Detalhe da pesquisa
1.
Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development.
Mol Psychiatry
; 28(4): 1647-1663, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36117209
2.
A cross-sectional investigation of cognition and epileptiform discharges in juvenile absence epilepsy.
Epilepsia
; 64(3): 742-753, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36625418
3.
A randomized controlled trial of remote microphone listening devices to treat auditory deficits in children with neurofibromatosis type 1.
Neurol Sci
; 43(9): 5637-5641, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-35723774
4.
The severe epilepsy syndromes of infancy: A population-based study.
Epilepsia
; 62(2): 358-370, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33475165
5.
Circulating tumor DNA for malignant peripheral nerve sheath tumors in neurofibromatosis type 1.
J Neurooncol
; 154(3): 265-274, 2021 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-34529228
6.
Clinical application of the PedsQL Epilepsy Module (PedsQL-EM) in an ambulatory pediatric epilepsy setting.
Epilepsy Behav
; 106: 107005, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-32199347
7.
Correction: Genetic aetiologies for childhood speech disorder: novel pathways co-expressed during brain development.
Mol Psychiatry
; 28(4): 1664-1666, 2023 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-36658335
8.
Risk of seizures in children with tectal gliomas.
Epilepsia
; 56(9): e139-42, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26193802
9.
Bacillus cereus Cerebral Abscess During Induction Chemotherapy for Childhood Acute Leukemia.
J Pediatr Hematol Oncol
; 37(7): 568-9, 2015 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-26274034
10.
Cost Analysis of Orthoptist-Led Neurofibromatosis Type 1 Screening Clinics.
Br Ir Orthopt J
; 19(1): 26-34, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-37063611
11.
Sex- and age-related differences in autistic behaviours in children with neurofibromatosis type 1.
J Autism Dev Disord
; 53(7): 2835-2850, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-35445370
12.
Acute bilateral myopia caused by lamotrigine-induced uveal effusions.
J Paediatr Child Health
; 53(10): 1013-1014, 2017 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-28636263
13.
Delineating the autistic phenotype in children with neurofibromatosis type 1.
Mol Autism
; 13(1): 3, 2022 01 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34983638
14.
Aberrant splicing and transcriptional activity of TPP1 result in CLN2-like disorder.
Eur J Med Genet
; 64(8): 104259, 2021 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-34126256
15.
Auditory Dysfunction Among Individuals With Neurofibromatosis Type 1.
JAMA Netw Open
; 4(12): e2136842, 2021 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34870681
16.
Contribution of rare genetic variants to drug response in absence epilepsy.
Epilepsy Res
; 170: 106537, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33421703
17.
Nummular headache associated with focal hair heterochromia in a child.
Cephalalgia
; 30(11): 1403-5, 2010 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-20959435
18.
Understanding autism spectrum disorder and social functioning in children with neurofibromatosis type 1: protocol for a cross-sectional multimodal study.
BMJ Open
; 9(9): e030601, 2019 09 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-31558455
19.
Spinal Cord Hyperintensities in Neurofibromatosis Type 1: Are They the Cord Equivalent of Unidentified Bright Objects in the Brain?
Pediatr Neurol
; 86: 63-65, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30174245
20.
Consensus research priorities for paediatric status epilepticus: A Delphi study of health consumers, researchers and clinicians.
Seizure
; 56: 104-109, 2018 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-29471256