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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 6 (of 6 Records)

Query Trace: Counseling and TARDBP[original query]
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
PFN1 mutations are also rare in the Catalan population with amyotrophic lateral sclerosis.
Journal of neurology 2014 Dec 261 (12): 2387-92.
Syriani Enrique, Salvans Candi, Salvadó Maria, Morales Miguel, Lorenzo Laura, Cazorla Sonia, Gamez Jos
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
Rare, low-frequency and common coding variants of ARHGEF28 gene and their association with sporadic amyotrophic lateral sclerosis.
Neurobiology of aging 2019 Mar .
Song Yang, Lin Feng, Ye Cheng-Hui, Huang Huaping, Li Xuying, Yao Xiaoli, Xu Yanming, Wang Chaodo
Clinico-genetic findings in 509 frontotemporal dementia patients.
Molecular psychiatry 2021 Sep .
Wagner Matias, Lorenz Georg, Volk Alexander E, Brunet Theresa, Edbauer Dieter, Berutti Riccardo, Zhao Chen, Anderl-Straub Sarah, Bertram Lars, Danek Adrian, Deschauer Marcus, Dill Veronika, Fassbender Klaus, Fliessbach Klaus, Götze Katharina S, Jahn Holger, Kornhuber Johannes, Landwehrmeyer Bernhard, Lauer Martin, Obrig Hellmuth, Prudlo Johannes, Schneider Anja, Schroeter Matthias L, Uttner Ingo, Vukovich Ruth, Wiltfang Jens, Winkler Andrea S, Zhou Qihui, Ludolph Albert C, , Oexle Konrad, Otto Markus, Diehl-Schmid Janine, Winkelmann Julia
Unveiling the SOD1-mediated ALS phenotype: insights from a comprehensive meta-analysis.
Journal of neurology 2023 11 .
Teuta Domi, Paride Schito, Giacomo Sferruzza, Tommaso Russo, Laura Pozzi, Federica Agosta, Paola Carrera, Nilo Riva, Massimo Filippi, Angelo Quattrini, Yuri Matteo Falzo
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