicio Manuel,Lorenzo Gustavo,Segura Dolores,Villanueva Mercedes,Cabello Ana,Alesso Luis,Arenas Joaquin

Publisher

Wiley

Subject

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

Reference18 articles.

1. CARNITINE

2. Plasma carnitine insufficiency and effectiveness ofL-carnitine therapy in patients with mitochondril myopathy

3. Book review

4. Systemic carnitine deficiency due to lack of electron transfer flavoprotein: ubiquinone oxidoreductase

5. Propionylcarnitine excretion in propionic and methylmalonic acidurias: a cause of carnitine deficiency

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1. Clinical Reasoning: A 60-Year-Old Woman With Rapidly Progressive Muscle Weakness and Ophthalmoparesis;Neurology;2024-08-13

2. Treatment Possibilities of Muscle Cramps in Patients with Liver Cirrhosis;Internal Medicine;2021-12-01

3. Efficacy of L-carnitine on ribavirin-induced hemolytic anemia in patients with hepatitis C virus infection;Clinical and Molecular Hepatology;2019-03-25

4. Monitoring clinical progression with mitochondrial disease biomarkers;Brain;2017-08-03

5. Metabolic Myopathies;Seminars in Neurology;2015-10-06

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