Detalhe da pesquisa
1.
Efficacy of vagus nerve stimulation in 95 children of drug-resistant epilepsy with structural etiology.
Epilepsy Behav
; 140: 109107, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36758359
2.
Genetic analysis of 20 patients with hypomyelinating leukodystrophy by trio-based whole-exome sequencing.
J Hum Genet
; 66(8): 761-768, 2021 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-33597727
3.
Somatic variants in new candidate genes identified in focal cortical dysplasia type II.
Epilepsia
; 61(4): 667-678, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32216069
4.
Upregulation of HMGB1-TLR4 inflammatory pathway in focal cortical dysplasia type II.
J Neuroinflammation
; 15(1): 27, 2018 Jan 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-29382328
5.
[Surgery for pediatric intractable epilepsy due to posterior quadrantic cortical dysplasia].
Zhongguo Dang Dai Er Ke Za Zhi
; 19(3): 259-263, 2017 Mar.
Artigo
em Zh
| MEDLINE | ID: mdl-28302192
6.
Fragile X syndrome screening in Chinese children with unknown intellectual developmental disorder.
BMC Pediatr
; 15: 77, 2015 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26174701
7.
[Clinical presentations of pediatric anti-N-methyl-D-aspartate receptor encephalitis].
Zhongguo Dang Dai Er Ke Za Zhi
; 16(6): 575-7, 2014 Jun.
Artigo
em Zh
| MEDLINE | ID: mdl-24927430
8.
Long-term seizure and developmental outcomes of epilepsy surgery in children under 3 years old: A single-center study of 113 patients.
CNS Neurosci Ther
; 30(1): e14481, 2024 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37786975
9.
[Peripheral nervous impairment in a patient with methylmalonic aciduria combined with hyperhomocysteinemia].
Beijing Da Xue Xue Bao Yi Xue Ban
; 45(2): 303-6, 2013 Apr 18.
Artigo
em Zh
| MEDLINE | ID: mdl-23591356
10.
[Epidemiological study on developmental delay of 18-month-old children from four districts/counties in Beijing].
Beijing Da Xue Xue Bao Yi Xue Ban
; 45(2): 211-6, 2013 Apr 18.
Artigo
em Zh
| MEDLINE | ID: mdl-23591339
11.
Brain functional connectivity-based prediction of vagus nerve stimulation efficacy in pediatric pharmacoresistant epilepsy.
CNS Neurosci Ther
; 29(11): 3259-3268, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37170486
12.
Novel STAMBP mutations in a Chinese girl with rare symptoms of microcephaly-capillary malformation syndrome and Mowat-Wilson syndrome.
Heliyon
; 9(12): e22989, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-38058451
13.
Identiï¬cation of GJC2 gene mutations in Chinese patients with Pelizaeus-Merzbacher-like disease.
Minerva Pediatr (Torino)
; 75(1): 32-38, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-27057822
14.
Efficient and generalizable cross-patient epileptic seizure detection through a spiking neural network.
Front Neurosci
; 17: 1303564, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38268711
15.
Safety and efficacy of rapid withdrawal of antiseizure medications during long-term video-electroencephalogram monitoring in children with drug-resistant epilepsy: A retrospective study.
Epilepsia Open
; 8(2): 313-319, 2023 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-36650667
16.
Pediatric epilepsy surgery in patients with Lennox-Gastaut syndrome after viral encephalitis.
Front Neurol
; 14: 1097535, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36908602
17.
Identification of gene mutations in six Chinese patients with maple syrup urine disease.
Front Genet
; 14: 1132364, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36911408
18.
Clinical characteristics and surgical outcomes in children with mild malformation of cortical development and oligodendroglial hyperplasia in epilepsy.
Epilepsia Open
; 8(3): 898-911, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37144544
19.
NIPA2 located in 15q11.2 is mutated in patients with childhood absence epilepsy.
Hum Genet
; 131(7): 1217-24, 2012 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22367439
20.
Different Mutations of Gap Junction Connexin 47 Lead to Discrepant Activation of Unfolded Protein Response Pathway in Pelizaeus-Merzbacher-Like Disease.
Neuropediatrics
; 48(6): 426-431, 2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-28712094