arginine and Chorea

arginine has been researched along with Chorea in 2 studies

Research

Studies (2)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	2 (100.00)	29.6817
2010's	0 (0.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Fuchs, O; Pfarr, N; Pohlenz, J; Schmidt, H	1
Asmus, F; Chinnery, PF; Devlin, A; Gasser, T; Munz, M; Zimprich, A	1

Other Studies

2 other study(ies) available for arginine and Chorea

Article	Year
Elevated serum triiodothyronine and intellectual and motor disability with paroxysmal dyskinesia caused by a monocarboxylate transporter 8 gene mutation. Developmental medicine and child neurology, 2009, Volume: 51, Issue:3 Topics: Arginine; Child; Chorea; Developmental Disabilities; DNA Mutational Analysis; Enzyme-Linked Immunosorbent Assay; Histidine; Humans; Intellectual Disability; Magnetic Resonance Imaging; Male; Monocarboxylic Acid Transporters; Mutation; Symporters; Triiodothyronine	2009
Clinical differentiation of genetically proven benign hereditary chorea and myoclonus-dystonia. Movement disorders : official journal of the Movement Disorder Society, 2007, Oct-31, Volume: 22, Issue:14 Topics: Adolescent; Arginine; Child; Chorea; DNA Mutational Analysis; Dystonic Disorders; Exons; Family Health; Female; Genotype; Glycine; Humans; Male; Mutation; Myoclonus; Nuclear Proteins; Sarcoglycans; Thyroid Nuclear Factor 1; Transcription Factors; Valine	2007

Article

Year

Elevated serum triiodothyronine and intellectual and motor disability with paroxysmal dyskinesia caused by a monocarboxylate transporter 8 gene mutation.

Developmental medicine and child neurology, 2009, Volume: 51, Issue:3

Topics: Arginine; Child; Chorea; Developmental Disabilities; DNA Mutational Analysis; Enzyme-Linked Immunosorbent Assay; Histidine; Humans; Intellectual Disability; Magnetic Resonance Imaging; Male; Monocarboxylic Acid Transporters; Mutation; Symporters; Triiodothyronine

2009

Clinical differentiation of genetically proven benign hereditary chorea and myoclonus-dystonia.

Movement disorders : official journal of the Movement Disorder Society, 2007, Oct-31, Volume: 22, Issue:14

Topics: Adolescent; Arginine; Child; Chorea; DNA Mutational Analysis; Dystonic Disorders; Exons; Family Health; Female; Genotype; Glycine; Humans; Male; Mutation; Myoclonus; Nuclear Proteins; Sarcoglycans; Thyroid Nuclear Factor 1; Transcription Factors; Valine

2007