Results 351 to 360 of about 917,291 (368)
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An intronic variation in SLC52A1 causes exon skipping and transient riboflavin-responsive multiple acyl-CoA dehydrogenation deficiency.

Molecular Genetics and Metabolism, 2017
S. Mosegaard   +9 more
semanticscholar   +1 more source

EXPERIMENTAL RIBOFLAVIN DEFICIENCY IN MAN

The American Journal of the Medical Sciences, 1943
John J. Boehrer   +2 more
openaire   +2 more sources

High rates of riboflavin deficiency in women of childbearing age in Cambodia and Canada (1041.12)

, 2014
Kyly C. Whitfield   +7 more
semanticscholar   +1 more source

Medical marijuana for cancer

Ca-A Cancer Journal for Clinicians, 2015
exaly  

Patient with multiple acyl-CoA dehydrogenation deficiency disease and FLAD1 mutations benefits from riboflavin therapy

Neuromuscular Disorders, 2017
M. Auranen   +10 more
semanticscholar   +1 more source

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