Human Genome Epidemiology Literature Finder
Records 1 - 5 (of 5 Records) |
Query Trace: Syndrome and CHRNA4[original query] |
---|
Suggestive evidence for association of two potassium channel genes with different idiopathic generalised epilepsy syndromes. Epilepsy research 2002 Dec 52 (2): 107-16. Chioza B, Osei-Lah A, Wilkie H, Nashef L, McCormick D, Asherson P, Makoff A |
Association of the neuronal nicotinic acetylcholine receptor subunit alpha4 polymorphisms with febrile convulsions. Epilepsia 2003 Aug 44 (8): 1089-93. Chou I-Ching, Lee Cheng-Chun, Huang Chao-Ching, Wu Jer-Yuarn, Tsai Jeffrey J P, Tsai Chang-Hai, Tsai Fuu-J |
Effects of APOE and CHRNA4 genotypes on retinal nerve fibre layer thickness at the optic disc and on risk for developing exfoliation syndrome. Acta ophthalmologica Scandinavica 2007 May 85 (3): 257-61. Ritland Jon Ståle, Utheim Tor Paaske, Utheim Oygunn Aass, Espeseth Thomas, Lydersen Stian, Semb Svein Ove, Rootwelt Helge, Elsås T |
The 1674+11C>T polymorphism of CHRNA4 is associated with juvenile myoclonic epilepsy. Seizure 2009 Oct 18 (8): 601-3. Rozycka Agata, Steinborn Barbara, Trzeciak Wieslaw |
Sleep-related hypermotor epilepsy (SHE): Contribution of known genes in 103 patients. Seizure 2019 12 74 60-64. Licchetta Laura, Pippucci Tommaso, Baldassari Sara, Minardi Raffaella, Provini Federica, Mostacci Barbara, Plazzi Giuseppe, Tinuper Paolo, Bisulli Francesca, |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: