HuGE Literature Finder
Records
1
-
7
| Genetics of validated Parkinson's disease subtypes in the Oxford Discovery and Tracking Parkinson's cohorts. Journal of neurology, neurosurgery, and psychiatry 2022 Jun . Lawton Michael, Tan Manuela Mx, Ben-Shlomo Yoav, Baig Fahd, Barber Thomas, Klein Johannes C, Evetts Samuel G, Millin Stephanie, Malek Naveed, Grosset Katherine, Barker Roger A, Williams Nigel, Burn David J, Foltynie Thomas, Morris Huw R, Wood Nicholas, Grosset Donald G, Hu Michele Tao-Mi |
| 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 |
| Evolution of prodromal parkinsonian features in a cohort of GBA mutation-positive individuals: a 6-year longitudinal study. Journal of neurology, neurosurgery, and psychiatry 2019 6 90 (10): 1091-1097. Avenali Micol, Toffoli Marco, Mullin Stephen, McNeil Alisdair, Hughes Derralynn A, Mehta A, Blandini Fabio, Schapira Anthony H |
| Frequency of GBA variants in autopsy-proven multiple system atrophy. Movement disorders clinical practice 2017 10 4 (4): 574-581. Sklerov Miriam, Kang Un Jung, Liong Christopher, Clark Lorraine, Marder Karen, Pauciulo Michael, Nichols William C, Chung Wendy K, Honig Lawrence S, Cortes Etty, Vonsattel Jean Paul, Alcalay Roy |
| Variants associated with Gaucher disease in multiple system atrophy. Annals of clinical and translational neurology 2015 Apr 2 (4): 417-26. Mitsui Jun, Matsukawa Takashi, Sasaki Hidenao, Yabe Ichiro, Matsushima Masaaki, Dürr Alexandra, Brice Alexis, Takashima Hiroshi, Kikuchi Akio, Aoki Masashi, Ishiura Hiroyuki, Yasuda Tsutomu, Date Hidetoshi, Ahsan Budrul, Iwata Atsushi, Goto Jun, Ichikawa Yaeko, Nakahara Yasuo, Momose Yoshio, Takahashi Yuji, Hara Kenju, Kakita Akiyoshi, Yamada Mitsunori, Takahashi Hitoshi, Onodera Osamu, Nishizawa Masatoyo, Watanabe Hirohisa, Ito Mizuki, Sobue Gen, Ishikawa Kinya, Mizusawa Hidehiro, Kanai Kazuaki, Hattori Takamichi, Kuwabara Satoshi, Arai Kimihito, Koyano Shigeru, Kuroiwa Yoshiyuki, Hasegawa Kazuko, Yuasa Tatsuhiko, Yasui Kenichi, Nakashima Kenji, Ito Hijiri, Izumi Yuishin, Kaji Ryuji, Kato Takeo, Kusunoki Susumu, Osaki Yasushi, Horiuchi Masahiro, Kondo Tomoyoshi, Murayama Shigeo, Hattori Nobutaka, Yamamoto Mitsutoshi, Murata Miho, Satake Wataru, Toda Tatsushi, Filla Alessandro, Klockgether Thomas, Wüllner Ullrich, Nicholson Garth, Gilman Sid, Tanner Caroline M, Kukull Walter A, Stern Mathew B, Lee Virginia M-Y, Trojanowski John Q, Masliah Eliezer, Low Phillip A, Sandroni Paola, Ozelius Laurie J, Foroud Tatiana, Tsuji Sho |
| Genetic association study of glucocerebrosidase gene L444P mutation in essential tremor and multiple system atrophy in mainland China. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2012 Nov . Sun QY, Guo JF, Han WW, Zuo X, Wang L, Yao LY, Pan Q, Xia K, Yan XX, Tang BS |
- Page last reviewed:Feb 1, 2023
- Page last updated:Mar 22, 2023
- Content source: