Human Genome Epidemiology Literature Finder
|
Records 1 - 30 (of 35 Records) |
| Query Trace: Amyotrophic Lateral Sclerosis and ANG[original query] |
|---|
| 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 |
| Angiogenin levels and ANG genotypes: dysregulation in amyotrophic lateral sclerosis. PloS one 2010 5 (11): e15402. McLaughlin Russell Lewis, Phukan Julie, McCormack William, Lynch David S, Greenway Matthew, Cronin Simon, Saunders Jean, Slowik Agnieska, Tomik Barbara, Andersen Peter M, Bradley Daniel G, Jakeman Phil, Hardiman Or |
| Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis. Journal of neurology, neurosurgery, and psychiatry 2011 Nov 82 (11): 1239-43. Del Bo R, Tiloca C, Pensato V, Corrado L, Ratti A, Ticozzi N, Corti S, Castellotti B, Mazzini L, Sorarù G, Cereda C, D'Alfonso S, Gellera C, Comi G P, Silani V, |
| Angiogenin variants in Parkinson disease and amyotrophic lateral sclerosis. Annals of neurology 2011 Dec 70 (6): 6. van Es MA, Schelhaas HJ, van Vught PW, Ticozzi N, Andersen PM, Groen EJ, Schulte C, Blauw HM, Koppers M, Diekstra FP, Fumoto K, Leclerc AL, Keagle P, Bloem BR, Scheffer H, van Nuenen BF, van Blitterswijk M, van Rheenen W, Wills AM, Lowe PP, Hu GF, Yu W, Kishikawa H, Wu D, Folkerth RD, Mariani C, Goldwurm S, Pezzoli G, Van Damme P, Lemmens R, Dahlberg C, Birve A, Fernández-Santiago R, Waibel S, Klein C, Weber M, van der Kooi AJ, de Visser M, Verbaan D, van Hilten JJ, Heutink P, Hennekam EA, Cuppen E, Berg D, Brown RH, Silani V, Gasser T, Ludolph AC, Robberecht W, Ophoff RA, Veldink JH, Pasterkamp RJ, de Bakker PI, Landers JE, van de Warrenburg BP, van den Berg LH |
| Oligoclonal bands in the cerebrospinal fluid of amyotrophic lateral sclerosis patients with disease-associated mutations. Journal of neurology 2013 Jan 260 (1): 85-92. Ticozzi Nicola, Tiloca Cinzia, Mencacci Niccolò E, Morelli Claudia, Doretti Alberto, Rusconi Daniela, Colombrita Claudia, Sangalli Davide, Verde Federico, Finelli Palma, Messina Stefano, Ratti Antonia, Silani Vincen |
| 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 |
| Screening of the FUS gene in familial and sporadic amyotrophic lateral sclerosis patients of Chinese origin. European journal of neurology : the official journal of the European Federation of Neurological Societies 2012 Jul 19 (7): 977-83. Zou Z-Y, Peng Y, Feng X-H, Wang X-N, Sun Q, Liu M-S, Li X-G, Cui L |
| SOD1, ANG, TARDBP and FUS mutations in amyotrophic lateral sclerosis: a United States clinical testing lab experience. Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases 2012 Feb 13 (2): 217-22. Brown Jeffrey A, Min Jionghong, Staropoli John F, Collin Elisa, Bi Stephen, Feng Xin, Barone Rosemary, Cao Yi, O'Malley Lei, Xin Winnie, Mullen Thomas E, Sims Katherine |
| Identification of a novel missense mutation in angiogenin in a Chinese amyotrophic lateral sclerosis cohort. Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases 2012 May 13 (3): 270-5. Zou Zhang-Yu, Wang Xin-Ning, Liu Ming-Sheng, Sun Qin, Li Xiao-Guang, Cui Li-Ying, Kong Jimi |
| Lack of unique neuropathology in amyotrophic lateral sclerosis associated with p.K54E angiogenin (ANG) mutation. Neuropathology and applied neurobiology 2013 Aug 39 (5): 562-71. Kirby J, Highley J R, Cox L, Goodall E F, Hewitt C, Hartley J A, Hollinger H C, Fox M, Ince P G, McDermott C J, Shaw P |
| Genetic overlap between apparently sporadic motor neuron diseases. PloS one 2012 7 (11): 11. van Blitterswijk M, Vlam L, van Es MA, van der Pol WL, Hennekam EA, Dooijes D, Schelhaas HJ, van der Kooi AJ, de Visser M, Veldink JH, van den Berg LH |
| Extensive genetics of ALS: a population-based study in Italy. Neurology 2012 Nov 79 (19): 1983-9. Chiò Adriano, Calvo Andrea, Mazzini Letizia, Cantello Roberto, Mora Gabriele, Moglia Cristina, Corrado Lucia, D'Alfonso Sandra, Majounie Elisa, Renton Alan, Pisano Fabrizio, Ossola Irene, Brunetti Maura, Traynor Bryan J, Restagno Gabriella, |
| Screening of the SOD1, FUS, TARDBP, ANG, and OPTN mutations in Korean patients with familial and sporadic ALS. Neurobiology of aging 2012 May 33 (5): 1017.e17-23. Kwon Min-Jung, Baek Wonki, Ki Chang-Seok, Kim Hyun Young, Koh Seong-Ho, Kim Jong-Won, Kim Seung Hy |
| 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 |
