Results 291 to 300 of about 944,643 (357)
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Food & Function, 2020
SCOPE Epidemiologic evidence suggests that riboflavin (RBF) deficiency is a specific nutritional predisposition for esophageal cancer. The aim of this study is to investigate the potential roles of gut microbiota in esophageal tumorigenesis caused by the
Feng Pan +9 more
semanticscholar +1 more source
SCOPE Epidemiologic evidence suggests that riboflavin (RBF) deficiency is a specific nutritional predisposition for esophageal cancer. The aim of this study is to investigate the potential roles of gut microbiota in esophageal tumorigenesis caused by the
Feng Pan +9 more
semanticscholar +1 more source
Cataracts and riboflavin deficiency
The American Journal of Clinical Nutrition, 1981Lenticular reduced glutathione, diminished in all forms fo human cataract, requires flavin adenine dinucleotide as a coenzyme for glutathione reductase. Deficiency of riboflavin, a precursor of flavin adenine dinucleotide, has been believed by some to be associated with cataract formation. We evaluated the riboflavin nutritional status of healthy young
H W, Skalka, J T, Prchal
openaire +2 more sources
Food & Function, 2019
Fish is among the cheapest and most promising sources of animal protein. The main edible portion of fish is muscle. This study explored the impact of dietary riboflavin on fish flesh quality and showed the possible role of muscle antioxidant defense in ...
Wei‐dan Jiang +9 more
semanticscholar +1 more source
Fish is among the cheapest and most promising sources of animal protein. The main edible portion of fish is muscle. This study explored the impact of dietary riboflavin on fish flesh quality and showed the possible role of muscle antioxidant defense in ...
Wei‐dan Jiang +9 more
semanticscholar +1 more source
ANTIMALARIAL EFFECTS OF RIBOFLAVIN DEFICIENCY
The Lancet, 1985La carence en riboflavine modifie l'activite de plusieurs enzymes du metabolisme intermediaire, ce qui a pour effet une protection vis-a-vis du paludisme. L'addition de riboflavine aux milieux de culture inhibe l'activite in vitro de plusieurs medicaments sur P. falciparum.
P, Dutta, J, Pinto, R, Rivlin
openaire +4 more sources
American Journal of Medical Genetics. Part A, 2020
Riboflavin transporter deficiency (RTD) (MIM #614707) is a neurogenetic disorder with its most common manifestations including sensorineural hearing loss, peripheral neuropathy, respiratory insufficiency, and bulbar palsy.
Nishitha R. Pillai +9 more
semanticscholar +1 more source
Riboflavin transporter deficiency (RTD) (MIM #614707) is a neurogenetic disorder with its most common manifestations including sensorineural hearing loss, peripheral neuropathy, respiratory insufficiency, and bulbar palsy.
Nishitha R. Pillai +9 more
semanticscholar +1 more source
Journal of Neurology Neurosurgery & Psychiatry, 2020
Objective Riboflavin transporter deficiencies (RTDs), involving SLC52A3 and SLC52A2 genes, have recently been related to Brown-Vialetto-Van Laere (BVVL) syndrome, a hereditary paediatric condition associating motor neuropathy (MN) and deafness.
C. Carreau +10 more
semanticscholar +1 more source
Objective Riboflavin transporter deficiencies (RTDs), involving SLC52A3 and SLC52A2 genes, have recently been related to Brown-Vialetto-Van Laere (BVVL) syndrome, a hereditary paediatric condition associating motor neuropathy (MN) and deafness.
C. Carreau +10 more
semanticscholar +1 more source
Strachan’s syndrome and riboflavin deficiency
Practical NeurologyStrachan’s syndrome comprises a triad of optic, auditory and painful sensory peripheral neuropathy. It has been recognised since the late 19th century and is presumed to result from nutritional deficiency. Patients present acute or subacutely after a period of systemic illness, weight loss or, most commonly, dietary restriction, especially veganism ...
Caroline Kramarz +2 more
openaire +2 more sources
Annals of Neurology, 2018
Riboflavin‐responsive multiple acyl–coenzyme A dehydrogenation deficiency (RR‐MADD) is an inherited fatty acid metabolism disorder mainly caused by genetic defects in electron transfer flavoprotein–ubiquinone oxidoreductase (ETF:QO).
Jingwen Xu +14 more
semanticscholar +1 more source
Riboflavin‐responsive multiple acyl–coenzyme A dehydrogenation deficiency (RR‐MADD) is an inherited fatty acid metabolism disorder mainly caused by genetic defects in electron transfer flavoprotein–ubiquinone oxidoreductase (ETF:QO).
Jingwen Xu +14 more
semanticscholar +1 more source