Detalhe da pesquisa
1.
Protective association of HLA-DPB1*04:01:01 with acute encephalopathy with biphasic seizures and late reduced diffusion identified by HLA imputation.
Genes Immun
; 23(3-4): 123-128, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35422513
2.
Familial acute necrotizing encephalopathy without RANBP2 mutation: Poor outcome.
Pediatr Int
; 58(11): 1215-1218, 2016 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-27882739
3.
Vagus Nerve Stimulation Therapy for Drug-Resistant Epilepsy in Children-A Literature Review.
J Clin Med
; 13(3)2024 Jan 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38337474
4.
Genetic and environmental risk factors of acute infection-triggered encephalopathy.
Front Neurosci
; 17: 1119708, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-36761411
5.
Association of IL6 and IL10 gene promotor polymorphisms with susceptibility to acute necrotizing encephalopathy.
Front Neurosci
; 17: 1231957, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37600000
6.
Association of IL-1B rs16944 Polymorphism With Acute Encephalopathy With Biphasic Seizures and Late Reduced Diffusion Is Opposite to That of Febrile Seizures.
Front Neurol
; 13: 891721, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35707033
7.
GWAS identifies candidate susceptibility loci and microRNA biomarkers for acute encephalopathy with biphasic seizures and late reduced diffusion.
Sci Rep
; 12(1): 1332, 2022 01 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-35079012
8.
Comparison of mortality and survival without major morbidities of very preterm infants with very low birth weight from Japan and Brazil.
Rev Paul Pediatr
; 41: e2021389, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36102406
9.
RANBP2 mutation causing autosomal dominant acute necrotizing encephalopathy attenuates its interaction with COX11.
Neurosci Lett
; 763: 136173, 2021 10 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34400285
10.
Nonconvulsive status epilepticus following rotavirus gastroenteritis in two pediatric patients.
Brain Dev
; 43(9): 958-962, 2021 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-34074562
11.
Recurrent acute necrotizing encephalopathy in a boy with RANBP2 mutation and thermolabile CPT2 variant: The first case of ANE1 in Japan.
Brain Dev
; 43(8): 873-878, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-34059398
12.
Case-control association study of rare nonsynonymous variants of SCN1A and KCNQ2 in acute encephalopathy with biphasic seizures and late reduced diffusion.
J Neurol Sci
; 414: 116808, 2020 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-32276107
13.
Epidemiological changes of acute encephalopathy in Japan based on national surveillance for 2014-2017.
Brain Dev
; 42(7): 508-514, 2020 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-32360071
14.
[Effects of piracetam therapy in a case of Lance-Adams syndrome].
No To Hattatsu
; 41(5): 357-60, 2009 Sep.
Artigo
em Japonês
| MEDLINE | ID: mdl-19764456
15.
Acute necrotizing encephalopathy and a carnitine palmitoyltransferase 2 variant in an adult.
J Clin Neurosci
; 61: 264-266, 2019 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-30470651
16.
Thermolabile polymorphism of carnitine palmitoyltransferase 2: A genetic risk factor of overall acute encephalopathy.
Brain Dev
; 41(10): 862-869, 2019 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-31351739
17.
Comparison of mortality and survival without major morbidities of very preterm infants with very low birth weight from Japan and Brazil / Comparação entre mortalidade e sobrevida sem morbidades importantes dos recém-nascidos prematuros de muito baixo peso entre o Japão e o Brasil
Rev. Paul. Pediatr. (Ed. Port., Online)
; 41: e2021389, 2023. tab, graf
Artigo
em Inglês
|
LILACS-Express
| ID: biblio-1406949
18.
High-dose lorazepam for convulsive status epilepticus in an infant with holoprosencephaly.
Pediatr Int
; 52(4): 664-7, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20958878
19.
Missense mutations in sodium channel SCN1A and SCN2A predispose children to encephalopathy with severe febrile seizures.
Epilepsy Res
; 117: 1-6, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26311622
20.
Mutations in the genes encoding eukaryotic translation initiation factor 2B in Japanese patients with vanishing white matter disease.
Brain Dev
; 37(10): 960-6, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25843247