arginine has been researched along with Parkinsonian Disorders in 13 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 8 (61.54) | 29.6817 |
| 2010's | 5 (38.46) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bui, LC; Dairou, J; Lamouri, A; Leger, T; Mihoub, M; Richarme, G | 1 |
| Behari, M; Kirola, L; Shishir, C; Thelma, BK | 1 |
| Bonifati, V; Farrer, MJ; Ferreira, JJ; Griffith, A; Haugarvoll, K; Kachergus, J; Latsoudis, H; Lin, CH; Plaitakis, A; Ross, OA; Sampaio, C; Spanaki, C; Wu, RM; Zabetian, CP | 1 |
| Fu, Y; Song, C; Wan, Q; Zeng, Y; Zhang, K | 1 |
| Fish, M; Hack, M; Majounie, E; Morris, HR; Newsway, V; Rohrer, JD; Warren, JD; Williams, N | 1 |
| Chang, MY; Jo, AY; Kim, BW; Kim, CH; Kim, D; Kim, KS; Ko, JY; Koh, HC; Lanza, R; Lee, H; Lee, SH; Lee, YS; Park, CH; Rhee, YH; Shim, JW; Suh, W; Yi, SH | 1 |
| Arai, H; Fujihara, K; Ichinose, H; Itoyama, Y; Kikuchi, A; Kimpara, T; Nagai, M; Okamura, N; Shiga, Y; Takeda, A; Tanji, H; Urano, F | 1 |
| Bounds, R; Chen, J; Farrer, M; Gwinn-Hardy, K; Hulihan, M; Hwu, WL; Lin, CH; Lincoln, S; Wu, RM | 1 |
| Elsaesser, VE; Foroud, T; Halter, CA; Marek, DK; Nichols, WC; Pankratz, N; Pauciulo, MW; Rudolph, A; Shults, CW; Wojcieszek, J | 1 |
| Alvarez-Alvarez, M; Ciordia, R; de Pancorbo, MM; Farrer, MJ; Gómez-Busto, F; Gómez-Esteban, JC; González-Fernández, MC; Lezcano, E; Mata, IF; Rodríguez-Martínez, MB; Ross, OA; Velasco, F; Zarranz, JJ | 1 |
| Amos, LA; Fan, J; Gasparini, L; Goedert, M; Golding, M; Magnani, E; Schiavo, G; Spillantini, MG; Williams, M | 1 |
| Abbruzzese, G; Barone, P; Bonuccelli, U; Colao, A; Cossu, G; Donati, E; Eleopra, R; Epifanio, A; Longo, K; Lucetti, C; Manfredi, M; Marchese, R; Marconi, R; Morgante, L; Pellecchia, MT; Petrone, A; Pivonello, R; Scaravilli, T; Sensi, M | 1 |
| Benecke, R; Berg, D; Bonifati, V; Brown, L; Cras, P; De Deyn, PP; Engelborghs, S; Farrer, MJ; Foroud, T; Gaig, C; Gasser, T; Gibson, JM; Goldwurm, S; Guidi, M; Hagenah, J; Haugarvoll, K; Kachergus, JM; Klein, C; Nichols, WC; Nuytemans, K; Pals, P; Pickut, B; Rademakers, R; Riboldazzi, G; Ross, OA; Samii, A; Tan, EK; Theuns, J; Tolosa, E; Uitti, RJ; Van Broeckhoven, C; Walter, U; Wszolek, ZK; Zabetian, CP | 1 |
1 trial(s) available for arginine and Parkinsonian Disorders
| Article | Year |
|---|---|
The comparison of clonidine, arginine and both combined: a growth hormone stimulation test to differentiate multiple system atrophy from idiopathic Parkinson's disease.
Topics: Aged; Arginine; Clonidine; Diagnosis, Differential; Drug Combinations; Female; Human Growth Hormone; Humans; Male; Multiple System Atrophy; Parkinsonian Disorders; Sensitivity and Specificity; Up-Regulation | 2010 |
12 other study(ies) available for arginine and Parkinsonian Disorders
| Article | Year |
|---|---|
Parkinsonism-associated protein DJ-1/Park7 is a major protein deglycase that repairs methylglyoxal- and glyoxal-glycated cysteine, arginine, and lysine residues.
Topics: Acetylcysteine; Albumins; Apoptosis; Arginine; Aspartate Aminotransferases; Catalysis; Cell Survival; Cysteine; Escherichia coli; Fructose-Bisphosphate Aldolase; Glucose; Glycolates; Glyoxal; Humans; Intracellular Signaling Peptides and Proteins; Lactates; Lysine; Mass Spectrometry; Oncogene Proteins; Oxidative Stress; Parkinsonian Disorders; Protein Deglycase DJ-1; Pyruvaldehyde | 2015 |
Identification of a novel homozygous mutation Arg459Pro in SYNJ1 gene of an Indian family with autosomal recessive juvenile Parkinsonism.
