dihydrolipoamide and thiamine

dihydrolipoamide has been researched along with thiamine in 1 studies

Research

Studies (1)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	0 (0.00)	29.6817
2010's	1 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Briones, P; Font, A; Pineda, M; Quintana, E; Ribes, A; Tort, F; Vilaseca, MA	1

Other Studies

1 other study(ies) available for dihydrolipoamide and thiamine

Article	Year
Dihydrolipoamide dehydrogenase (DLD) deficiency in a Spanish patient with myopathic presentation due to a new mutation in the interface domain. Journal of inherited metabolic disease, 2010, Volume: 33 Suppl 3 Topics: Acidosis, Lactic; Adult; Amino Acid Sequence; Base Sequence; Biomarkers; Blepharoptosis; Cells, Cultured; Dietary Supplements; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Heredity; Heterozygote; Homozygote; Humans; Lactic Acid; Maple Syrup Urine Disease; Molecular Sequence Data; Muscle Strength; Muscle Weakness; Mutation, Missense; Pedigree; Phenotype; Photophobia; Protein Structure, Tertiary; Pyruvate Dehydrogenase Complex Deficiency Disease; Spain; Thiamine; Thioctic Acid; Treatment Outcome	2010

Article

Year

Dihydrolipoamide dehydrogenase (DLD) deficiency in a Spanish patient with myopathic presentation due to a new mutation in the interface domain.

Journal of inherited metabolic disease, 2010, Volume: 33 Suppl 3

Topics: Acidosis, Lactic; Adult; Amino Acid Sequence; Base Sequence; Biomarkers; Blepharoptosis; Cells, Cultured; Dietary Supplements; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Heredity; Heterozygote; Homozygote; Humans; Lactic Acid; Maple Syrup Urine Disease; Molecular Sequence Data; Muscle Strength; Muscle Weakness; Mutation, Missense; Pedigree; Phenotype; Photophobia; Protein Structure, Tertiary; Pyruvate Dehydrogenase Complex Deficiency Disease; Spain; Thiamine; Thioctic Acid; Treatment Outcome

2010