Compounds > lysine
Page last updated: 2024-08-17

lysine and Cerebellar Ataxia

lysine has been researched along with Cerebellar Ataxia in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19901 (20.00)18.7374
1990's1 (20.00)18.2507
2000's0 (0.00)29.6817
2010's2 (40.00)24.3611
2020's1 (20.00)2.80

Authors

AuthorsStudies
Bernardini, JP; Cobbold, SA; Cotton, TR; Lechtenberg, BC; Richardson, LW; Wang, XS1
Cai, X; Long, L; Lu, Z; Shu, Y1
Barcs, G; Finta, L; Holló, A; Kamondi, A; Osztie, E; Papp, E; Sólyom, A; Szucs, A; Várallyay, P; Varga, D1
Terada, N1
Frey, HJ; Frey, ML; Riekkinen, PJ; Tuomola, HO1

Reviews

1 review(s) available for lysine and Cerebellar Ataxia

ArticleYear
[L-2-hydroxyglutaric aciduria].
    Ryoikibetsu shokogun shirizu, 1998, Issue:18 Pt 1

    Topics: Amino Acid Metabolism, Inborn Errors; Brain; Cerebellar Ataxia; Diagnosis, Differential; Glutarates; Humans; Lysine; Magnetic Resonance Imaging; Prognosis; Psychomotor Disorders

1998

Other Studies

4 other study(ies) available for lysine and Cerebellar Ataxia

ArticleYear
Structural basis of K63-ubiquitin chain formation by the Gordon-Holmes syndrome RBR E3 ubiquitin ligase RNF216.
    Molecular cell, 2022, 02-03, Volume: 82, Issue:3

    Topics: Allosteric Regulation; Binding Sites; Catalysis; Cerebellar Ataxia; Crystallography, X-Ray; Genetic Predisposition to Disease; Gonadotropin-Releasing Hormone; HEK293 Cells; Humans; Hypogonadism; Loss of Function Mutation; Lysine; Models, Molecular; Phenotype; Phosphorylation; Protein Binding; Protein Conformation; Protein Processing, Post-Translational; Structure-Activity Relationship; Ubiquitin-Protein Ligases; Ubiquitination

2022
A family with hereditary cerebellar ataxia finally confirmed as Gerstmann-Straussler-Scheinker syndrome with P102L mutation in PRNP gene.
    Neurosciences (Riyadh, Saudi Arabia), 2017, Volume: 22, Issue:2

    Topics: Cerebellar Ataxia; Family Health; Female; Gerstmann-Straussler-Scheinker Disease; Humans; Lysine; Magnetic Resonance Imaging; Middle Aged; Mutation; Prion Proteins; Proline

2017
Clinical experiences with Creutzfeldt-Jakob disease: three case studies.
    Ideggyogyaszati szemle, 2012, Nov-30, Volume: 65, Issue:11-12

    Topics: Aged; Autopsy; Brain; Cerebellar Ataxia; Creutzfeldt-Jakob Syndrome; Diagnosis, Differential; Electroencephalography; Fatal Outcome; Female; Glutamic Acid; Humans; Lysine; Magnetic Resonance Imaging; Male; Middle Aged; Mutation; Prion Proteins; Prions; Seizures; Speech Disorders

2012
A family with autosomal dominant spinocerebellar ataxia, with electrophysiological findings.
    Annals of clinical research, 1973, Volume: 5, Issue:3

    Topics: Action Potentials; Adult; Aged; Ataxia; Beta-Globulins; Cerebellar Ataxia; Electromyography; Female; Foot Deformities, Congenital; Histidine; Humans; Lysine; Male; Methods; Middle Aged; Neural Conduction; Nystagmus, Pathologic; Optic Atrophy; Pedigree

1973