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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Sep 13, 2024. (Total: 231440Documents)
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Records 1 - 6 (of 6 Records)

Query Trace: Lewy Body Disease and GBA[original query]
The neurobiology of glucocerebrosidase-associated parkinsonism: a positron emission tomography study of dopamine synthesis and regional cerebral blood flow.
Brain : a journal of neurology 2012 Aug 135 (Pt 8): Pt 8.
Goker-Alpan O, Masdeu JC, Kohn PD, Ianni A, Lopez G, Groden C, Chapman MC, Cropp B, Eisenberg DP, Maniwang ED, Davis J, Wiggs E, Sidransky E, Berman KF
GBA mutations increase risk for Lewy body disease with and without Alzheimer disease pathology.
Neurology 2012 Oct .
Tsuang D, Leverenz JB, Lopez OL, Hamilton RL, Bennett DA, Schneider JA, Buchman AS, Larson EB, Crane PK, Kaye JA, Kramer P, Woltjer R, Kukull W, Nelson PT, Jicha GA, Neltner JH, Galasko D, Masliah E, Trojanowski JQ, Schellenberg GD, Yearout D, Huston H, Fritts-Penniman A, Mata IF, Wan JY, Edwards KL, Montine TJ, Zabetian CP
Serum lipid alterations in GBA-associated Parkinson's disease.
Parkinsonism & related disorders 2017 9 44 58-65.
Guedes Leonor Correia, Chan Robin Barry, Gomes Marcos António, Conceição Vasco A, Machado Raquel Bouça, Soares Tiago, Xu Yimeng, Gaspar Paulo, Carriço Joao André, Alcalay Roy N, Ferreira Joaquim J, Outeiro Tiago Fleming, Miltenberger-Miltenyi Gabri
GBA variation and susceptibility to multiple system atrophy.
Parkinsonism & related disorders 2020 Jun 77 64-69.
Wernick Anna I, Walton Ronald L, Koga Shunsuke, Soto-Beasley Alexandra I, Heckman Michael G, Gan-Or Ziv, Ren Yingxue, Rademakers Rosa, Uitti Ryan J, Wszolek Zbigniew K, Cheshire William P, Dickson Dennis W, Ross Owen
Clinicopathologic and genetic features of multiple system atrophy with Lewy body disease.
Brain pathology (Zurich, Switzerland) 2020 4 30 (4): 766-778.
Koga Shunsuke, Li Fuyao, Zhao Na, Roemer Shanu F, Ferman Tanis J, Wernick Anna I, Walton Ronald L, Faroqi Ayman H, Graff-Radford Neill R, Cheshire William P, Ross Owen A, Dickson Dennis
Frequency of Parkinson's Disease Genes and Role of PARK2 in Amyotrophic Lateral Sclerosis: An NGS Study.
Genes 2022 Jul 13 (8): .
Vacchiano Veria, Bartoletti-Stella Anna, Rizzo Giovanni, Avoni Patrizia, Parchi Piero, Salvi Fabrizio, Liguori Rocco, Capellari Sabi
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