lysine has been researched along with Dementia in 12 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (16.67) | 18.7374 |
1990's | 1 (8.33) | 18.2507 |
2000's | 9 (75.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Baas, F; Bourque, PR; Diekstra, FP; Hennekam, EA; Lindhout, D; Ophoff, RA; Schelhaas, HJ; Strengman, E; van den Berg, LH; van Es, MA; Veldink, JH | 1 |
KOREY, SR; SUZUKI, K; TERRY, RD | 1 |
Hanemann, CO; Krause, BJ; Ludolph, AC; Meyer, T; Münch, C; Reske, S; Rosenbohm, A; Sedlmeier, R; Sperfeld, AD; Stumm, G; Uttner, I | 1 |
Aotsuka, A; Fukushi, K; Hirano, S; Irie, T; Kobayashi, T; Ota, T; Shinotoh, H; Tanada, S; Tanaka, N; Tsuboi, Y; Wszolek, ZK | 1 |
Arvanitakis, Z; Boeve, BF; Caviness, JN; Cheshire, WP; Dickson, DW; Hutton, ML; Lin, SC; Liss, JM; Pooley, RA; Slowinski, J; Strongosky, AJ; Tsuboi, Y; Uitti, RJ; Witte, RJ; Wszolek, ZK | 1 |
Azmani, A; Bronner, IF; Heutink, P; Kamphorst, W; Ravid, R; Rizzu, P; Severijnen, LA; van Swieten, JC; Willemsen, R | 1 |
Cantillana, V; Chen, L; Dawson, HN; Vitek, MP | 1 |
Horiuchi, S; Ikeda, K; Kimura, T; Miyakawa, T; Miyata, T; Sobue, G; Takamatsu, J | 1 |
Arima, K; Hasegawa, M; Iwatsubo, T; Kawai, M; Kowalska, A; Mukoyama, M; Sunohara, N; Tabira, T; Takahashi, K; Watanabe, R | 1 |
Kakiuchi, T; Kuhara, S; Nishiyama, S; Takahashi, K; Tonchev, AB; Tsukada, H; Wang, XD; Yamashima, T; Yamashita, J; Zhao, L | 1 |
Baker, M; Brefel-Courbon, C; Delisle, MB; Ferreira, JJ; Ghetti, B; Hutton, M; Murrell, JR; Rascol, O; Tsuboi, Y; Uitti, RJ; Wszolek, ZK | 1 |
Hsia, YE | 1 |
1 review(s) available for lysine and Dementia
Article | Year |
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Inherited hyperammonemic syndromes.
Topics: Acidosis; Amino Acids; Ammonia; Animals; Arginine; Brain; Brain Diseases; Chemical and Drug Induced Liver Injury; Citrulline; Dementia; Homeostasis; Humans; Infant, Newborn; Liver; Lysine; Metabolism, Inborn Errors; Ornithine Carbamoyltransferase; Phosphotransferases; Succinates; Syndrome; Urea; Urease | 1974 |
11 other study(ies) available for lysine and Dementia
Article | Year |
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A case of ALS-FTD in a large FALS pedigree with a K17I ANG mutation.
Topics: Aged; Amino Acid Sequence; Amino Acid Substitution; Amyotrophic Lateral Sclerosis; Base Sequence; Dementia; Female; Heterozygote; Humans; Isoleucine; Lysine; Male; Middle Aged; Mutation; Pedigree; Ribonuclease, Pancreatic | 2009 |
STUDIES ON PROTEIN SYNTHESIS IN BRAIN MICROSOMAL SYSTEM.
Topics: Amino Acids; Biomedical Research; Brain; Brain Diseases; Brain Neoplasms; Dementia; Electrons; Ether; Halothane; Infarction; Lysine; Microscopy; Microscopy, Electron; Microsomes; Pentobarbital; Pharmacology; Proteins; Psychotic Disorders; Radiometry; Rats; Research; Subarachnoid Hemorrhage; Sucrose | 1964 |
Heterozygous R1101K mutation of the DCTN1 gene in a family with ALS and FTD.
