Detalhe da pesquisa
1.
Investigation of the efficacy and adverse effects of lacosamide over 36 months.
Epilepsy Behav
; 144: 109227, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-37207404
2.
Exploratory analysis of plasma cytokine/chemokine levels in 6-year-old children from a birth cohort study.
Cytokine
; 130: 155051, 2020 Mar 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32151964
3.
Psychometric profile of the Ages and Stages Questionnaires, Japanese translation.
Pediatr Int
; 61(11): 1086-1095, 2019 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-31419360
4.
An Xp22.12 microduplication including RPS6KA3 identified in a family with variably affected intellectual and behavioral disabilities.
J Hum Genet
; 58(11): 755-7, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-23985797
5.
Valine-restricted diet for patients with ECHS1 deficiency: Divergent clinical outcomes in two Japanese siblings.
Brain Dev
; 43(2): 308-313, 2021 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-33139125
6.
Dopaminergic restoration of prefrontal cortico-putaminal network in gene therapy for aromatic l-amino acid decarboxylase deficiency.
Brain Commun
; 3(3): fcab078, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-34423296
7.
Valine metabolites analysis in ECHS1 deficiency.
Mol Genet Metab Rep
; 29: 100809, 2021 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-34667719
8.
Praxis-induced reflex seizures in two Japanese cases with ring chromosome 20 syndrome.
Epileptic Disord
; 22(2): 214-218, 2020 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32301722
9.
MELAS syndrome with m.4450 Gâ¯>â¯A mutation in mitochondrial tRNAMet gene.
Brain Dev
; 41(5): 465-469, 2019 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-30739820
10.
Leigh syndrome with spinal cord involvement due to a hemizygous NDUFA1 mutation.
Brain Dev
; 40(6): 498-502, 2018 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-29506883
11.
Late-onset Leigh syndrome with myoclonic epilepsy with ragged-red fibers.
Brain Dev
; 35(6): 582-5, 2013 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22981260
12.
Expression analysis and mutation detection of DLX5 and DLX6 in autism.
Brain Dev
; 32(2): 98-104, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19195802