methionine has been researched along with Dementia in 14 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (7.14) | 18.2507 |
2000's | 5 (35.71) | 29.6817 |
2010's | 7 (50.00) | 24.3611 |
2020's | 1 (7.14) | 2.80 |
Authors | Studies |
---|---|
Chen, S; Hata, J; Honda, T; Isa, A; Katakura, Y; Kitazono, T; Mihara, A; Nakao, T; Ninomiya, T; Ohara, T; Shimizu, K; Tamrakar, S; Wang, D; Yonemoto, K | 1 |
Fratiglioni, L; Hooshmand, B; Kalpouzos, G; Kåreholt, I; Kivipelto, M; Mangialasche, F; Refsum, H; Smith, AD; von Arnim, CAF | 1 |
Allegri, RF; Bartoloni, L; Pletnikova, O; Riudavets, MA; Schultz, M; Sevlever, G; St George-Hyslop, P; Troncoso, JC | 1 |
Asgari Mobarake, K; Keshavarz, P; Leili, EK; Rezaei, S; Saberi, A | 1 |
Prakash, A; Singh, M | 1 |
Bae, KY; Kim, JM; Kim, SW; Park, KH; Shin, IS; Stewart, R; Yang, SJ; Yoon, JS | 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 |
Domínguez, A; Graus, F; Nos, C; Saiz, A; Sanchez-Valle, R; Yagüe, J | 1 |
Bugiani, O; Catania, M; Di Fede, G; Farina, L; Giaccone, G; Marcon, G; Morbin, M; Rossi, G; Sacco, L; Tagliavini, F | 1 |
Giraudier, S; Michot, JM; Papo, T; Sedel, F; Smiejan, JM | 1 |
Ayache, N; Brandel, JP; Dormont, D; Faucheux, BA; Galanaud, D; Haïk, S; Hauw, JJ; Linguraru, MG; Peoc'h, K; Privat, N | 1 |
Panini, R; Salvioli, G; Scarpetta, G; Ventura, P; Verlato, C | 1 |
Gottfries, CG; Regland, B | 1 |
14 other study(ies) available for methionine and Dementia
Article | Year |
---|---|
Association of serum s-adenosylmethionine, s-adenosylhomocysteine, and their ratio with the risk of dementia and death in a community.
Topics: Dementia; Humans; Methionine; Proportional Hazards Models; S-Adenosylhomocysteine; S-Adenosylmethionine | 2022 |
Association of Methionine to Homocysteine Status With Brain Magnetic Resonance Imaging Measures and Risk of Dementia.
Topics: Aged; Aged, 80 and over; Atrophy; Biomarkers; Brain; Case-Control Studies; Dementia; Female; Homocysteine; Humans; Incidence; Longitudinal Studies; Magnetic Resonance Imaging; Male; Methionine; Middle Aged; Organ Size; Risk Factors; Sweden | 2019 |
Familial dementia with frontotemporal features associated with M146V presenilin-1 mutation.
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 |
Brain-derived neurotrophic factor (BDNF) Val66Met polymorphism and post-stroke dementia: a hospital-based study from northern Iran.
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 |
Possible role of endothelin receptor against hyperhomocysteinemia and β-amyloid induced AD type of vascular dementia in rats.
Topics: Alzheimer Disease; Amyloid beta-Peptides; Animals; Bosentan; Brain; Dementia; Dementia, Vascular; Endothelins; Endothelium, Vascular; Hyperhomocysteinemia; Lipid Peroxidation; Male; Maze Learning; Memory; Methionine; Mitochondria; Oxidative Stress; Rats; Rats, Wistar; Receptors, Endothelin; Sulfonamides | 2017 |
Role of BDNF val66met polymorphism on the association between physical activity and incident dementia.
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 |
Elevated phosphorylated tau pT-181 in a possible PRNP codon 129 MV vCJD case.
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.
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 |
Clinical and genetic features of human prion diseases in Catalonia: 1993-2002.
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 |
Familial frontotemporal dementia associated with the novel MAPT mutation T427M.
Topics: Aged; Dementia; DNA Mutational Analysis; Family Health; Female; Humans; Magnetic Resonance Imaging; Methionine; Mutation; tau Proteins; Threonine | 2005 |
Psychosis, paraplegia and coma revealing methylenetetrahydrofolate reductase deficiency in a 56-year-old woman.
Topics: Brain; Brain Diseases, Metabolic, Inborn; Catatonia; Chromosome Aberrations; Chromosomes, Human, Pair 1; Coma; Dementia; Exons; Folic Acid; Genes, Recessive; Homocysteine; Humans; Magnetic Resonance Imaging; Methionine; Methylenetetrahydrofolate Reductase (NADPH2); Mutation, Missense; Neurologic Examination; Paraplegia; Polymorphism, Genetic; Psychotic Disorders | 2008 |
In vivo detection of thalamic gliosis: a pathoradiologic demonstration in familial fatal insomnia.
Topics: Alleles; Brain; Codon; Dementia; Diffusion Magnetic Resonance Imaging; DNA Mutational Analysis; Gliosis; Homozygote; Humans; Insomnia, Fatal Familial; Magnetic Resonance Spectroscopy; Male; Methionine; Middle Aged; Neurologic Examination; Neuropsychological Tests; Polysomnography; Prion Proteins; Prions; Thalamic Diseases; Thalamus | 2008 |
Hyperhomocysteinemia and related factors in 600 hospitalized elderly subjects.
Topics: Aged; Aged, 80 and over; Aging; Dementia; Diabetes Complications; Fasting; Female; Homocysteine; Humans; Hyperhomocysteinemia; Inflammatory Bowel Diseases; Kinetics; Linear Models; Male; Methionine; Nutrition Disorders; Odds Ratio; Renal Insufficiency; Vascular Diseases | 2001 |
Slowed synthesis of DNA and methionine is a pathogenetic mechanism common to dementia in Down's syndrome, AIDS and Alzheimer's disease?
Topics: AIDS Dementia Complex; Alzheimer Disease; Amyloidosis; Cell Death; Dementia; DNA; DNA Repair; DNA Replication; Down Syndrome; Humans; Methionine; Models, Biological | 1992 |