Topics: Amyotrophic Lateral Sclerosis; Arginine; Dementia; DNA Mutational Analysis; Dynactin Complex; Family Health; Female; Humans; Lysine; Magnetic Resonance Imaging; Male; Microtubule-Associated Proteins; Middle Aged; Mutation | 2005 |
Brain acetylcholinesterase activity in FTDP-17 studied by PET.
Topics: Acetylcholinesterase; Asparagine; Brain; Chromosomes, Human, Pair 17; Dementia; Frontal Lobe; Humans; Lysine; Male; Microtubule-Associated Proteins; Middle Aged; Mutation; Parkinsonian Disorders; Positron-Emission Tomography; tau Proteins; Temporal Lobe | 2006 |
Clinical-pathologic study of biomarkers in FTDP-17 (PPND family with N279K tau mutation).
Topics: Adult; Asparagine; Cerebral Cortex; Chromosomes, Human, Pair 17; Dementia; Family Health; Female; Fluorodeoxyglucose F18; Humans; Lysine; Male; Middle Aged; Mutation; Neuropsychological Tests; Parkinsonian Disorders; Positron-Emission Tomography; tau Proteins | 2007 |
The DeltaK280 mutation in MAP tau favors exon 10 skipping in vivo.
Topics: Alzheimer Disease; Blotting, Western; Brain; Dementia; Exons; Female; Humans; Immunohistochemistry; Lysine; Microscopy, Electron, Transmission; Middle Aged; Molecular Weight; Mutation; Neurons; Serine; tau Proteins; Trinucleotide Repeat Expansion | 2007 |
The tau N279K exon 10 splicing mutation recapitulates frontotemporal dementia and parkinsonism linked to chromosome 17 tauopathy in a mouse model.
Topics: Age Factors; Analysis of Variance; Animals; Asparagine; Behavior, Animal; Central Nervous System; Chromosomes, Human, Pair 17; Dementia; Embryo, Mammalian; Exons; Gene Expression Regulation, Developmental; Humans; Lysine; Maze Learning; Mice; Mice, Transgenic; Models, Molecular; Motor Activity; Nerve Tissue Proteins; Neurons; Parkinsonian Disorders; RNA Splicing; tau Proteins | 2007 |
Identification of advanced glycation end products of the Maillard reaction in Pick's disease.
Topics: Aged; Arginine; Brain; Dementia; Glycation End Products, Advanced; Humans; Immunohistochemistry; Lysine; Maillard Reaction | 1996 |
Two brothers with frontotemporal dementia and parkinsonism with an N279K mutation of the tau gene.
Topics: Amino Acid Substitution; Asparagine; Codon; Dementia; Diagnosis, Differential; Frontal Lobe; Humans; Lysine; Male; Microscopy, Electron; Middle Aged; Motor Neurons; Mutation, Missense; Neurologic Examination; Neuropsychological Tests; Parkinsonian Disorders; Pedigree; Pyramidal Tracts; Retrospective Studies; tau Proteins; Temporal Lobe | 2000 |
PET imaging of ischemic neuronal death in the hippocampus of living monkeys.
Topics: Affinity Labels; Animals; Azides; Benzodiazepines; Brain Ischemia; Carbon Radioisotopes; Cell Death; Dementia; Disease Models, Animal; Hippocampus; Lysine; Macaca; Maleimides; Neurons; Receptors, GABA-A; Receptors, Muscarinic; Tomography, Emission-Computed | 2002 |
Clinical features and disease haplotypes of individuals with the N279K tau gene mutation: a comparison of the pallidopontonigral degeneration kindred and a French family.
Topics: Adult; Asparagine; Dementia; Exons; Female; Genetic Linkage; Haplotypes; Humans; Lysine; Male; Middle Aged; Mutation, Missense; Pedigree; Supranuclear Palsy, Progressive; tau Proteins | 2002 |