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Records 1-5

Query Trace: Atrophy and GBA[original query]

Posterior Cortical Atrophy phenotype in a GBA N370S mutation carrier: a case report. BMC neurology 2021 Jan 21 (1): 17. Picillo Marina, Scannapieco Sara, Iavarone Alessandro, Ginevrino Monia, Valente Enza Maria, Barone Pao Similar articles in PubMed
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 Similar articles in PubMed
Cerebral Imaging Markers of GBA and LRRK2 Related Parkinson's Disease and Their First-Degree Unaffected Relatives. Brain topography 2018 May . Thaler Avner, Kliper Efrat, Maidan Inbal, Herman Talia, Rosenberg-Katz Keren, Bregman Noa, Gurevich Tanya, Shiner Tamara, Hausdorff Jeffrey M, Orr-Urtreger Avi, Giladi Nir, Mirelman An Similar articles in PubMed
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 Similar articles in PubMed
Genetic association study of glucocerebrosidase gene L444P mutation in essential tremor and multiple system atrophy in mainland. 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 Similar articles in PubMed

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