Compounds > asparagine

asparagine and Dementia

asparagine has been researched along with Dementia in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19901 (12.50)18.7374
1990's0 (0.00)18.2507
2000's7 (87.50)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Hayashi, M; Ishihara, T; Kidani, T; Kobayashi, K; Koshino, Y; Kuroda, S; Miyazu, K; Ujike, H1
Hayashi, M; Iijima, M; Ishihara, T; Kidani, T; Kobayashi, K; Koshino, Y; Kuroda, S; Nakano, H; Shimazaki, M; Sugimori, K; Ujike, H1
Aotsuka, A; Fukushi, K; Hirano, S; Irie, T; Kobayashi, T; Ota, T; Shinotoh, H; Tanada, S; Tanaka, N; Tsuboi, Y; Wszolek, ZK1
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, ZK1
Cantillana, V; Chen, L; Dawson, HN; Vitek, MP1
Arima, K; Hasegawa, M; Iwatsubo, T; Kawai, M; Kowalska, A; Mukoyama, M; Sunohara, N; Tabira, T; Takahashi, K; Watanabe, R1
Baker, M; Brefel-Courbon, C; Delisle, MB; Ferreira, JJ; Ghetti, B; Hutton, M; Murrell, JR; Rascol, O; Tsuboi, Y; Uitti, RJ; Wszolek, ZK1
Wilde, KM1

Other Studies

8 other study(ies) available for asparagine and Dementia

ArticleYear
Another phenotype of frontotemporal dementia and parkinsonism linked to chromosome-17 (FTDP-17) with a missense mutation of S305N closely resembling Pick's disease.
    Journal of neurology, 2003, Volume: 250, Issue:8

    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.
    Dementia and geriatric cognitive disorders, 2004, Volume: 17, Issue:4

    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.
    Neurology, 2006, Apr-25, Volume: 66, Issue:8

    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).
    Parkinsonism & related disorders, 2007, Volume: 13, Issue:4

    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.
    The Journal of neuroscience : the official journal of the Society for Neuroscience, 2007, Aug-22, Volume: 27, Issue:34

    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.
    Neurology, 2000, May-09, Volume: 54, Issue:9

    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
Clinical features and disease haplotypes of individuals with the N279K tau gene mutation: a comparison of the pallidopontonigral degeneration kindred and a French family.
    Archives of neurology, 2002, Volume: 59, Issue:6

    Topics: Adult; Asparagine; Dementia; Exons; Female; Genetic Linkage; Haplotypes; Humans; Lysine; Male; Middle Aged; Mutation, Missense; Pedigree; Supranuclear Palsy, Progressive; tau Proteins

2002
[Comments on a geriatric drug].
    Zeitschrift fur Allgemeinmedizin, 1974, Feb-28, Volume: 50, Issue:6

    Topics: Aged; Asparagine; Aspartic Acid; Dementia; Drug Combinations; Female; Hematoporphyrins; Humans; Magnesium; Male; Orotic Acid; Potassium; Procaine

1974