Compounds > valine

valine and Dementia

valine has been researched along with Dementia in 15 studies

Research

Studies (15)

Timeframe	Studies, this research(%)	All Research%
pre-1990	0 (0.00)	18.7374
1990's	0 (0.00)	18.2507
2000's	6 (40.00)	29.6817
2010's	9 (60.00)	24.3611
2020's	0 (0.00)	2.80

Authors

Authors	Studies
Estevez-Fraga, C; López-Sendón Moreno, JL; Zeun, P	1
Allegri, RF; Bartoloni, L; Pletnikova, O; Riudavets, MA; Schultz, M; Sevlever, G; St George-Hyslop, P; Troncoso, JC	1
Feng, GF; Han, H; Hu, XD; Liu, Y; Qian, YH; Shi, LL; Yang, WN	1
Asgari Mobarake, K; Keshavarz, P; Leili, EK; Rezaei, S; Saberi, A	1
Barzilai, N; Derby, CA; Katz, M; Lipton, RB; Ozelius, L; Sanders, AE; Wang, C	1
Bae, KY; Kim, JM; Kim, SW; Park, KH; Shin, IS; Stewart, R; Yang, SJ; Yoon, JS	1
Ferrell, R; Fiocco, AJ; Harris, TB; Li, R; Lindquist, K; Nalls, M; Simonsick, EM; Yaffe, K	1
Andrews, MM; Bishop, MT; Chohan, G; Green, AJ; Knight, RS; McCord, Y; McKenzie, JM; Pennington, C	1
Bonasera, SJ; Boxer, AL; Cholfin, JA; Crawford, RK; Gennatas, ED; Gorno-Tempini, ML; Karydas, A; Kramer, JH; Miller, BL; Rankin, KP; Rosen, HJ; Sasaki, DA; Seeley, WW; Weiner, M; Zhou, J	1
Baker, M; Berry, RW; Bigio, EH; Binder, LI; Davies, P; de Silva, R; Demirci, S; Dickson, D; Espinoza, M; Gamblin, TC; Grover, A; Grujic, ZM; Guillozet, AL; Herzog, LL; Hogg, M; Hutton, M; Ishizawa, T; LaPointe, NE; Lees, A; Mesulam, MM; Sahara, N; Sweet, AP; Weintraub, S; Yen, SH	1
Domínguez, A; Graus, F; Nos, C; Saiz, A; Sanchez-Valle, R; Yagüe, J	1
Barquero, MS; Ginestal, RC; Güell, I; Guerrero, C; Jimenez-Escrig, A; Montero, T; Orensanz, L; Rabano, A; Simon, J	1
Armendariz, J; Behrens, MI; Budde, J; Cairns, NJ; Chakraverty, S; Gitcho, M; Goate, AM; Hinrichs, AL; Kauwe, JS; Levitch, D; Liscic, RM; Morris, JC; Mukherjee, O; Norton, J; Pastor, P; Shears, S; Taylor-Reinwald, L; Tenenholz Grinberg, L; Tu, PH	1
Chatterjee, A; Crowe, A; Farmer, JM; Forman, MS; Grossman, M; Joyce, S; Lee, VM; Trojanowski, JQ; Van Deerlin, VM	1
Amici, S; Arning, E; Bottiglieri, T; Gallai, V; Lanari, A; Ortiz, T; Parnetti, L	1

Reviews

1 review(s) available for valine and Dementia

Article	Year
Current Methods for the Treatment and Prevention of Drug-Induced Parkinsonism and Tardive Dyskinesia in the Elderly. Drugs & aging, 2018, Volume: 35, Issue:11 Topics: Aged; Dementia; Dyskinesia, Drug-Induced; Humans; Parkinsonian Disorders; Risk Factors; Tardive Dyskinesia; Tetrabenazine; Valine	2018

