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alanine and Basal Ganglia Diseases

alanine has been researched along with Basal Ganglia Diseases in 3 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.

Basal Ganglia Diseases: Diseases of the BASAL GANGLIA including the PUTAMEN; GLOBUS PALLIDUS; claustrum; AMYGDALA; and CAUDATE NUCLEUS. DYSKINESIAS (most notably involuntary movements and alterations of the rate of movement) represent the primary clinical manifestations of these disorders. Common etiologies include CEREBROVASCULAR DISORDERS; NEURODEGENERATIVE DISEASES; and CRANIOCEREBRAL TRAUMA.

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (33.33)29.6817
2010's2 (66.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Serrano, M1
Rebollo, M1
Depienne, C1
Rastetter, A1
Fernández-Álvarez, E1
Muchart, J1
Martorell, L1
Artuch, R1
Obeso, JA1
Pérez-Dueñas, B1
Ohnuma, T1
Sakai, Y1
Maeshima, H1
Higa, M1
Hanzawa, R1
Kitazawa, M1
Hotta, Y1
Katsuta, N1
Takebayashi, Y1
Shibata, N1
Arai, H1
Morava, E1
Rodenburg, RJ1
Hol, F1
de Vries, M1
Janssen, A1
van den Heuvel, L1
Nijtmans, L1
Smeitink, J1

Other Studies

3 other studies available for alanine and Basal Ganglia Diseases

ArticleYear
Reversible generalized dystonia and encephalopathy from thiamine transporter 2 deficiency.
    Movement disorders : official journal of the Movement Disorder Society, 2012, Sep-01, Volume: 27, Issue:10

    Topics: Adolescent; Alanine; Basal Ganglia; Basal Ganglia Diseases; Child, Preschool; Choline; Dystonic Diso

2012
No correlation between plasma NMDA-related glutamatergic amino acid levels and cognitive function in medicated patients with schizophrenia.
    International journal of psychiatry in medicine, 2012, Volume: 44, Issue:1

    Topics: Adolescent; Adult; Aged; Alanine; Antipsychotic Agents; Basal Ganglia Diseases; Biomarkers; Brief Ps

2012
Clinical and biochemical characteristics in patients with a high mutant load of the mitochondrial T8993G/C mutations.
    American journal of medical genetics. Part A, 2006, Apr-15, Volume: 140, Issue:8

    Topics: Adenosine Triphosphate; Alanine; Basal Ganglia Diseases; Child; Child, Preschool; DNA, Mitochondrial

2006