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Page 1
Exome Sequencing and the Identification of New Genes and Shared Mechanisms in Polymicrogyria.
Akula SK, Chen AY, Neil JE, Shao DD, Mo A, Hylton NK, DiTroia S, Ganesh VS, Smith RS, O'Kane K, Yeh RC, Marciano JH, Kirkham S, Kenny CJ, Song JHT, Al Saffar M, Millan F, Harris DJ, Murphy AV, Klemp KC, Braddock SR, Brand H, Wong I, Talkowski ME, O'Donnell-Luria A, Lai A, Hill RS, Mochida GH, Doan RN, Barkovich AJ, Yang E, Amrom D, Andermann E, Poduri A, Walsh CA; Polymicrogyria Genetics Research Network. Akula SK, et al. JAMA Neurol. 2023 Sep 1;80(9):980-988. doi: 10.1001/jamaneurol.2023.2363. JAMA Neurol. 2023. PMID: 37486637 Free PMC article.
[Lafora disease presentation, two cases in a Mexican family].
González-De la Rosa MG, Alva-Moncayo E. González-De la Rosa MG, et al. Among authors: alva moncayo e. Rev Med Inst Mex Seguro Soc. 2017 Mar-Apr;55(2):252-256. Rev Med Inst Mex Seguro Soc. 2017. PMID: 28296376 Spanish.
[The epileptic syndromes in childhood].
Alva-Moncayo E. Alva-Moncayo E. Rev Med Inst Mex Seguro Soc. 2011 Jan-Feb;49(1):37-44. Rev Med Inst Mex Seguro Soc. 2011. PMID: 21513659 Spanish.
[Quality of life of the pediatric epileptic patient].
Alva-Moncayo E, Cortés-Ríos MP, Juárez-Granados F. Alva-Moncayo E, et al. Rev Neurol. 1998 Jun;26(154):1069-70. Rev Neurol. 1998. PMID: 9658495 Spanish. No abstract available.