Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Disease and ATP1A2[original query] |
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| Thyrotoxic periodic paralysis and polymorphisms of sodium-potassium ATPase genes. Clinical endocrinology 2006 Feb 64 (2): 158-61. Kung Annie W C, Lau K S, Cheung William M W, Chan Vivi |
| Association between sodium- and potassium-activated adenosine triphosphatase alpha isoforms and bipolar disorders. Biological psychiatry 2009 Jun 65 (11): 985-91. Goldstein Inbal, Lerer Elad, Laiba Efrat, Mallet Jacques, Mujaheed Mustafa, Laurent Claudine, Rosen Haim, Ebstein Richard P, Lichtstein Dav |
| Novel and de novo mutations in pediatric refractory epilepsy. Molecular brain 2018 9 11 (1): 48. Liu Jing, Tong Lili, Song Shuangshuang, Niu Yue, Li Jun, Wu Xiu, Zhang Jie, Zai Clement C, Luo Fang, Wu Jian, Li Haiyin, Wong Albert H C, Sun Ruopeng, Liu Fang, Li Baom |
| Familial hemiplegic migraine in pediatric patients: A genetic, clinical, and follow-up study. Headache 2023 6 . Giuseppe Donato Mangano, Maria Rita Capizzi, Elide Mantuano, Liana Veneziano, Giuseppe Santangelo, Giuseppe Quatrosi, Rosaria Nardello, Vincenzo Raie |
| Exploring the association between familial hemiplegic migraine genes (CACNA1A, ATP1A2 and SCN1A) with migraine and epilepsy: A UK Biobank exome-wide association study. Cephalalgia : an international journal of headache 2025 1 45 (1): 3331024241306103. Christian Staehr, Mette Nyegaard, Flemming W Bach, Palle Duun Rohde, Vladimir V Matchk |
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