Developmental evolution in a patient with multiple acyl-coenzymeA dehydrogenase deficiency under pharmacological treatment-Reference-Cited by-同舟云学术

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Developmental evolution in a patient with multiple acyl-coenzymeA dehydrogenase deficiency under pharmacological treatment

Published:2012-03 Issue:2 Volume:16 Page:203-205
ISSN:1090-3798
Container-title:European Journal of Paediatric Neurology
language:en
Short-container-title:European Journal of Paediatric Neurology

Author:

Rosa M.,Pascarella A.,Parenti G.,Buono S.,Romano A.,Della Casa R.,Andria G.,Marino M.,Riccio M.P.,Bravaccio C.

Publisher

Elsevier BV

Subject

Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health

Reference6 articles.

1. Lipid storage Myopathy;Liang;Curr Neurol Neurosci Rep,2010

2. Multiple acyl-CoA dehydrogenase deficiency (MADD): a curable cause of genetic muscular lipidosis;Maillart;Rev Neurol,2010

3. Mechanisms underlying metabolic and neural defects in zebrafish and human multiple acyl-CoA dehydrogenase deficiency (MADD);Song;PLoS One,2009

4. Juvenile multiple sclerosis-like episodes associated with a defect of mithocondrial beta oxidation;Powell;Neurol,1990

5. Riboflavine-responsive defects of beta-oxidation;Gregersen;J Inherit Metab Dis,1985

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1. Successful pregnancy in a patient with multiple acyl-CoA dehydrogenase deficiency;Endocrinología, Diabetes y Nutrición (English ed.);2023-06

2. Case report: Novel ETFDH compound heterozygous mutations identified in a patient with late-onset glutaric aciduria type II;Frontiers in Neurology;2023-01-27

3. Successful pregnancy in a patient with multiple acyl-CoA dehydrogenase deficiency;Endocrinología, Diabetes y Nutrición;2022-06

4. Glutaric Acidemia, Pathogenesis and Nutritional Therapy;Frontiers in Nutrition;2021-12-15

5. Glutaric Aciduria Type II With Ketosis in a Male Infant;Cureus;2021-04-10

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