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

lysine and Cerebellar Diseases

lysine has been researched along with Cerebellar Diseases in 3 studies

Research

Studies (3)

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

Authors

AuthorsStudies
Dillmann, U; Erdmann, P; Papanagiotou, P; Shamdeen, MG; Sühs, KW1
Ferrer, I; García-Segura, JM; Pascual-Castroviejo, I; Pascual-Pascual, SI; Ugarte, M; Velázquez Fragua, R1
Appleton, D; Coman, D; Jaeken, J; Klingberg, S; MacDonald, R; McGill, J; Morris, D1

Other Studies

3 other study(ies) available for lysine and Cerebellar Diseases

ArticleYear
Adult manifestation of L-2-hydroxyglutarate dehydrogenase deficiency by a novel mutation.
    Neurology, 2012, Apr-10, Volume: 78, Issue:15

    Topics: Adult; Alcohol Oxidoreductases; Brain; Cerebellar Diseases; Cognition Disorders; Disease Progression; Female; Humans; Lysine; Magnetic Resonance Imaging; Mutation; Saccades; Tremor

2012
[L-2 hydroxyglutaric aciduria in a patient with Klinefelter syndrome].
    Neurologia (Barcelona, Spain), 2005, Volume: 20, Issue:2

    Topics: Adolescent; Adult; Amino Acid Metabolism, Inborn Errors; Cerebellar Diseases; Child; Child, Preschool; Female; Glutarates; Humans; Klinefelter Syndrome; Lysine; Magnetic Resonance Imaging; Male

2005
Congenital disorder of glycosylation type 1a: three siblings with a mild neurological phenotype.
    Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia, 2007, Volume: 14, Issue:7

    Topics: Adult; Arginine; Ataxia; Cerebellar Diseases; Congenital Disorders of Glycosylation; Female; Histidine; Humans; Intellectual Disability; Lysine; Magnetic Resonance Imaging; Male; Mutation; Osteoporosis; Phenotype; Phosphotransferases (Phosphomutases); Siblings

2007