Compounds > threonine

threonine and Ataxia

threonine has been researched along with Ataxia in 5 studies

Research

Studies (5)

Timeframe	Studies, this research(%)	All Research%
pre-1990	1 (20.00)	18.7374
1990's	2 (40.00)	18.2507
2000's	1 (20.00)	29.6817
2010's	1 (20.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Berciano, J; Infante, J; Pelayo-Negro, AL; Rodríguez-Oroz, MC; Sánchez-Quintana, C; Tola-Arribas, MA; Volpini, V; Zeviani, M	1
Mantuano, E; Veneziano, L	1
Barbeau, A; Chouza, C; Roy, M	1
Bardet, J; Diry, C; Heron, B; Kamoun, P; Marsac, C; Munnich, A; Parvy, P; Ponsot, G; Rabier, D; Rotig, A; Rustin, P; Saudubray, JM	1
Goldin, AL; Smith, MR	1

Other Studies

5 other study(ies) available for threonine and Ataxia

Article	Year
Screening for POLG W748S and A467T mutations in ataxia patients from Spain. Movement disorders : official journal of the Movement Disorder Society, 2012, Sep-01, Volume: 27, Issue:10 Topics: Adult; Age of Onset; Aged; Alanine; Ataxia; DNA Polymerase gamma; DNA-Directed DNA Polymerase; Female; Gene Frequency; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Male; Middle Aged; Mutation; Polymorphism, Single Nucleotide; Serine; Spain; Threonine; Tryptophan; Young Adult	2012
Early onset progressive ataxia associated with the first CACNA1A mutation identified within the I-II loop. Journal of the neurological sciences, 2007, Dec-15, Volume: 263, Issue:1-2 Topics: Alanine; Ataxia; Calcium Channels; Disease Progression; Humans; Mutation; Protein Structure, Tertiary; Threonine	2007
Pilot study of threonine supplementation in human spasticity. The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques, 1982, Volume: 9, Issue:2 Topics: Adult; Ataxia; Double-Blind Method; Female; Humans; Male; Muscle Spasticity; Paralysis; Threonine	1982
Persistent hypocitrullinaemia as a marker for mtDNA NARP T 8993 G mutation? Journal of inherited metabolic disease, 1998, Volume: 21, Issue:3 Topics: Abnormalities, Multiple; Ataxia; Biomarkers; Child, Preschool; Citrulline; DNA, Mitochondrial; Female; Glycine; Humans; Infant; Male; Muscular Diseases; Mutation; Retinitis Pigmentosa; Threonine	1998
A mutation that causes ataxia shifts the voltage-dependence of the Scn8a sodium channel. Neuroreport, 1999, Sep-29, Volume: 10, Issue:14 Topics: Alanine; Amino Acid Substitution; Animals; Ataxia; Electrophysiology; Kinetics; Mice; Mutation; NAV1.6 Voltage-Gated Sodium Channel; Nerve Tissue Proteins; Oocytes; Reverse Transcriptase Polymerase Chain Reaction; Sodium Channels; Threonine; Xenopus	1999

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