| Mutational analysis of angiogenin gene in Parkinson's disease. PloS one 2014 9 (11): e112661. Chen Meng-Ling, Wu Ruey-Meei, Tai Chun-Hwei, Lin Chin-Hsi |
| Association between the Angiogenin (ANG) K17I variant and amyotrophic lateral sclerosis risk in Caucasian: a meta-analysis. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2015 Aug . Pan Lishou, Deng Xinbo, Ding Dan, Leng Huilin, Zhu Xuepeng, Wang Zhe |
| [The association between angiogenin gene variations and familial amyotrophic lateral sclerosis in Chinese Han patients]. Zhonghua nei ke za zhi 2015 Feb 54 (2): 122-4. Zhang Huagang, Zhang Yingshuang, Tang Lu, Zhang Nan, Fan Dongshe |
| Genetic studies of Russian patients with amyotrophic lateral sclerosis. Amyotrophic lateral sclerosis & frontotemporal degeneration 2015 Nov 1-7. Lysogorskaia Elena V, Abramycheva Nataliya Yu, Zakharova Mariya N, Stepanova Mariya S, Moroz Anna A, Rossokhin Alexey V, Illarioshkin Sergey |
| Large-scale screening in sporadic amyotrophic lateral sclerosis identifies genetic modifiers in C9orf72 repeat carriers. Neurobiology of aging 2015 Dec . Dekker Annelot M, Seelen Meinie, van Doormaal Perry T C, van Rheenen Wouter, Bothof Reinoud J P, van Riessen Tim, Brands William J, van der Kooi Anneke J, de Visser Marianne, Voermans Nicol C, Pasterkamp R Jeroen, Veldink Jan H, van den Berg Leonard H, van Es Michael |
| Lack of association between the Angiogenin (ANG) rs11701 polymorphism and amyotrophic lateral sclerosis risk: a meta-analysis. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2016 Jan . Pan Li-Shou, Deng Xin-Bo, Wang Zheng, Leng Hui-Lin, Zhu Xue-Peng, Ding D |
| Comprehensive targeted next-generation sequencing in Japanese familial amyotrophic lateral sclerosis. Neurobiology of aging 2017 05 53 194.e1-194.e8. Nishiyama Ayumi, Niihori Tetsuya, Warita Hitoshi, Izumi Rumiko, Akiyama Tetsuya, Kato Masaaki, Suzuki Naoki, Aoki Yoko, Aoki Masas |
| Insights into the role of ribonuclease 4 polymorphisms in amyotrophic lateral sclerosis. Journal of biomolecular structure & dynamics 2017 12 37 (1): 116-130. Padhi Aditya K, Narain Priyam, Dave Upma, Satija Rohit, Patir Anirudh, Gomes Jam |
| Targeted next-generation sequencing reveals novel and rare variants in Indian patients with amyotrophic lateral sclerosis. Neurobiology of aging 2018 May . Narain Priyam, Pandey Ashutosh, Gupta Shruti, Gomes James, Bhatia Rohit, Vivekanandan Perum |
| Identification and characterization of novel and rare susceptible variants in Indian amyotrophic lateral sclerosis patients. Neurogenetics 2019 8 20 (4): 197-208. Narain Priyam, Padhi Aditya K, Dave Upma, Mishra Dibyakanti, Bhatia Rohit, Vivekanandan Perumal, Gomes Jam |
| Angiogenin mutations in Hungarian patients with amyotrophic lateral sclerosis: Clinical, genetic, computational, and functional analyses. Brain and behavior 2019 Apr e01293. Tripolszki Kornélia, Danis Judit, Padhi Aditya K, Gomes James, Bozó Renáta, Nagy Zsófia F, Nagy Dóra, Klivényi Péter, Engelhardt József I, Széll Már |
| Comparison of the clinical and genetic features of amyotrophic lateral sclerosis across Cuban, Uruguayan and Irish clinic-based populations. Journal of neurology, neurosurgery, and psychiatry 2019 3 90 (6): 659-665. Ryan Marie, Zaldívar Vaillant Tatiana, McLaughlin Russell L, Doherty Mark A, Rooney James, Heverin Mark, Gutierrez Joel, Lara-Fernández Gloria Esther, Pita Rodríguez Mariana, Hackembruch Jochen, Perna Abayubá, Vazquez Maria Cristina, Musio Marco, Ketzoian Carlos N, Logroscino Giancarlo, Hardiman Or |
| Assessment of ANG variants in Parkinson's disease. Neurobiology of aging 2021 Mar . Grenn Francis P, Moore Anni, Bandres-Ciga Sara, Krohn Lynne, Blauwendraat Cornelis, |
| Exome Sequencing of a Portuguese Cohort of Frontotemporal Dementia Patients: Looking Into the ALS-FTD Continuum. Frontiers in neurology 2022 13 886379. Tábuas-Pereira Miguel, Santana Isabel, Gibbons Elizabeth, Paquette Kimberly, Almeida Maria Rosário, Baldeiras Inês, Bras Jose, Guerreiro Ri |
| Neural stem cell homeostasis is affected in cortical organoids carrying a mutation in Angiogenin. The Journal of pathology 2024 1 . Ross Ferguson, Michael A van Es, Leonard H van den Berg, Vasanta Subramani |
- Page last reviewed:Feb 1, 2024
- Content source: