asparagine has been researched along with Parkinsonian Disorders in 7 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 6 (85.71) | 29.6817 |
2010's | 1 (14.29) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Hattori, N; Li, Y; Motoi, Y; Nakanishi, A; Ogaki, K; Shimizu, N; Takanashi, M; Tomiyama, H; Yokoyama, K | 1 |
Hayashi, M; Ishihara, T; Kidani, T; Kobayashi, K; Koshino, Y; Kuroda, S; Miyazu, K; Ujike, H | 1 |
Hayashi, M; Iijima, M; Ishihara, T; Kidani, T; Kobayashi, K; Koshino, Y; Kuroda, S; Nakano, H; Shimazaki, M; Sugimori, K; Ujike, H | 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 |
Cantillana, V; Chen, L; Dawson, HN; Vitek, MP | 1 |
Arima, K; Hasegawa, M; Iwatsubo, T; Kawai, M; Kowalska, A; Mukoyama, M; Sunohara, N; Tabira, T; Takahashi, K; Watanabe, R | 1 |
7 other study(ies) available for asparagine and Parkinsonian Disorders
Article | Year |
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Visual grasping in frontotemporal dementia and parkinsonism linked to chromosome 17 (microtubule-associated with protein tau): a comparison of N-Isopropyl-p-[(123)I]-iodoamphetamine brain perfusion single photon emission computed tomography analysis with
Topics: Adult; Aged; Asparagine; Benzamides; Brain; Chromosomes, Human, Pair 17; Female; Hand Strength; Humans; Lysine; Male; Middle Aged; Parkinsonian Disorders; Pyrrolidines; Supranuclear Palsy, Progressive; tau Proteins; Tomography, Emission-Computed, Single-Photon | 2011 |
Another phenotype of frontotemporal dementia and parkinsonism linked to chromosome-17 (FTDP-17) with a missense mutation of S305N closely resembling Pick's disease.
Topics: Asparagine; Chromosomes, Human, Pair 17; Dementia; Dentate Gyrus; Genetic Linkage; Humans; Immunohistochemistry; Inclusion Bodies; Male; Microscopy, Electron; Middle Aged; Mutation, Missense; Parkinsonian Disorders; Phenotype; Pick Disease of the Brain; Serine; tau Proteins | 2003 |
Pick's disease pathology of a missense mutation of S305N of frontotemporal dementia and parkinsonism linked to chromosome 17: another phenotype of S305N.
Topics: Asparagine; Base Sequence; Brain; Dementia; DNA Mutational Analysis; Genetic Linkage; Heterozygote; Humans; Immunohistochemistry; Magnetic Resonance Imaging; Male; Microscopy, Electron; Middle Aged; Mutation, Missense; Parkinsonian Disorders; Phenotype; Pick Disease of the Brain; Polymorphism, Restriction Fragment Length; Serine; tau Proteins | 2004 |
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 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 |
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 |