Human Genome Epidemiology Literature Finder
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Records 1 - 11 (of 11 Records) |
| Query Trace: Amyotrophic Lateral Sclerosis and VAPB[original query] |
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| Sporadic ALS is not associated with VAPB gene mutations in Southern Italy. Journal of negative results in biomedicine 2006 5 (): 7. Conforti Francesca Luisa, Sprovieri Teresa, Mazzei Rosalucia, Ungaro Carmine, Tessitore Alessandro, Tedeschi Gioacchino, Patitucci Alessandra, Magariello Angela, Gabriele Annalia, Labella Vincenzo, Simone Isabella Laura, Majorana Giovanni, Monsurrò Maria Rosaria, Valentino Paola, Muglia Maria, Quattrone Al |
| SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations. Journal of medical genetics 2010 Aug 47 (8): 554-60. Millecamps Stéphanie, Salachas François, Cazeneuve Cécile, Gordon Paul, Bricka Bernard, Camuzat Agnès, Guillot-Noël Léna, Russaouen Odile, Bruneteau Gaëlle, Pradat Pierre-François, Le Forestier Nadine, Vandenberghe Nadia, Danel-Brunaud Véronique, Guy Nathalie, Thauvin-Robinet Christel, Lacomblez Lucette, Couratier Philippe, Hannequin Didier, Seilhean Danielle, Le Ber Isabelle, Corcia Philippe, Camu William, Brice Alexis, Rouleau Guy, LeGuern Eric, Meininger Vince |
| FUS, TARDBP, and SOD1 mutations in a Taiwanese cohort with familial ALS. Neurobiology of aging 2011 Mar 32 (3): 553.e13-21. Tsai Ching-Paio, Soong Bing-Wen, Lin Kon-Ping, Tu Pang-Hsien, Lin Jer-Li, Lee Yi-Chu |
| VAPB and C9orf72 mutations in 1 familial amyotrophic lateral sclerosis patient. Neurobiology of aging 2012 Dec 33 (12): 2950.e1-4. van Blitterswijk Marka, van Es Michael A, Koppers Max, van Rheenen Wouter, Medic Jelena, Schelhaas Helenius J, van der Kooi Anneke J, de Visser Marianne, Veldink Jan H, van den Berg Leonard |
| No association between VAPB mutations and familial or sporadic ALS in Sweden, Portugal and Iceland. Amyotrophic lateral sclerosis & frontotemporal degeneration 2013 Dec 14 (7-8): 620-7. Ingre Caroline, Pinto Susana, Birve Anna, Press Rayomand, Danielsson Olof, de Carvalho Mamede, Gu?mundsson Grétar, Andersen Peter |
| Identify mutation in amyotrophic lateral sclerosis cases using HaloPlex target enrichment system. Neurobiology of aging 2014 Dec 35 (12): 2881.e11-5. Liu Zhi-Jun, Li Hong-Fu, Tan Guo-He, Tao Qing-Qing, Ni Wang, Cheng Xue-Wen, Xiong Zhi-Qi, Wu Zhi-Yi |
| Genetic analysis of patients with familial and sporadic amyotrophic lateral sclerosis in a Brazilian Research Center. Amyotrophic lateral sclerosis & frontotemporal degeneration 2016 Dec 1-7. Chadi Gerson, Maximino Jessica Ruivo, Jorge Frederico Mennucci de Haidar, Borba FabríCIO Castro dE, Gilio Joyce Meire, Callegaro Dagoberto, Lopes Camila GalvãO, Santos Samantha Nakamura Dos, Rebelo Gabriela Natania Sal |
| Different gene expression profiles in iPSC-derived motor neurons from ALS8 patients with variable clinical courses suggest mitigating pathways for neurodegeneration. Human molecular genetics 2020 4 29 (9): 1465-1475. Oliveira Danyllo, Morales-Vicente David A, Amaral Murilo S, Luz Livia, Sertié Andrea L, Leite Felipe S, Navarro Claudia, Kaid Carolini, Esposito Joyce, Goulart Ernesto, Caires Luiz, Alves Luciana M, Melo Uirá S, Figueiredo Thalita, Mitne-Neto Miguel, Okamoto Oswaldo K, Verjovski-Almeida Sergio, Zatz Maya |
| Genetic epidemiology of familial ALS in Brazil. Neurobiology of aging 2021 2 102 227.e1-227.e4. Nunes Gonçalves João Pedro, Leoni Tauana Bernardes, Martins Melina Pazian, Peluzzo Thiago Mazzo, Dourado Mario Emílio T, Saute Jonas Alex M, Paranhos Miranda Covaleski Anna Paula, Bulle de Oliveira Acary Souza, Claudino Rinaldo, Marques Wilson, Nucci Anamarli, França Marcondes |
| A comparative study of cognitive and behavioral profiles between sporadic and type 8 amyotrophic lateral sclerosis. Muscle & nerve 2023 7 . Cássia de Alcântara, Marcelo Maroco Cruzeiro, Marcondes Cavalcante França, Mariana Asmar Alencar, Antônio Jaeger, Caroline Martins de Araújo, Natália Araújo Sundfeld da Gama, Sarah Teixeira Camargos, Leonardo Cruz de Sou |
| Increased copy-number variant load of associated risk genes in sporadic cases of amyotrophic lateral sclerosis. Cellular and molecular life sciences : CMLS 2024 7 81 (1): 316. Maria Guarnaccia, Giovanna Morello, Valentina La Cognata, Vincenzo La Bella, Francesca Luisa Conforti, Sebastiano Cavalla |
- Page last reviewed:Feb 1, 2024
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