Other Studies

14 other study(ies) available for valine and Dementia

Article	Year
Familial dementia with frontotemporal features associated with M146V presenilin-1 mutation. Brain pathology (Zurich, Switzerland), 2013, Volume: 23, Issue:5 Topics: Adult; Dementia; DNA Mutational Analysis; Electroencephalography; Family Health; Female; Frontal Lobe; Humans; Inclusion Bodies; Magnetic Resonance Imaging; Male; Methionine; Middle Aged; Neuropsychological Tests; Plaque, Amyloid; Presenilin-1; Temporal Lobe; Tomography Scanners, X-Ray Computed; Valine	2013
The effects of valsartan on cognitive deficits induced by aluminum trichloride and d-galactose in mice. Neurological research, 2014, Volume: 36, Issue:7 Topics: Acetylcholinesterase; Aluminum Chloride; Aluminum Compounds; Animals; Cerebral Cortex; Chlorides; Cognition Disorders; Dementia; Disease Models, Animal; Galactose; Glutathione Peroxidase; Hippocampus; Malondialdehyde; Maze Learning; Memory Disorders; Mice; Nootropic Agents; Oxidative Stress; Random Allocation; Superoxide Dismutase; Tetrazoles; Valine; Valsartan	2014
Brain-derived neurotrophic factor (BDNF) Val66Met polymorphism and post-stroke dementia: a hospital-based study from northern Iran. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2016, Volume: 37, Issue:6 Topics: Aged; Aged, 80 and over; Brain-Derived Neurotrophic Factor; Chi-Square Distribution; Dementia; DNA Mutational Analysis; Female; Genotype; Hospitals; Humans; Iran; Male; Methionine; Middle Aged; Polymorphism, Single Nucleotide; Proportional Hazards Models; Risk Factors; Severity of Illness Index; Stroke; Valine	2016
Association of a functional polymorphism in the cholesteryl ester transfer protein (CETP) gene with memory decline and incidence of dementia. JAMA, 2010, Jan-13, Volume: 303, Issue:2 Topics: Aged; Aged, 80 and over; Alzheimer Disease; Cholesterol Ester Transfer Proteins; Dementia; Female; Genetic Predisposition to Disease; Genotype; Humans; Incidence; Male; Memory Disorders; New York; Polymorphism, Single Nucleotide; Prospective Studies; Valine	2010
Role of BDNF val66met polymorphism on the association between physical activity and incident dementia. Neurobiology of aging, 2011, Volume: 32, Issue:3 Topics: Activities of Daily Living; Aged; Aged, 80 and over; Brain-Derived Neurotrophic Factor; Cognition Disorders; Dementia; Female; Genome-Wide Association Study; Genotype; Humans; Incidence; Logistic Models; Male; Methionine; Motor Activity; Polymorphism, Single Nucleotide; Republic of Korea; Retrospective Studies; Statistics, Nonparametric; Valine	2011
COMT genotype and cognitive function: an 8-year longitudinal study in white and black elders. Neurology, 2010, Apr-20, Volume: 74, Issue:16 Topics: Age Factors; Aged; Aging; Amino Acid Sequence; Amino Acid Substitution; Black People; Brain Chemistry; Catechol O-Methyltransferase; Cognition Disorders; Cytoprotection; Dementia; DNA Mutational Analysis; Dopamine; Female; Gene Expression Regulation, Enzymologic; Gene Frequency; Genetic Markers; Genetic Predisposition to Disease; Genetic Testing; Genotype; Humans; Longitudinal Studies; Male; Neuropsychological Tests; Racial Groups; Time Factors; Valine; White People	2010
Elevated phosphorylated tau pT-181 in a possible PRNP codon 129 MV vCJD case. Journal of neurology, neurosurgery, and psychiatry, 2010, Volume: 81, Issue:12 Topics: 14-3-3 Proteins; Adult; Amino Acid Substitution; Blotting, Western; Brain; Codon; Creutzfeldt-Jakob Syndrome; Dementia; Enzyme-Linked Immunosorbent Assay; Gene Expression; Genetic Carrier Screening; Humans; Magnetic Resonance Imaging; Male; Methionine; Nerve Growth Factors; Phosphorylation; Prion Proteins; Prions; Pulvinar; S100 Calcium Binding Protein beta Subunit; S100 Proteins; tau Proteins; Threonine; Valine	2010
