Results 171 to 177 of about 470,683 (177)
Some of the next articles are maybe not open access.

NADH-CoQ REDUCTASE DEFICIENT MYOPATHY: SUCCESSFUL TREATMENT WITH RIBOFLAVIN

The Lancet, 1983
W.F.M. Arts   +4 more
openaire   +1 more source

95 A mouse model of Parkinson’s Disease based on CoQ deficiency

Mitochondrion, 2010
David L. Gasser   +4 more
openaire   +1 more source

CoQ10 Supplementation Rescues Nephrotic Syndrome Through Normalization of H2S Oxidation Pathway

Biochimica Et Biophysica Acta - Molecular Basis of Disease, 2018
Yimeng Xu   +2 more
exaly  

Dysfunctional Coq9 Protein Causes Predominant Encephalomyopathy Associated With CoQ Deficiency.

Human Molecular Genetics, 2013
Laura García-Corzo   +2 more
exaly  

4-Hydroxybenzoate supplementation in primary CoQ deficiency due to COQ2 defects

Introduction: Coenzyme Q (CoQ) is lipophilic, redox-active lipid involved in multiple cellular pathways. Its main role is to transport electrons from complex I and II to complex III of the mitochondrial respiratory chain. Primary CoQ deficiency is a rare mitochondrial disorder caused by mutations in genes involved in CoQ10 biosynthesis.
openaire   +1 more source

COQ 10 deficiency in statin related Myopathy.

2005
C. Lamperti   +10 more
openaire   +1 more source

Deficiency of coenzyme Q 10 in a succinate-CoQ 10 -Enzyme in the dystrophic rabbit on an antioxidant deficient diet.

International journal for vitamin and nutrition research. Internationale Zeitschrift fur Vitamin- und Ernahrungsforschung. Journal international de vitaminologie et de nutrition, 1972
G P, Littarru   +3 more
openaire   +1 more source

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