arginine and Abnormal Movements

arginine has been researched along with Abnormal Movements 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	0 (0.00)	29.6817
2010's	2 (100.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Bilińska, ZT; Labib, S; Mazurkiewicz, L; Małek, LA; Płoski, R; Saj, M; Tesson, F	1
Groffen, AJ; Hilgevoord, AA; Linssen, WH; Tijssen, MA; van Rootselaar, AF; van Strien, TW	1

Other Studies

2 other study(ies) available for arginine and Abnormal Movements

Article	Year
A new c.1621 C > G, p.R541G lamin A/C mutation in a family with DCM and regional wall motion abnormalities (akinesis/dyskinesis): genotype-phenotype correlation. Journal of human genetics, 2011, Volume: 56, Issue:1 Topics: Amino Acid Substitution; Arginine; Cardiomyopathy, Dilated; Dyskinesias; Family; Genetic Association Studies; Glycine; Humans; Lamin Type A; Male; Mutation; Pedigree; Polymorphism, Single Nucleotide; Thoracic Wall; Young Adult	2011
Paroxysmal kinesigenic dyskinesia: cortical or non-cortical origin. Parkinsonism & related disorders, 2012, Volume: 18, Issue:5 Topics: Adolescent; Arginine; Chromosomes, Human, Pair 16; Codon, Terminator; DNA Mutational Analysis; Dyskinesias; Dystonia; Electroencephalography; Epilepsy, Benign Neonatal; Family Health; Female; Humans; Image Processing, Computer-Assisted; Magnetic Resonance Imaging; Male; Membrane Proteins; Mutation; Nerve Tissue Proteins; Seizures	2012

Article

Year

A new c.1621 C > G, p.R541G lamin A/C mutation in a family with DCM and regional wall motion abnormalities (akinesis/dyskinesis): genotype-phenotype correlation.

Journal of human genetics, 2011, Volume: 56, Issue:1

Topics: Amino Acid Substitution; Arginine; Cardiomyopathy, Dilated; Dyskinesias; Family; Genetic Association Studies; Glycine; Humans; Lamin Type A; Male; Mutation; Pedigree; Polymorphism, Single Nucleotide; Thoracic Wall; Young Adult

2011

Paroxysmal kinesigenic dyskinesia: cortical or non-cortical origin.

Parkinsonism & related disorders, 2012, Volume: 18, Issue:5

Topics: Adolescent; Arginine; Chromosomes, Human, Pair 16; Codon, Terminator; DNA Mutational Analysis; Dyskinesias; Dystonia; Electroencephalography; Epilepsy, Benign Neonatal; Family Health; Female; Humans; Image Processing, Computer-Assisted; Magnetic Resonance Imaging; Male; Membrane Proteins; Mutation; Nerve Tissue Proteins; Seizures

2012