glycine has been researched along with Dementia in 10 studies
Dementia: An acquired organic mental disorder with loss of intellectual abilities of sufficient severity to interfere with social or occupational functioning. The dysfunction is multifaceted and involves memory, behavior, personality, judgment, attention, spatial relations, language, abstract thought, and other executive functions. The intellectual decline is usually progressive, and initially spares the level of consciousness.
| 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) |
| 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 | 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 |
10 other studies available for glycine and Dementia
| 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 |