Lipid Storage Myopathy due to Glutaric Aciduria Type II: Treatment of a Potentially Fatal Myopathy-Reference-Cited by-同舟云学术

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Lipid Storage Myopathy due to Glutaric Aciduria Type II: Treatment of a Potentially Fatal Myopathy

Published:2008-11-12 Issue:5 Volume:30 Page:667-672
ISSN:0012-1622
Container-title:Developmental Medicine & Child Neurology
language:en
Short-container-title:

Author:

Turnbull D. M.,Bartlett K.,Eyre J. A.,Gardner-Medwin D.,Johnson M. A.,Fisher J.,Watmough N. J.

Publisher

Wiley

Subject

Neurology (clinical),Developmental Neuroscience,Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-8749.1988.tb04806.x/fullpdf

Reference31 articles.

1. Multiple acyl-CoA dehydrogenation deficiency (glutaric aciduria type II), congenital polycystic kidneys, and symmetric warty dysplasia of the cerebral cortex in two newborn brothers. II: Morthology and pathogenesis;Böhm;European Journal of Pediatrics,1982

2. Muscle fibre types: how many and what kind;Brooke;Archives of Neurology,1970

3. A method for the determination of carnitine in the picomole range;Cederblad;Cinica Chimica Acta,1972

4. Fatal cases of lipid storage myopathy with carnitine deficiency;Cornelio;Journal of Neurology, Neurosurgery and Psychiatry,1977

5. Neonatal glutaric aciduria type II: an X-linked recessive inherited disorder;Coude;Human Genetics,1981

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1. Successful Pregnancy in a Young Woman with Multiple Acyl-CoA Dehydrogenase Deficiency;JIMD Reports;2017

2. Glutaric aciduria type 2 presenting with acute respiratory failure in an adult;Respiratory Medicine Case Reports;2015

3. Mitochondrial Reactive Oxygen Species (ROS) and ROS-Induced ROS Release;Physiological Reviews;2014-07

4. The electron transfer flavoprotein: Ubiquinone oxidoreductases;Biochimica et Biophysica Acta (BBA) - Bioenergetics;2010-12

5. Glutaric Aciduria Type 2, Late Onset Type in Thai Siblings With Myopathy;Pediatric Neurology;2010-10

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