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Mitochondrial myopathy simulating spinal muscular atrophy

Published:1996-09 Issue:2 Volume:15 Page:153-158
ISSN:0887-8994
Container-title:Pediatric Neurology
language:en
Short-container-title:Pediatric Neurology

Author:

Pons Roser,Andreetta Francesca,Wang Ching H.,Vu Tuan H.,Bonilla Eduardo,DiMauro Salvatore,De Vivo Darryl C.

Publisher

Elsevier BV

Subject

Clinical Neurology,Developmental Neuroscience,Neurology,Pediatrics, Perinatology, and Child Health

Reference20 articles.

1. Motor neuron diseases in children;Gomez,1994

2. Genetic mapping of chronic childhood-onset spinal muscular atrophy to chromosome 5q11.2-13.3;Brzustowicz;Nature,1990

3. Genetic homogeneity between acute and chronic forms of spinal muscular atrophy;Gilliam;Nature,1990

4. Gene for chronic proximal spinal muscular atrophies maps to chromosome 5q;Melki;Nature,1990

5. Phenotypic heterogeneity of spinal muscular atrophy mapping to chromosome 5q11.2-13.3 (SMA5q);Munsat;Neurology,1990

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1. Mitochondrial Dysfunction in Spinal Muscular Atrophy;International Journal of Molecular Sciences;2022-09-17

2. Mitochondrial stress responses in Duchenne muscular dystrophy: metabolic dysfunction or adaptive reprogramming?;American Journal of Physiology-Cell Physiology;2022-09-01

3. Advances in Thymidine Kinase 2 Deficiency: Clinical Aspects, Translational Progress, and Emerging Therapies;Journal of Neuromuscular Diseases;2022-03-01

4. Revisiting the role of mitochondria in spinal muscular atrophy;Cellular and Molecular Life Sciences;2021-04-05

5. Mtochonrial Neurology: A Tale of Two Genomes;Mitochondrial Diseases;2021

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