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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Sep 25, 2023. (Total: 221440Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Tauopathies and LRRK2[original query]
Screening for the LRRK2 G2019S and codon-1441 mutations in a pathological series of parkinsonian syndromes and frontotemporal lobar degeneration.
Journal of the neurological sciences 2008 Jul 270 (1-2): 94-8.
Gaig Carles, Ezquerra Mario, Martí Maria José, Valldeoriola Francesc, Muñoz Esteban, Lladó Albert, Rey Maria Jesús, Cardozo Adriana, Molinuevo José Luis, Tolosa Eduar
Study of LRRK2 variation in tauopathy: Progressive supranuclear palsy and corticobasal degeneration.
Movement disorders : official journal of the Movement Disorder Society 2016 Oct .
Sanchez-Contreras Monica, Heckman Michael G, Tacik Pawel, Diehl Nancy, Brown Patricia H, Soto-Ortolaza Alexandra I, Christopher Elizabeth A, Walton Ronald L, Ross Owen A, Golbe Lawrence I, Graff-Radford Neill, Wszolek Zbigniew K, Dickson Dennis W, Rademakers Ro
Genetic determinants of survival in progressive supranuclear palsy: a genome-wide association study. GWAS Catalog
The Lancet. Neurology 2020 12 20 (2): 107-116.
Jabbari Edwin, Koga Shunsuke, Valentino Rebecca R, Reynolds Regina H, Ferrari Raffaele, Tan Manuela M X, Rowe James B, Dalgard Clifton L, Scholz Sonja W, Dickson Dennis W, Warner Thomas T, Revesz Tamas, Höglinger Günter U, Ross Owen A, Ryten Mina, Hardy John, Shoai Maryam, Morris Huw R,
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