leucine and Acidosis, Lactic

leucine has been researched along with Acidosis, Lactic in 3 studies

Research

Studies (3)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	2 (66.67)	18.2507
2000's	1 (33.33)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Deufel, T; Duran, M; Endres, W; Gibson, KM; Hadorn, HB; Ibel, H; Kennaway, NG; Paetzke, I	1
Koch, G; Mariman, E; Okhuijsen-Kroes, EJ; Sengers, RC; Smeitink, JA; Trijbels, JM; van den Heuvel, LP; Wendel, U	1
Fukushima, H; Inui, K; Midorikawa, M; Nishigaki, T; Okada, S; Tanaka, J; Taniike, M; Tsukamoto, H	1

Reviews

1 review(s) available for leucine and Acidosis, Lactic

Article	Year
Infantile presentation of the mtDNA A3243G tRNA(Leu (UUR)) mutation. Neuropediatrics, 2001, Volume: 32, Issue:4 Topics: Acidosis, Lactic; Child, Preschool; Diagnosis, Differential; DNA, Mitochondrial; Failure to Thrive; Fatal Outcome; Female; Humans; Infant; Infant, Newborn; Infant, Premature, Diseases; Leucine; Male; MELAS Syndrome; Mitochondrial Encephalomyopathies; Muscle Hypotonia; Muscle, Skeletal; Mutation; Phenotype	2001

Article

Year

Infantile presentation of the mtDNA A3243G tRNA(Leu (UUR)) mutation.

Neuropediatrics, 2001, Volume: 32, Issue:4

Topics: Acidosis, Lactic; Child, Preschool; Diagnosis, Differential; DNA, Mitochondrial; Failure to Thrive; Fatal Outcome; Female; Humans; Infant; Infant, Newborn; Infant, Premature, Diseases; Leucine; Male; MELAS Syndrome; Mitochondrial Encephalomyopathies; Muscle Hypotonia; Muscle, Skeletal; Mutation; Phenotype

2001

Other Studies

2 other study(ies) available for leucine and Acidosis, Lactic

Article	Year
Multiple respiratory chain abnormalities associated with hypertrophic cardiomyopathy and 3-methylglutaconic aciduria. European journal of pediatrics, 1993, Volume: 152, Issue:8 Topics: Acidosis, Lactic; Cardiomyopathy, Hypertrophic; Electron Transport Complex IV; Glutarates; Humans; Hydro-Lyases; Infant; Leucine; Male; Meglutol; Metabolism, Inborn Errors; Mitochondrial Myopathies; Respiration Disorders	1993
Mitochondrial encephalomyopathies with the mutation of the mitochondrial tRNA(Leu(UUR)) gene. The Journal of pediatrics, 1992, Volume: 120, Issue:1 Topics: Acidosis, Lactic; Adult; Blotting, Southern; Brain Diseases; Cerebrovascular Disorders; Child; Codon; DNA, Mitochondrial; Female; Humans; Leucine; Male; Mitochondria, Muscle; Muscular Diseases; Polymerase Chain Reaction; RNA; RNA, Mitochondrial; RNA, Transfer, Leu; Syndrome	1992

Article

Year

Multiple respiratory chain abnormalities associated with hypertrophic cardiomyopathy and 3-methylglutaconic aciduria.

European journal of pediatrics, 1993, Volume: 152, Issue:8

Topics: Acidosis, Lactic; Cardiomyopathy, Hypertrophic; Electron Transport Complex IV; Glutarates; Humans; Hydro-Lyases; Infant; Leucine; Male; Meglutol; Metabolism, Inborn Errors; Mitochondrial Myopathies; Respiration Disorders

1993

Mitochondrial encephalomyopathies with the mutation of the mitochondrial tRNA(Leu(UUR)) gene.

The Journal of pediatrics, 1992, Volume: 120, Issue:1

Topics: Acidosis, Lactic; Adult; Blotting, Southern; Brain Diseases; Cerebrovascular Disorders; Child; Codon; DNA, Mitochondrial; Female; Humans; Leucine; Male; Mitochondria, Muscle; Muscular Diseases; Polymerase Chain Reaction; RNA; RNA, Mitochondrial; RNA, Transfer, Leu; Syndrome

1992