threonine has been researched along with Motor Neuron Disease in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (25.00) | 18.2507 |
2000's | 3 (75.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Leigh, PN; Mitsumoto, H; Parton, M | 2 |
Al-Lozi, MT; Baker, M; Baloh, RH; Bigio, EH; Cairns, NJ; Caselli, R; Chakraverty, S; Gitcho, MA; Goate, AM; Hatanpaa, KJ; Levitch, D; Mayo, K; Morris, JC; Norton, JB; Pestronk, A; Rademakers, R; White, CL | 1 |
Haque, A; Khan, JK; Kuo, YH; Lambein, F | 1 |
2 review(s) available for threonine and Motor Neuron Disease
Article | Year |
---|---|
Amino acids for amyotrophic lateral sclerosis / motor neuron disease.
Topics: Amino Acids, Branched-Chain; Amyotrophic Lateral Sclerosis; Humans; Motor Neuron Disease; Randomized Controlled Trials as Topic; Threonine | 2003 |
WITHDRAWN: Amino acids for amyotrophic lateral sclerosis / motor neuron disease.
Topics: Amino Acids, Branched-Chain; Amyotrophic Lateral Sclerosis; Humans; Motor Neuron Disease; Randomized Controlled Trials as Topic; Threonine | 2008 |
2 other study(ies) available for threonine and Motor Neuron Disease
Article | Year |
---|---|
TDP-43 A315T mutation in familial motor neuron disease.
Topics: Aged; Aged, 80 and over; Alanine; Amino Acid Sequence; Amino Acid Substitution; DNA Mutational Analysis; DNA-Binding Proteins; Female; Genes, Dominant; Humans; Male; Middle Aged; Molecular Sequence Data; Motor Neuron Disease; Mutation, Missense; Pedigree; Threonine | 2008 |
Inhibitory and excitatory amino acids in cerebrospinal fluid of neurolathyrism patients, a highly prevalent motorneurone disease.
Topics: Adolescent; Adult; Aged; Alanine; Aspartic Acid; Eating; Excitatory Amino Acids; Fabaceae; Glutamic Acid; Glycine; Humans; Isoleucine; Middle Aged; Motor Neuron Disease; Neurotoxins; Plants, Medicinal; Taurine; Threonine | 1995 |