Page last updated: 2024-10-18

glycine and Adiadochokinesis

glycine has been researched along with Adiadochokinesis in 3 studies

Research Excerpts

ExcerptRelevanceReference
"Familial hemiplegic migraine type-1 (FHM-1) is caused by missense mutations in the CACNA1A gene that encodes the α1A pore-forming subunit of CaV2."1.42Familial hemiplegic migraine type-1 mutated cav2.1 calcium channels alter inhibitory and excitatory synaptic transmission in the lateral superior olive of mice. ( Di Guilmi, MN; Ferrari, MD; Forsythe, ID; Inchauspe, CG; Pilati, N; Uchitel, OD; Urbano, FJ; van den Maagdenberg, AM, 2015)

Research

Studies (3)

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

Authors

AuthorsStudies
Inchauspe, CG1
Pilati, N1
Di Guilmi, MN1
Urbano, FJ1
Ferrari, MD1
van den Maagdenberg, AM1
Forsythe, ID1
Uchitel, OD1
Grüsser-Cornehls, U1
Bäurle, J1
Nightingale, S1
Barton, ME1

Reviews

1 review available for glycine and Adiadochokinesis

ArticleYear
Mutant mice as a model for cerebellar ataxia.
    Progress in neurobiology, 2001, Volume: 63, Issue:5

    Topics: Animals; Ataxia; Cerebellar Ataxia; Cerebellum; Disease Models, Animal; gamma-Aminobutyric Acid; Gly

2001

Other Studies

2 other studies available for glycine and Adiadochokinesis

ArticleYear
Familial hemiplegic migraine type-1 mutated cav2.1 calcium channels alter inhibitory and excitatory synaptic transmission in the lateral superior olive of mice.
    Hearing research, 2015, Volume: 319

    Topics: Animals; Brain Stem; Calcium Channels, N-Type; Cerebellar Ataxia; Codon; Electrophysiology; Exons; G

2015
Intermittent vertical supranuclear ophthalmoplegia and ataxia.
    Movement disorders : official journal of the Movement Disorder Society, 1991, Volume: 6, Issue:1

    Topics: Cerebellar Ataxia; Child; Eye Movements; Female; Fever; Glycine; Humans; Ophthalmoplegia; Reflex, Ve

1991