Detalhe da pesquisa
1.
Task-independent neural bases of peer presence effect on cognition in children and adults.
Neuroimage
; 277: 120247, 2023 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37385049
2.
Adaptive behavior and psychiatric comorbidities in KCNB1 encephalopathy.
Epilepsy Behav
; 126: 108471, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34915430
3.
Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior.
Genet Med
; 23(6): 1028-1040, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33658631
4.
Erotomania and phenotypic continuum in a family frameshift variant of AUTS2: a case report and review.
BMC Psychiatry
; 21(1): 360, 2021 07 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-34273950
5.
Expanding the genetic and phenotypic relevance of KCNB1 variants in developmental and epileptic encephalopathies: 27 new patients and overview of the literature.
Hum Mutat
; 41(1): 69-80, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31513310
6.
Widening of the genetic and clinical spectrum of Lamb-Shaffer syndrome, a neurodevelopmental disorder due to SOX5 haploinsufficiency.
Genet Med
; 22(3): 524-537, 2020 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-31578471
7.
Chromatin remodeling dysfunction extends the etiological spectrum of schizophrenia: a case report.
BMC Med Genet
; 21(1): 10, 2020 01 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-31914951
8.
Developmental and epilepsy spectrum of KCNB1 encephalopathy with long-term outcome.
Epilepsia
; 61(11): 2461-2473, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32954514
9.
Smith-Magenis Syndrome: Molecular Basis of a Genetic-Driven Melatonin Circadian Secretion Disorder.
Int J Mol Sci
; 20(14)2019 Jul 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-31330985
10.
Computer-based cognitive remediation program for the treatment of behavioral problems in children with intellectual disability: the «COGNITUS & MOI¼ study protocol for a randomized controlled trial.
BMC Psychiatry
; 18(1): 235, 2018 07 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-30029627
11.
Autism spectrum disorder associated with 49,XYYYY: case report and review of the literature.
BMC Med Genet
; 18(1): 9, 2017 Jan 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-28137251
12.
Complex phenotype with social communication disorder caused by mosaic supernumerary ring chromosome 19p.
BMC Med Genet
; 15: 132, 2014 Dec 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-25496186
13.
Evidence for dopaminergic denervation in classical galactosemia.
Mov Disord
; 32(6): 940-942, 2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28370299
14.
Relationships between cognitive functions and driving behavior in Parkinson's disease.
Eur Neurol
; 68(2): 98-107, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22759624
15.
Noradrenaline and Movement Initiation Disorders in Parkinson's Disease: A Pharmacological Functional MRI Study with Clonidine.
Cells
; 11(17)2022 08 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-36078048
16.
The Almirall European Headache Awards 2009.
J Headache Pain
; 11(3): 207-14, 2010 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-20369271
17.
Neural representations of transitive relations predict current and future math calculation skills in children.
Neuropsychologia
; 141: 107410, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32097661
18.
Acute paraplegia due to spinal arteriovenous fistula in two patients with hereditary hemorrhagic telangiectasia.
Eur J Pediatr
; 168(2): 135-9, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19020899
19.
Subthreshold social cognitive deficits may be a key to distinguish 22q11.2DS from schizophrenia.
Early Interv Psychiatry
; 13(2): 304-307, 2019 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-29575660
20.
12q13.12q13.13 microdeletion encompassing ACVRL1 and SCN8A genes: Clinical report of a new contiguous gene syndrome.
Eur J Med Genet
; 62(11): 103565, 2019 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-30389587