Detalhe da pesquisa
1.
Whole-genome analysis of human group A rotaviruses in 1980s Japan and evolutionary assessment of global Wa-like strains across half a century.
J Gen Virol
; 105(6)2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38836747
2.
Resurgence of human metapneumovirus infection and influenza after three seasons of inactivity in the post-COVID-19 era in Hokkaido, Japan, 2022-2023.
J Med Virol
; 95(12): e29299, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-38081792
3.
Therapeutic efficacy of intravenous infusion of mesenchymal stem cells in rat perinatal brain injury.
Pediatr Res
; 94(6): 1921-1928, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37422495
4.
Sequence analysis of a feline- and porcine-origin G3P[9] rotavirus A strain in a child with acute gastroenteritis in Japan.
Arch Virol
; 168(2): 45, 2023 Jan 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36609581
5.
An intronic GNAO1 variant leading to in-frame insertion cause movement disorder controlled by deep brain stimulation.
Neurogenetics
; 23(2): 129-135, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35147852
6.
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
7.
Rapidly progressive fatal idiopathic hypertrophic pachymeningitis with brainstem involvement in a child.
Childs Nerv Syst
; 34(9): 1795-1798, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29730790
8.
A combination of genetic and biochemical analyses for the diagnosis of PI3K-AKT-mTOR pathway-associated megalencephaly.
BMC Med Genet
; 18(1): 4, 2017 Jan 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-28086757
9.
Unrecovered synkinesis as a sequela of facial nerve palsy in Kawasaki disease.
Pediatr Int
; 64(1): e14673, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34550631
10.
Transient personality changes with bilateral thalamic infarction in a 12-year-old girl.
Pediatr Int
; 64(1): e15352, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36410724
11.
Subcortical heterotopia appearing as huge midline mass in the newborn brain.
Childs Nerv Syst
; 32(2): 377-80, 2016 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-26231566
12.
Short-term efficacy and safety of rufinamide for Lennox-Gastaut syndrome.
No To Hattatsu
; 48(5): 322-6, 2016 09.
Artigo
em Japonês
| MEDLINE | ID: mdl-30010275
13.
Compound heterozygous GFM2 mutations with Leigh syndrome complicated by arthrogryposis multiplex congenita.
J Hum Genet
; 60(9): 509-13, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26016410
14.
[Importance of measuring blood level of lamotrigine for optimum dosing schedule].
No To Hattatsu
; 46(5): 345-9, 2014 Sep.
Artigo
em Japonês
| MEDLINE | ID: mdl-25403064
15.
Dystonia and Parkinsonism in COA7-related disorders: expanding the phenotypic spectrum.
J Neurol
; 271(1): 419-430, 2024 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-37750949
16.
Changing Patterns of Infectious Diseases Among Hospitalized Children in Hokkaido, Japan, in the Post-COVID-19 Era, July 2019 to June 2022.
Pediatr Infect Dis J
; 42(9): 766-773, 2023 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37257096
17.
Progressive conduction defects and cardiac death in late infantile neuronal ceroid lipofuscinosis.
Dev Med Child Neurol
; 54(7): 663-6, 2012 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22221116
18.
[Effect of neurotropin on chronic headaches in children].
No To Hattatsu
; 44(6): 477-81, 2012 Nov.
Artigo
em Japonês
| MEDLINE | ID: mdl-23240530
19.
A new case of concurrent existence of PRRT2-associated paroxysmal movement disorders with c.649dup variant and 16p11.2 microdeletion syndrome.
Brain Dev
; 44(7): 474-479, 2022 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-35400548
20.
Two novel heterozygous variants in ATP1A3 cause movement disorders.
Hum Genome Var
; 9(1): 7, 2022 Feb 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-35181663