首页 > 按专业查询名词 > 查询PubMed相关文献
名词信息
Pubmed相关的文献
benign neonatal convulsion相关文献:
The phenotypic spectrum of SCN2A-related epilepsy.
Reynolds C, King MD, Gorman KM.
Eur J Paediatr Neurol. 2020 Jan;24:117-122. doi: 10.1016/j.ejpn.2019.12.016. Epub 2019 Dec 12.
PMID:31924505
Levetiracetam Versus Phenobarbital for Neonatal Seizures: A Randomized Controlled Trial.
Sharpe C, Reiner GE, Davis SL, Nespeca M, Gold JJ, Rasmussen M, Kuperman R, Harbert MJ, Michelson D, Joe P, Wang S, Rismanchi N, Le NM, Mower A, Kim J, Battin MR, Lane B, Honold J, Knodel E, Arnell K, Bridge R, Lee L, Ernstrom K, Raman R, Haas RH; NEOLEV2 INVESTIGATORS.
Pediatrics. 2020 Jun;145(6):e20193182. doi: 10.1542/peds.2019-3182. Epub 2020 May 8.
PMID:32385134
Neonatal Epileptic Encephalopathies.
Ahmad SF, Ahmad KA, Ng YT.
Semin Pediatr Neurol. 2021 Apr;37:100880. doi: 10.1016/j.spen.2021.100880. Epub 2021 Mar 4.
PMID:33892847
[Benign neonatal convulsion].
Okumura A, Watanabe K.
Ryoikibetsu Shokogun Shirizu. 2002;(37 Pt 6):58-60.
PMID:12483828
Neonatal epilepsy genetics.
Axeen EJT, Olson HE.
Semin Fetal Neonatal Med. 2018 Jun;23(3):197-203. doi: 10.1016/j.siny.2018.01.003. Epub 2018 Jan 31.
PMID:29426807
SCN2A-Related Epilepsy: The Phenotypic Spectrum, Treatment and Prognosis.
Zeng Q, Yang Y, Duan J, Niu X, Chen Y, Wang D, Zhang J, Chen J, Yang X, Li J, Yang Z, Jiang Y, Liao J, Zhang Y.
Front Mol Neurosci. 2022 Mar 30;15:809951. doi: 10.3389/fnmol.2022.809951. eCollection 2022.
PMID:35431799
[Benign familial neonatal convulsion].
Yamagata T.
Ryoikibetsu Shokogun Shirizu. 2002;(37 Pt 6):54-7.
PMID:12483827
The ILAE classification of seizures and the epilepsies: Modification for seizures in the neonate. Position paper by the ILAE Task Force on Neonatal Seizures.
Pressler RM, Cilio MR, Mizrahi EM, Moshé SL, Nunes ML, Plouin P, Vanhatalo S, Yozawitz E, de Vries LS, Puthenveettil Vinayan K, Triki CC, Wilmshurst JM, Yamamoto H, Zuberi SM.
Epilepsia. 2021 Mar;62(3):615-628. doi: 10.1111/epi.16815. Epub 2021 Feb 1.
PMID:33522601
[Convulsion, benign familial neonatal].
Kubota H, Ishikiriyama S.
Ryoikibetsu Shokogun Shirizu. 2001;(33):490-1.
PMID:11462531
Epilepsy Syndromes in the First Year of Life and Usefulness of Genetic Testing for Precision Therapy.
Bayat A, Bayat M, Rubboli G, Møller RS.
Genes (Basel). 2021 Jul 8;12(7):1051. doi: 10.3390/genes12071051.
PMID:34356067
© Copyright 2021 鸿泰茂源  版权所有All Rights Reserved京ICP备11040441号-3