Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Counseling and ATXN2[original query] |
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Contribution of major amyotrophic lateral sclerosis genes to the etiology of sporadic disease. Neurology 2012 Jul 79 (1): 66-72. Lattante Serena, Conte Amelia, Zollino Marcella, Luigetti Marco, Del Grande Alessandra, Marangi Giuseppe, Romano Angela, Marcaccio Alessandro, Meleo Emiliana, Bisogni Giulia, Rossini Paolo Maria, Sabatelli Mar |
ATAXIN2 CAG-repeat length in Italian patients with amyotrophic lateral sclerosis: risk factor or variant phenotype? Implication for genetic testing and counseling. Neurobiology of aging 2012 Aug 33 (8): 1847.e15-21. Gellera Cinzia, Ticozzi Nicola, Pensato Viviana, Nanetti Lorenzo, Castucci Alessia, Castellotti Barbara, Lauria Giuseppe, Taroni Franco, Silani Vincenzo, Mariotti Cateri |
Extensive molecular genetic survey of Taiwanese patients with amyotrophic lateral sclerosis. Neurobiology of aging 2014 Oct 35 (10): 2423.e1-6. Soong Bing-Wen, Lin Kon-Ping, Guo Yuh-Cherng, Lin Chou-Ching K, Tsai Pei-Chien, Liao Yi-Chu, Lu Yi-Chun, Wang Shuu-Jiun, Tsai Ching-Piao, Lee Yi-Chu |
Amyotrophic lateral sclerosis risk for spinocerebellar ataxia type 2 ATXN2 CAG repeat alleles: a meta-analysis. JAMA neurology 2014 Dec 71 (12): 1529-34. Neuenschwander Annalese G, Thai Khanh K, Figueroa Karla P, Pulst Stefan |
The repeat length of C9orf72 is associated with the survival of amyotrophic lateral sclerosis patients without C9orf72 pathological expansions. Frontiers in neurology 2022 8 13 939775. Tang Lu, Chen Lu, Liu Xiaolu, He Ji, Ma Yan, Zhang Nan, Fan Dongshe |
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