leucine and Decreased Muscle Tone

leucine has been researched along with Decreased Muscle Tone in 3 studies

Research

Studies (3)

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

Authors

Authors	Studies
Arné-Bes, MC; Delisle, MB; Figarella-Branger, D; Heitz, F; Levade, T; Pellissier, JF; Richard, P; Uro-Coste, E	1
Koch, G; Mariman, E; Okhuijsen-Kroes, EJ; Sengers, RC; Smeitink, JA; Trijbels, JM; van den Heuvel, LP; Wendel, U	1
Frasch, W; Junker, A; Lehnert, W; Niederhoff, H; Saule, H	1

Reviews

1 review(s) available for leucine and Decreased Muscle Tone

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 Decreased Muscle Tone

Article	Year
Striking phenotypic variability in two familial cases of myosin storage myopathy with a MYH7 Leu1793pro mutation. Neuromuscular disorders : NMD, 2009, Volume: 19, Issue:2 Topics: Amino Acid Substitution; Cardiac Myosins; Cardiomyopathies; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Genetic Variation; Genotype; Heart; Humans; Leucine; Middle Aged; Muscle Hypotonia; Muscle, Skeletal; Muscular Diseases; Mutation; Myocardium; Myosin Heavy Chains; Phenotype; Proline; Young Adult	2009
A case of biotin-responsive 3-methylcrotonylglycin- and 3-hydroxyisovaleric aciduria. European journal of pediatrics, 1979, Volume: 132, Issue:2 Topics: Amino Acid Metabolism, Inborn Errors; Biotin; Female; Humans; Infant; Leucine; Muscle Hypotonia; Seizures	1979

Article

Year

Striking phenotypic variability in two familial cases of myosin storage myopathy with a MYH7 Leu1793pro mutation.

Neuromuscular disorders : NMD, 2009, Volume: 19, Issue:2

Topics: Amino Acid Substitution; Cardiac Myosins; Cardiomyopathies; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Genetic Variation; Genotype; Heart; Humans; Leucine; Middle Aged; Muscle Hypotonia; Muscle, Skeletal; Muscular Diseases; Mutation; Myocardium; Myosin Heavy Chains; Phenotype; Proline; Young Adult

2009

A case of biotin-responsive 3-methylcrotonylglycin- and 3-hydroxyisovaleric aciduria.

European journal of pediatrics, 1979, Volume: 132, Issue:2

Topics: Amino Acid Metabolism, Inborn Errors; Biotin; Female; Humans; Infant; Leucine; Muscle Hypotonia; Seizures

1979