Page last updated: 2024-11-08

serine and Cerebellar Ataxia

serine has been researched along with Cerebellar Ataxia in 2 studies

Serine: A non-essential amino acid occurring in natural form as the L-isomer. It is synthesized from GLYCINE or THREONINE. It is involved in the biosynthesis of PURINES; PYRIMIDINES; and other amino acids.
serine : An alpha-amino acid that is alanine substituted at position 3 by a hydroxy group.

Cerebellar Ataxia: Incoordination of voluntary movements that occur as a manifestation of CEREBELLAR DISEASES. Characteristic features include a tendency for limb movements to overshoot or undershoot a target (dysmetria), a tremor that occurs during attempted movements (intention TREMOR), impaired force and rhythm of diadochokinesis (rapidly alternating movements), and GAIT ATAXIA. (From Adams et al., Principles of Neurology, 6th ed, p90)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Ali, Z1
Zulfiqar, S1
Klar, J1
Wikström, J1
Ullah, F1
Khan, A1
Abdullah, U1
Baig, S1
Dahl, N1
Mišković, ND1
Domingo, A1
Dobričić, V1
Max, C1
Braenne, I1
Petrović, I1
Grütz, K1
Pawlack, H1
Tournev, I1
Kalaydjieva, L1
Svetel, M1
Lohmann, K1
Kostić, VS1
Westenberger, A1

Other Studies

2 other studies available for serine and Cerebellar Ataxia

ArticleYear
Homozygous GRID2 missense mutation predicts a shift in the D-serine binding domain of GluD2 in a case with generalized brain atrophy and unusual clinical features.
    BMC medical genetics, 2017, 12-06, Volume: 18, Issue:1

    Topics: Adult; Aged; Amino Acid Sequence; Atrophy; Base Sequence; Binding Sites; Brain; Cerebellar Ataxia; C

2017
Seemingly dominant inheritance of a recessive ANO10 mutation in romani families with cerebellar ataxia.
    Movement disorders : official journal of the Movement Disorder Society, 2016, Volume: 31, Issue:12

    Topics: Adult; Anoctamins; Cerebellar Ataxia; Electromyography; Family Health; Female; Humans; Male; Middle

2016