Topics: Adult; Arginine; DNA Mutational Analysis; Family Health; Female; Genes, Recessive; Humans; India; Magnetic Resonance Imaging; Male; Mutation; Parkinsonian Disorders; Phenotype; Phosphoric Monoester Hydrolases; Proline; Young Adult | 2016 |
Haplotype analysis of Lrrk2 R1441H carriers with parkinsonism.
Topics: Adult; Arginine; DNA Mutational Analysis; Female; Gene Frequency; Genetic Predisposition to Disease; Haplotypes; Histidine; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Middle Aged; Parkinsonian Disorders; Polymorphism, Single Nucleotide; Protein Serine-Threonine Kinases | 2009 |
Perry syndrome due to the DCTN1 G71R mutation: a distinctive levodopa responsive disorder with behavioral syndrome, vertical gaze palsy, and respiratory failure.
Topics: Arginine; Behavioral Symptoms; DNA Mutational Analysis; Dopamine Agents; Dynactin Complex; Glycine; Humans; Levodopa; Male; Microtubule-Associated Proteins; Middle Aged; Neuropsychological Tests; Optic Nerve Diseases; Parkinsonian Disorders; Respiratory Insufficiency | 2010 |
Protein-based human iPS cells efficiently generate functional dopamine neurons and can treat a rat model of Parkinson disease.
Topics: Animals; Apoptosis; Arginine; Cell Differentiation; Cell Line; Cell Lineage; Cellular Reprogramming; Cellular Senescence; Dopamine; Gene Expression Regulation, Developmental; Genes, p53; Genetic Vectors; Humans; Induced Pluripotent Stem Cells; Kruppel-Like Factor 4; Kruppel-Like Transcription Factors; Lentivirus; Neurons; Octamer Transcription Factor-3; Parkinsonian Disorders; Proto-Oncogene Proteins c-myc; Rats; Retroviridae; SOXB1 Transcription Factors; Tumor Suppressor Protein p53 | 2011 |
Arg(184)His mutant GTP cyclohydrolase I, causing recessive hyperphenylalaninemia, is responsible for dopa-responsive dystonia with parkinsonism: a case report.
Topics: Antiparkinson Agents; Arginine; Brain; Dystonia; Genes, Recessive; GTP Cyclohydrolase; Humans; Levodopa; Magnetic Resonance Imaging; Male; Middle Aged; Parkinsonian Disorders; Pedigree; Phenylketonurias; Point Mutation; Tomography, Emission-Computed; Tomography, Emission-Computed, Single-Photon | 2004 |
Parkin mutations and early-onset parkinsonism in a Taiwanese cohort.
Topics: Adult; Arginine; Cohort Studies; DNA Mutational Analysis; Exons; Family Health; Female; Glycine; Humans; Male; Middle Aged; Mutation; Neurologic Examination; Parkinsonian Disorders; Pedigree; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; Taiwan; Ubiquitin-Protein Ligases | 2005 |
Mutations in DJ-1 are rare in familial Parkinson disease.
Topics: Aged; Aged, 80 and over; Arginine; Exons; Female; Glutamic Acid; Humans; Intracellular Signaling Peptides and Proteins; Lod Score; Male; Middle Aged; Mutation; Oncogene Proteins; Parkinsonian Disorders; Protein Deglycase DJ-1; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger | 2006 |
Lrrk2-associated parkinsonism is a major cause of disease in Northern Spain.
Topics: Adult; Aged; Arginine; DNA Mutational Analysis; Family Health; Female; Genetic Predisposition to Disease; Glycine; Humans; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Middle Aged; Mutation; Parkinsonian Disorders; Protein Serine-Threonine Kinases; Serine; Spain | 2007 |
Interaction of tau protein with the dynactin complex.
Topics: Animals; Arginine; Axons; Cloning, Molecular; Dynactin Complex; Humans; Mice; Microtubule-Associated Proteins; Models, Biological; Mutation; Neurons; Parkinsonian Disorders; Protein Binding; Protein Structure, Tertiary; tau Proteins; Two-Hybrid System Techniques | 2007 |
The arginine growth hormone stimulation test in bradykinetic-rigid parkinsonisms.
Topics: Aged; Analysis of Variance; Arginine; Female; Human Growth Hormone; Humans; Male; Middle Aged; Multiple System Atrophy; Parkinson Disease; Parkinsonian Disorders; ROC Curve | 2008 |
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease.
Topics: Adult; Aged; Aged, 80 and over; Amino Acid Substitution; Arginine; Cysteine; DNA Mutational Analysis; Female; Glycine; Haplotypes; Humans; Internationality; Leucine-Rich Repeat Serine-Threonine Protein Kinase-2; Male; Middle Aged; Parkinson Disease; Parkinsonian Disorders; Protein Serine-Threonine Kinases; Serine | 2008 |