Detalhe da pesquisa
1.
Itpr1 regulates the formation of anterior eye segment tissues derived from neural crest cells.
Development
; 148(16)2021 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-34338282
2.
Involvement of brain structures in childhood epilepsy with centrotemporal spikes.
Pediatr Int
; 64(1): e15001, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34562291
3.
[New Attempt of Radiation Oncology Section to Radiotherapy for Head and Neck Cancer].
Gan To Kagaku Ryoho
; 49(9): 981-983, 2022 Sep.
Artigo
em Japonês
| MEDLINE | ID: mdl-36156019
4.
Severe neurocognitive and growth disorders due to variation in THOC2, an essential component of nuclear mRNA export machinery.
Hum Mutat
; 39(8): 1126-1138, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-29851191
5.
Cytotoxic edema at onset in West syndrome of unknown etiology: A longitudinal diffusion tensor imaging study.
Epilepsia
; 59(2): 440-448, 2018 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-29315514
6.
Pathogenic Role of Human Herpesvirus 6B Infection in Mesial Temporal Lobe Epilepsy.
J Infect Dis
; 212(7): 1014-21, 2015 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25840441
7.
Seizure characteristics of epilepsy in childhood after acute encephalopathy with biphasic seizures and late reduced diffusion.
Epilepsia
; 56(8): 1286-93, 2015 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-26118313
8.
The spectrum of ZEB2 mutations causing the Mowat-Wilson syndrome in Japanese populations.
Am J Med Genet A
; 164A(8): 1899-908, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24715670
9.
Social difficulties and care burden of adult Duchenne muscular dystrophy in Japan: a questionnaire survey based on the Japanese Registry of Muscular Dystrophy (Remudy).
Orphanet J Rare Dis
; 19(1): 182, 2024 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38689355
10.
Discrepancy between Clinician-rated and Self-reported Depression Severity is Associated with Adverse Childhood Experience, Autistic-like Traits, and Coping Styles in Mood Disorders.
Clin Psychopharmacol Neurosci
; 21(2): 296-303, 2023 May 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-37119222
11.
Association of Scalp High-Frequency Oscillation Detection and Characteristics With Disease Activity in Pediatric Epilepsy.
J Clin Neurophysiol
; 2023 Oct 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-37934062
12.
Pathological gait in Rett syndrome: Quantitative evaluation using three-dimensional gait analysis.
Eur J Paediatr Neurol
; 42: 15-21, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36493671
13.
Brain Abnormalities in Becker Muscular Dystrophy: Evaluation by Voxel-Based DTI and Morphometric Analysis.
AJNR Am J Neuroradiol
; 44(12): 1405-1410, 2023 12 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37945525
14.
Association between cerebrospinal fluid parameters and developmental and neurological status in glucose transporter 1 deficiency syndrome.
J Neurol Sci
; 447: 120597, 2023 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-36965413
15.
Frontal lobe-dominant cerebral blood flow reduction and atrophy can be progressive in Duchenne muscular dystrophy.
Neuromuscul Disord
; 32(6): 477-485, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35396091
16.
A case of 46,XY disorders of sex development with congenital heart disease caused by a GATA4 variant.
Congenit Anom (Kyoto)
; 62(5): 203-207, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35751412
17.
Early immunological responses to the mRNA SARS-CoV-2 vaccine in patients with neuromuscular disorders.
Front Immunol
; 13: 996134, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36248823
18.
Whole-exome analysis of 177 pediatric patients with undiagnosed diseases.
Sci Rep
; 12(1): 14589, 2022 08 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-36028527
19.
Establishment of in-hospital clinical network for patients with neurofibromatosis type 1 in Nagoya University Hospital.
Sci Rep
; 11(1): 11933, 2021 06 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34099792
20.
Hippocampal Atrophy in Pediatric Transplant Recipients with Human Herpesvirus 6B.
Microorganisms
; 9(4)2021 Apr 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33917715