Human Genome Epidemiology Literature Finder
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Records 1 - 15 (of 15 Records) |
| Query Trace: Disease and SCN9A[original query] |
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| A role of SCN9A in human epilepsies, as a cause of febrile seizures and as a potential modifier of Dravet syndrome. PLoS genetics 2009 Sep 5 (9): e1000649. Singh Nanda A, Pappas Chris, Dahle E Jill, Claes Lieve R F, Pruess Timothy H, De Jonghe Peter, Thompson Joel, Dixon Missy, Gurnett Christina, Peiffer Andy, White H Steve, Filloux Francis, Leppert Mark |
| Contribution of genetic variants to pain susceptibility in Parkinson disease. European journal of pain (London, England) 2012 Oct 16 (9): 1243-50. Greenbaum L, Tegeder I, Barhum Y, Melamed E, Roditi Y, Djaldetti |
| [Association between mutations of SCN9A gene and pain related to Parkinsonism]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2013 Feb 30 (1): 17-20. Zhang Li-mei, Chen Yong-qian, Li Wan-jun, Sun Wei, Huang Yue, Zou Hai-qia |
| SCN9A Variants May be Implicated in Neuropathic Pain Associated With Diabetic Peripheral Neuropathy and Pain Severity. The Clinical journal of pain 2015 Jan . Li Qingqin S, Cheng Peter, Favis Reyna, Wickenden Alan, Romano Gary, Wang H |
| Depression and Catechol-O-methyltransferase (COMT) genetic variants are associated with pain in Parkinson's disease. Scientific reports 2017 Jul 7 (1): 6306. Lin Chin-Hsien, Chaudhuri K Ray, Fan Jun-Yu, Ko Chia-I, Rizos Alexandra, Chang Chia-Wen, Lin Han-I, Wu Yih- |
| Na channel variants in patients with painful and nonpainful peripheral neuropathy. Neurology. Genetics 2017 Dec 3 (6): e207. Wadhawan Samir, Pant Saumya, Golhar Ryan, Kirov Stefan, Thompson John, Jacobsen Leslie, Qureshi Irfan, Ajroud-Driss Senda, Freeman Roy, Simpson David M, Smith A Gordon, Hoke Ahmet, Bristow Linda |
| Homozygosity for the SCN10A Polymorphism rs6795970 Is Associated With Hypoalgesic Inflammatory Bowel Disease Phenotype. Frontiers in medicine 2018 12 5 324. Gonzalez-Lopez Eugene, Imamura Kawasawa Yuka, Walter Vonn, Zhang Lijun, Koltun Walter A, Huang Xuemei, Vrana Kent E, Coates Matthew |
| No Association of Polymorphisms in Nav1.7 or Nerve Growth Factor Receptor Genes with Trigeminal Neuralgia. Pain medicine (Malden, Mass.) 2018 Oct . Costa Grazielle Mara Ferreira, Rocha Luiz Paulo C, Siqueira Silvia Regina Dowgan Tesseroli de, Moreira Paula Rocha, Almeida-Leite Camila Mega |
| Comprehensive Exonic Sequencing of Known Ataxia Genes in Episodic Ataxia. Biomedicines 2020 5 8 (5): . Maksemous Neven, Sutherland Heidi G, Smith Robert A, Haupt Larisa M, Griffiths Lyn |
| Fibromyalgia: A Review of Related Polymorphisms and Clinical Relevance. Anais da Academia Brasileira de Ciencias 2021 11 93 (suppl 4): e20210618. Janssen Luísa P, Medeiros Liciane F, Souza Andressa DE, Silva Juliana |
| Genetic associated complications of type 2 diabetes mellitus. Panminerva medica 2021 10 64 (2): 274-288. Wong Yee H, Wong Shen H, Wong Xiao T, Yap Qiao Y, Yip Khar Y, Wong Liang Z, Chellappan Dinesh K, Bhattamisra Subrat K, Candasamy Mayur |
| Methylome analysis of ALS patients and presymptomatic mutation carriers in blood cells. Neurobiology of aging 2022 5 116 16-24. Ruf Wolfgang P, Hannon Eilis, Freischmidt Axel, Grozdanov Veselin, Brenner David, Müller Kathrin, Knehr Antje, Günther Kornelia, Dorst Johannes, Ammerpohl Ole, Danzer Karin M, Mill Jonathan, Ludolph Albert C, Weishaupt Jochen |
| Whole genome sequencing in adults with clinical hallmarks of hypophosphatasia negative for ALPL variants. Molecular biology reports 2024 9 51 (1): 984. Lothar Seefried, Anna Petryk, Guillermo Del Angel, Felix Reder, Peter Bau |
| Genetic exploration of Dravet syndrome: two case report. Journal of medical case reports 2024 4 18 (1): 215. Agung Triono, Elisabeth Siti Herini, Guna |
| Genetic associations of neuropathic pain and sensory profile in a deeply phenotyped neuropathy cohort. Pain 2024 10 . Mikael Åkerlund, Georgios Baskozos, Wenqianglong Li, Andreas C Themistocleous, Mathilde M V Pascal, N William Rayner, Nadine Attal, Ralf Baron, Sophie Baudic, Kristine Bennedsgaard, Didier Bouhassira, Maddalena Comini, Geert Crombez, Catharina G Faber, Nanna B Finnerup, Janne Gierthmühlen, Yelena Granovsky, Sandra Sif Gylfadottir, Harry L Hébert, Troels S Jensen, Jishi John, Harriet I Kemp, Giuseppe Lauria, Helen Laycock, Weihua Meng, Kristian Bernhard Nilsen, Colin Palmer, Andrew S C Rice, Jordi Serra, Blair H Smith, Solomon Tesfaye, Leah Shafran Topaz, Abirami Veluchamy, Jan Vollert, David Yarnitsky, Natalie van Zuydam, John Anker Zwart, Mark I McCarthy, Valeriya Lyssenko, David L Benne |
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