Riboflavin

Riboflavin-responsive glutaric aciduria type II presenting as a leukodystrophy

Magnetic Resonance Imaging / Treatment / Pediatric Neurology / Humans / Correlation / Male / Differential Diagnosis / Phenotype / Gas Chromatography/mass Spectrometry / Neurosciences / Brain Damage / Riboflavin / Nino / Magnetic resonance image / Male / Differential Diagnosis / Phenotype / Gas Chromatography/mass Spectrometry / Neurosciences / Brain Damage / Riboflavin / Nino / Magnetic resonance image

ANTIMALARIAL EFFECTS OF RIBOFLAVIN DEFICIENCY

Free Radicals / Malaria / Thalassemia / Adolescent / Humans / Child / Mice / Animals / Lancet / Pyridoxine / Rats / Oxygen / Erythrocytes / Flavins / Riboflavin / Child / Mice / Animals / Lancet / Pyridoxine / Rats / Oxygen / Erythrocytes / Flavins / Riboflavin

In vitro photochemical cataract in mice lacking copper-zinc superoxide dismutase

Photochemistry / Copper / Mice / Animals / Digital Image Analysis / Light / Cataract / Zinc / Superoxide Dismutase / Body water / Visible Light / Water Content / Enzymatic Activity / Superoxides / Riboflavin / Biochemistry and cell biology / Light / Cataract / Zinc / Superoxide Dismutase / Body water / Visible Light / Water Content / Enzymatic Activity / Superoxides / Riboflavin / Biochemistry and cell biology

Clinical, Biochemical, and Genetic Heterogeneity in Short-Chain Acyl-Coenzyme A Dehydrogenase Deficiency

Biochemistry / Genetics / Adolescent / Medicine / Genetic Diversity / Case Report / Humans / Child / Mutation / Female / Inborn errors of metabolism / Male / Statistical Significance / Infant / Netherlands / Newborn Screening / Phenotype / Newborn Infant / L-carnitine / Genotype / Deficiency / Retrospective Studies / Developmental delay / Autosomal Recessive / Deficit / Clinical Signs / Retrospective Study / Malonates / JAMA / Riboflavin / Case Report / Humans / Child / Mutation / Female / Inborn errors of metabolism / Male / Statistical Significance / Infant / Netherlands / Newborn Screening / Phenotype / Newborn Infant / L-carnitine / Genotype / Deficiency / Retrospective Studies / Developmental delay / Autosomal Recessive / Deficit / Clinical Signs / Retrospective Study / Malonates / JAMA / Riboflavin

Nutrition support for glutaric acidemia type I

Mitochondria / Humans / Child / Female / Male / Oxidoreductases / Infant / Tryptophan / Newborn Infant / L-carnitine / Lysine / Riboflavin / Child preschool / Oxidoreductases / Infant / Tryptophan / Newborn Infant / L-carnitine / Lysine / Riboflavin / Child preschool

Nutrition support for glutaric acidemia type I

Mitochondria / Humans / Child / Female / Male / Oxidoreductases / Infant / Tryptophan / Newborn Infant / L-carnitine / Lysine / Riboflavin / Child preschool / Oxidoreductases / Infant / Tryptophan / Newborn Infant / L-carnitine / Lysine / Riboflavin / Child preschool
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