Human Genome Epidemiology Literature Finder
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Records 1 - 8 (of 8 Records) |
| Query Trace: Disease and ATP1A3[original query] |
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| 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 |
| ATP1A3 mutations and genotype-phenotype correlation of alternating hemiplegia of childhood in Chinese patients. PloS one 2014 9 (5): e97274. Yang Xiaoling, Gao Hua, Zhang Jie, Xu Xiaojing, Liu Xiaoyan, Wu Xiru, Wei Liping, Zhang Yueh |
| Rare Copy Number Variations and Predictors in Children With Intellectual Disability and Epilepsy. Frontiers in neurology 2018 12 9 947. Kessi Miriam, Xiong Juan, Wu Liwen, Yang Lifen, He Fang, Chen Chen, Pang Nan, Duan Haolin, Zhang Wen, Arafat Ahmed, Yin Fei, Peng Ji |
| Delineation of molecular findings by whole-exome sequencing for suspected cases of paediatric-onset mitochondrial diseases in the Southern Chinese population. Human genomics 2020 Sep 14 (1): 28. Tsang Mandy H Y, Kwong Anna K Y, Chan Kate L S, Fung Jasmine L F, Yu Mullin H C, Mak Christopher C Y, Yeung Kit-San, Rodenburg Richard J T, Smeitink Jan A M, Chan Rachel, Tsoi Thomas, Hui Joannie, Wong Shelia S N, Tai Shuk-Mui, Chan Victor C M, Ma Che-Kwan, Fung Sharon T H, Wu Shun-Ping, Chak W K, Chung Brian H Y, Fung Cheuk-Wi |
| 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 |
| Auditory Neuropathy as the Initial Phenotype for Patients With ATP1A3 c.2452 G > A: Genotype-Phenotype Study and CI Management. Frontiers in cell and developmental biology 2021 10 9 749484. Wang Wenjia, Li Jin, Lan Lan, Xie Linyi, Xiong Fen, Guan Jing, Wang Hongyang, Wang Qiu |
| Brain structural changes in alternating hemiplegia of childhood using single-case voxel-based morphometry analysis. International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience 2023 8 . Elly Arizono, Noriko Sato, Yoko Shigemoto, Yukio Kimura, Emiko Chiba, Hiroyuki Maki, Hiroshi Matsuda, Eri Takeshita, Yuko Shimizu-Motohashi, Masayuki Sasaki, Kazuhiro Sai |
| Parkinson's Disease Gene Screening in Familial Cases from Central and South America. Movement disorders : official journal of the Movement Disorder Society 2024 7 . Oswaldo Lorenzo-Betancor, Seysha Mehta, Janvi Ramchandra, Sekinat Mumuney, Artur F Schumacher-Schuh, Mario Cornejo-Olivas, Elison H Sarapura-Castro, Luis Torres, Miguel A Inca-Martinez, Pilar Mazzetti, Carlos Cosentino, Federico Micheli, Vitor Tumas, Elena Dieguez, Victor Raggio, Vanderci Borges, Henrique B Ferraz, Pedro Chana-Cuevas, Marlene Jimenez-Del-Rio, Carlos Velez-Pardo, Sonia Moreno, Francisco Lopera, Jorge L Orozco-Velez, Beatriz Muñoz-Ospina, Carlos R M Rieder, Alex Medina-Escobar, Dora Yearout, Cyrus P Zabetian, Ignacio F Mata, |
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