Page last updated: 2024-11-08

alanine and Chorea

alanine has been researched along with Chorea in 4 studies

Alanine: A non-essential amino acid that occurs in high levels in its free state in plasma. It is produced from pyruvate by transamination. It is involved in sugar and acid metabolism, increases IMMUNITY, and provides energy for muscle tissue, BRAIN, and the CENTRAL NERVOUS SYSTEM.
alanine : An alpha-amino acid that consists of propionic acid bearing an amino substituent at position 2.

Chorea: Involuntary, forcible, rapid, jerky movements that may be subtle or become confluent, markedly altering normal patterns of movement. Hypotonia and pendular reflexes are often associated. Conditions which feature recurrent or persistent episodes of chorea as a primary manifestation of disease are referred to as CHOREATIC DISORDERS. Chorea is also a frequent manifestation of BASAL GANGLIA DISEASES.

Research

Studies (4)

TimeframeStudies, this research(%)All Research%
pre-19901 (25.00)18.7374
1990's0 (0.00)18.2507
2000's3 (75.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
COWIE, V1
SEAKINS, JW1
Chen, DH1
Matsushita, M1
Rainier, S1
Meaney, B1
Tisch, L1
Feleke, A1
Wolff, J1
Lipe, H1
Fink, J1
Bird, TD1
Raskind, WH1
Stefanova, E1
Djarmati, A1
Momcilović, D1
Dragasević, N1
Svetel, M1
Klein, C1
Kostić, VS1
Wiltshire, EJ1
Poplawski, NK1
Harbord, MG1
Harrison, RJ1
Fletcher, JM1

Other Studies

4 other studies available for alanine and Chorea

ArticleYear
Urinary alanine excretor in a Huntington's chorea family.
    The Journal of mental science, 1962, Volume: 108

    Topics: Alanine; Body Fluids; Chorea; Humans; Huntington Disease

1962
Presence of alanine-to-valine substitutions in myofibrillogenesis regulator 1 in paroxysmal nonkinesigenic dyskinesia: confirmation in 2 kindreds.
    Archives of neurology, 2005, Volume: 62, Issue:4

    Topics: Alanine; Amino Acid Substitution; Chorea; Chromosome Mapping; Chromosomes, Human, Pair 2; DNA Mutati

2005
Clinical characteristics of paroxysmal nonkinesigenic dyskinesia in Serbian family with Myofibrillogenesis regulator 1 gene mutation.
    Movement disorders : official journal of the Movement Disorder Society, 2006, Volume: 21, Issue:11

    Topics: Adolescent; Adult; Alanine; Chorea; DNA Mutational Analysis; Family Health; Female; Humans; Male; Mi

2006
Ornithine carbamoyltransferase deficiency presenting with chorea in a female.
    Journal of inherited metabolic disease, 2000, Volume: 23, Issue:8

    Topics: Alanine; Chorea; Female; Glutamine; Humans; Infant; Ornithine Carbamoyltransferase Deficiency Diseas

2000