Detalhe da pesquisa
1.
Cognitive phenotype of childhood myotonic dystrophy type 1: A multicenter pooled analysis.
Muscle Nerve
; 68(1): 57-64, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37129457
2.
Use of the experience sampling method in adolescents with Duchenne muscular dystrophy: a feasibility study.
Eur Child Adolesc Psychiatry
; 2023 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37914846
3.
Computerized working memory training in males with Duchenne muscular dystrophy: A single case experimental design study.
Neuropsychol Rehabil
; 33(8): 1325-1348, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-35876193
4.
Correction to: Towards a Better Understanding of Cognitive Deficits in Absence Epilepsy: a Systematic Review and Meta-Analysis.
Neuropsychol Rev
; 30(1): 164-165, 2020 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-31863246
5.
Neurocognitive and behavioural profile in Panayiotopoulos syndrome.
Dev Med Child Neurol
; 62(8): 985-992, 2020 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-32608507
6.
Ketogenic diet for the treatment of pediatric epilepsy: review and meta-analysis.
Childs Nerv Syst
; 36(6): 1099-1109, 2020 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-32173786
7.
De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype.
Am J Hum Genet
; 99(4): 991-999, 2016 Oct 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27693232
8.
Towards a Better Understanding of Cognitive Deficits in Absence Epilepsy: a Systematic Review and Meta-Analysis.
Neuropsychol Rev
; 29(4): 421-449, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31776780
9.
Lower myelin-water content of the frontal lobe in childhood absence epilepsy.
Epilepsia
; 60(8): 1689-1696, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31283841
10.
Instruments for the Assessment of Behavioral and Psychosocial Functioning in Duchenne and Becker Muscular Dystrophy; a Systematic Review of the Literature.
J Pediatr Psychol
; 44(10): 1205-1223, 2019 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31429914
11.
Pneumocephalus: a rare and life-threatening, but reversible, complication after penetrating lumbar injury.
Acta Neurochir (Wien)
; 161(2): 361-365, 2019 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30652201
12.
Accelerated cognitive decline in a rodent model for temporal lobe epilepsy.
Epilepsy Behav
; 65: 33-41, 2016 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-27865173
13.
De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype.
Am J Hum Genet
; 100(1): 179, 2017 01 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28061364
14.
Mutations in KCNT1 cause a spectrum of focal epilepsies.
Epilepsia
; 56(9): e114-20, 2015 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-26122718
15.
Vagus nerve stimulation lead removal or replacement: surgical technique, institutional experience, and literature overview.
Acta Neurochir (Wien)
; 157(11): 1917-24, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26335753
16.
Efficacy of methylphenidate treatment in childhood myotonic dystrophy type 1 and comorbid attention deficit hyperactivity disorder: A case report using eye tracking assessment.
Brain Dev
; 46(2): 118-121, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38007339
17.
Surgical complications of vagus nerve stimulation surgery: A 14-years single-center experience.
Brain Spine
; 4: 102733, 2024.
Artigo
em Inglês
| MEDLINE | ID: mdl-38510607
18.
Impact of gastrointestinal and urological symptoms in children with myotonic dystrophy type 1.
Neuromuscul Disord
; 35: 1-7, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-38184901
19.
Psychopharmaceutical treatment for neurobehavioral problems in Duchenne muscular dystrophy: a descriptive study using real-world data.
Neuromuscul Disord
; 33(7): 619-626, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-37453172
20.
Exploring the core network of the structural covariance network in childhood absence epilepsy.
Heliyon
; 9(12): e22657, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-38107302