glycine and Amentia
glycine has been researched along with Amentia in 10 studies
Research Excerpts
| Excerpt | Relevance | Reference |
|---|---|---|
| "To study parkinsonism, dementia, dystonia, and amyotrophy as subphenotypes of SCA2, and to explore the effect of CAG repeats at different loci and of mitochondrial polymorphism A10398G as modifiers of phenotype." | 1.46 | Neurological phenotypes in spinocerebellar ataxia type 2: Role of mitochondrial polymorphism A10398G and other risk factors. ( Augustin, MC; Barsottini, O; Jardim, LB; Locks-Coelho, LD; Monte, TL; Pedroso, JL; Pereira, FS; Reckziegel, EDR; Santos, ASP; Saraiva-Pereira, ML; Vargas, FR, 2017) |
Research
Studies (10)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (20.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 6 (60.00) | 29.6817 |
| 2010's | 2 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
Authors
| Authors | Studies |
|---|---|
| Monte, TL | 1 |
| Pereira, FS | 1 |
| Reckziegel, EDR | 1 |
| Augustin, MC | 1 |
| Locks-Coelho, LD | 1 |
| Santos, ASP | 1 |
| Pedroso, JL | 1 |
| Barsottini, O | 1 |
| Vargas, FR | 1 |
| Saraiva-Pereira, ML | 1 |
| Jardim, LB | 1 |
| Djamshidian, A | 1 |
| Schaefer, J | 1 |
| Haubenberger, D | 1 |
| Stogmann, E | 1 |
| Zimprich, F | 1 |
| Auff, E | 1 |
| Zimprich, A | 1 |
| Arnold, SE | 1 |
| Vega, IE | 1 |
| Karlawish, JH | 1 |
| Wolk, DA | 1 |
| Nunez, J | 1 |
| Negron, M | 1 |
| Xie, SX | 1 |
| Wang, LS | 1 |
| Dubroff, JG | 1 |
| McCarty-Wood, E | 1 |
| Trojanowski, JQ | 2 |
| Van Deerlin, V | 1 |
| Saunders-Pullman, R | 1 |
| Lipton, RB | 1 |
| Senthil, G | 1 |
| Katz, M | 1 |
| Costan-Toth, C | 1 |
| Derby, C | 1 |
| Bressman, S | 1 |
| Verghese, J | 1 |
| Ozelius, LJ | 1 |
| Dächsel, JC | 1 |
| Ross, OA | 1 |
| Mata, IF | 1 |
| Kachergus, J | 1 |
| Toft, M | 1 |
| Cannon, A | 1 |
| Baker, M | 1 |
| Adamson, J | 1 |
| Hutton, M | 1 |
| Dickson, DW | 1 |
| Farrer, MJ | 1 |
| Spina, S | 1 |
| Murrell, JR | 1 |
| Yoshida, H | 1 |
| Ghetti, B | 1 |
| Bermingham, N | 1 |
| Sweeney, B | 1 |
| Dlouhy, SR | 1 |
| Crowther, RA | 1 |
| Goedert, M | 1 |
| Keohane, C | 1 |
| Gaig, C | 1 |
| Ezquerra, M | 1 |
| Martí, MJ | 1 |
| Valldeoriola, F | 1 |
| Muñoz, E | 1 |
| Lladó, A | 1 |
| Rey, MJ | 1 |
| Cardozo, A | 1 |
| Molinuevo, JL | 1 |
| Tolosa, E | 1 |
| Van Deerlin, VM | 1 |
| Leverenz, JB | 1 |
| Bekris, LM | 1 |
| Bird, TD | 1 |
| Yuan, W | 1 |
| Elman, LB | 1 |
| Clay, D | 1 |
| Wood, EM | 1 |
| Chen-Plotkin, AS | 1 |
| Martinez-Lage, M | 1 |
| Steinbart, E | 1 |
| McCluskey, L | 1 |
| Grossman, M | 1 |
| Neumann, M | 1 |
| Wu, IL | 1 |
| Yang, WS | 1 |
| Kalb, R | 1 |
| Galasko, DR | 1 |
| Montine, TJ | 1 |
| Lee, VM | 1 |
| Schellenberg, GD | 1 |
| Yu, CE | 1 |
| Pomara, N | 1 |
| Banay-Schwartz, M | 1 |
| Block, R | 1 |
| Stanley, M | 1 |
| Gershon, S | 1 |
| Smith, CC | 1 |
| Bowen, DM | 1 |
| Francis, PT | 1 |
| Snowden, JS | 1 |
| Neary, D | 1 |
Other Studies
10 other studies available for glycine and Amentia
| Article | Year |
|---|---|
Neurological phenotypes in spinocerebellar ataxia type 2: Role of mitochondrial polymorphism A10398G and other risk factors.
Topics: Adult; Aged; Alanine; Ataxin-2; Dementia; Dystonia; Female; Genetic Predisposition to Disease; Glyci | 2017 |
A novel mutation in the VCP gene (G157R) in a German family with inclusion-body myopathy with Paget disease of bone and frontotemporal dementia.
Topics: Adenosine Triphosphatases; Adult; Arginine; Cell Cycle Proteins; Dementia; DNA Mutational Analysis; | 2009 |
Frequency and clinicopathological characteristics of presenilin 1 Gly206Ala mutation in Puerto Rican Hispanics with dementia.
Topics: Aged; Aged, 80 and over; Alanine; Dementia; Female; Gene Frequency; Genetic Carrier Screening; Glyci | 2013 |
Increased frequency of the LRRK2 G2019S mutation in an elderly Ashkenazi Jewish population is not associated with dementia.
Topics: Aged, 80 and over; Aging; Dementia; DNA Mutational Analysis; Female; Glycine; Humans; Jews; Leucine- | 2006 |
Lrrk2 G2019S substitution in frontotemporal lobar degeneration with ubiquitin-immunoreactive neuronal inclusions.
Topics: Aged; Amino Acid Substitution; Dementia; Female; Glycine; Humans; Inclusion Bodies; Leucine-Rich Rep | 2007 |
The novel Tau mutation G335S: clinical, neuropathological and molecular characterization.
Topics: Adult; Dementia; DNA Mutational Analysis; Glycine; Humans; Male; Microscopy, Electron, Transmission; | 2007 |
Screening for the LRRK2 G2019S and codon-1441 mutations in a pathological series of parkinsonian syndromes and frontotemporal lobar degeneration.
Topics: Dementia; DNA Mutational Analysis; Female; Genetic Predisposition to Disease; Genetic Testing; Glyci | 2008 |
TARDBP mutations in amyotrophic lateral sclerosis with TDP-43 neuropathology: a genetic and histopathological analysis.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Alanine; Amyotrophic Lateral Sclerosis; Brain; Child; De | 2008 |
Elevation of RBC glycine and choline levels in geriatric patients treated with lithium.
Topics: Aged; Alzheimer Disease; Choline; Cognition Disorders; Dementia; Erythrocytes; Female; Glycine; Huma | 1983 |
Putative amino acid transmitters in lumbar cerebrospinal fluid of patients with histologically verified Alzheimer's dementia.
Topics: Adult; Aged; Alzheimer Disease; Amino Acids; Aspartic Acid; Dementia; Epilepsy; Female; Glutamates; | 1985 |