COMT Val158Met genotype influences neurodegeneration within dopamine-innervated brain structures. Neurology, 2012, May-22, Volume: 78, Issue:21 Topics: Aged; Alleles; Alzheimer Disease; Catechol O-Methyltransferase; Cerebral Cortex; Dementia; Dopamine; Female; Frontotemporal Dementia; Frontotemporal Lobar Degeneration; Genotype; Humans; Magnetic Resonance Imaging; Male; Methionine; Middle Aged; Polymorphism, Single Nucleotide; Prefrontal Cortex; Valine	2012
The L266V tau mutation is associated with frontotemporal dementia and Pick-like 3R and 4R tauopathy. Acta neuropathologica, 2003, Volume: 106, Issue:4 Topics: Adult; Antibodies, Monoclonal; Blotting, Western; Brain; Dementia; DNA Mutational Analysis; Exons; Family Health; Humans; Immunohistochemistry; In Vitro Techniques; Leucine; Male; Microscopy, Electron; Microtubules; Mutation; Pick Disease of the Brain; Protein Isoforms; Receptors, Endothelin; Reverse Transcriptase Polymerase Chain Reaction; RNA, Messenger; tau Proteins; Tauopathies; Time Factors; Valine	2003
Clinical and genetic features of human prion diseases in Catalonia: 1993-2002. European journal of neurology, 2004, Volume: 11, Issue:10 Topics: 14-3-3 Proteins; Adult; Aged; Aged, 80 and over; Amyloid; Ataxia; Dementia; Electroencephalography; Female; Humans; Magnetic Resonance Imaging; Male; Methionine; Middle Aged; Polymorphism, Genetic; Prion Diseases; Prion Proteins; Prions; Protein Precursors; Retrospective Studies; Spain; Valine	2004
New V272A presenilin 1 mutation with very early onset subcortical dementia and parkinsonism. European journal of neurology, 2004, Volume: 11, Issue:10 Topics: Adult; Alanine; Amyloid beta-Peptides; Brain; Dementia; DNA Mutational Analysis; Family Health; Female; Humans; Immunohistochemistry; Lewy Bodies; Magnetic Resonance Imaging, Cine; Membrane Proteins; Middle Aged; Mutation, Missense; Nerve Tissue Proteins; Neurofibrillary Tangles; Neuropsychological Tests; Parkinsonian Disorders; Peptide Fragments; Postmortem Changes; Presenilin-1; Synucleins; Valine	2004
HDDD2 is a familial frontotemporal lobar degeneration with ubiquitin-positive, tau-negative inclusions caused by a missense mutation in the signal peptide of progranulin. Annals of neurology, 2006, Volume: 60, Issue:3 Topics: Adult; Aged; Aged, 80 and over; Aspartic Acid; Chromosomes, Human, Pair 17; Dementia; DNA Mutational Analysis; Family Health; Female; Genetic Predisposition to Disease; Humans; Immunohistochemistry; Inclusion Bodies; Intercellular Signaling Peptides and Proteins; Male; Middle Aged; Mutation, Missense; Neuropsychological Tests; tau Proteins; Ubiquitin; Valine	2006
Biochemical and pathological characterization of frontotemporal dementia due to a Leu266Val mutation in microtubule-associated protein tau in an African American individual. Acta neuropathologica, 2007, Volume: 113, Issue:4 Topics: Adult; Black or African American; Dementia; DNA-Binding Proteins; Family Health; Female; Humans; Leucine; Magnetic Resonance Imaging; Mutation; Neuropsychological Tests; Polycomb-Group Proteins; tau Proteins; Transcription Factors; Valine	2007
Plasma total homocysteine levels and the C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene: a study in an Italian population with dementia. Mechanisms of ageing and development, 2001, Volume: 122, Issue:16 Topics: Aged; Alanine; Dementia; Female; Folic Acid; Homocysteine; Humans; Italy; Male; Methylenetetrahydrofolate Reductase (NADPH2); Oxidoreductases Acting on CH-NH Group Donors; Point Mutation; Valine; Vitamin B 12	2001