Detalhe da pesquisa
1.
Changes in interhemispheric coherence after total corpus callosotomy: a scalp EEG study in children with non-lesional generalized epilepsy.
Childs Nerv Syst
; 2024 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38687362
2.
Genetic and clinical landscape of childhood cerebellar hypoplasia and atrophy.
Genet Med
; 24(12): 2453-2463, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36305856
3.
Prenatal clinical manifestations in individuals with COL4A1/2 variants.
J Med Genet
; 58(8): 505-513, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32732225
4.
TSC2 somatic mosaic mutation, including extra-tumor tissue, may be the developmental cause of solitary subependymal giant cell astrocytoma.
Childs Nerv Syst
; 38(1): 77-83, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34741623
5.
Biallelic KARS pathogenic variants cause an early-onset progressive leukodystrophy.
Brain
; 142(3): 560-573, 2019 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30715177
6.
Three Cases of KCNT1 Mutations: Malignant Migrating Partial Seizures in Infancy with Massive Systemic to Pulmonary Collateral Arteries.
J Pediatr
; 191: 270-274, 2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-28987752
7.
Clinicopathological features of neuroblastic tumors with opsoclonus-myoclonus-ataxia syndrome: Follicular structure predicts a better neurological outcome.
Pathol Int
; 67(10): 503-509, 2017 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-28971571
8.
The effect of sevoflurane on electrocorticographic spike activity in pediatric patients with epilepsy.
Paediatr Anaesth
; 27(4): 409-416, 2017 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-28211120
9.
[A case of West syndrome with a deletion at chromosome 2q24.3-q31.3].
No To Hattatsu
; 49(2): 131-5, 2017 03.
Artigo
em Japonês
| MEDLINE | ID: mdl-30113154
10.
Parents'opinions of the changes in their children's epilepsy treatment during the transition from childhood to adulthood.
No To Hattatsu
; 48(4): 271-6, 2016 Jul.
Artigo
em Japonês
| MEDLINE | ID: mdl-30011141
11.
Detecting copy-number variations in whole-exome sequencing data using the eXome Hidden Markov Model: an 'exome-first' approach.
J Hum Genet
; 60(4): 175-82, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25608832
12.
[A clinical study on high-dose erythropoietin therapy for acute encephalopathy or encephalitis].
No To Hattatsu
; 47(1): 32-6, 2015 Jan.
Artigo
em Japonês
| MEDLINE | ID: mdl-25803909
13.
Epileptic encephalopathy with continuous spikes and waves in the occipito-temporal region during slow-wave sleep in two patients with acquired Kanji dysgraphia.
Epileptic Disord
; 16(4): 540-5, 2014 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-25333864
14.
[Clinical evaluation of six patients with anti-NMDAR encephalitis].
No To Hattatsu
; 46(4): 275-80, 2014 Jul.
Artigo
em Japonês
| MEDLINE | ID: mdl-25154224
15.
Successful Hemispherotomy in a Patient With 22q11.2 Deletion Syndrome Who Had Developmental and Epileptic Encephalopathy With Spike-and-Wave Activation During Sleep.
Cureus
; 16(4): e58424, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38765340
16.
Myoclonus-Dystonia Plus Syndrome With Early-Onset Multiple Cerebral Cavernous Malformation Type 1 and Growth Hormone Deficiency Associated With Novel 7q21.13-q21.3 Deletion: A Pediatric Case Report.
Cureus
; 16(3): e56294, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-38628998
17.
Cilostazol treats transient heart failure caused by ATP1A3 variant-associated polymicrogyria.
Brain Dev
; 46(1): 57-61, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37778966
18.
Abnormal axonal development and severe epileptic phenotype in Dynamin-1 (DNM1) encephalopathy.
Epileptic Disord
; 26(1): 139-143, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38009673
19.
Characteristics of malignant brain tumor-associated epileptic spasms.
Epileptic Disord
; 2024 Jun 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-38888438
20.
Total callosotomy ameliorates epileptic activity and improves cognitive function in a patient with Miller-Dieker syndrome.
Epilepsy Behav Rep
; 26: 100670, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38725538