Detalhe da pesquisa
1.
Neuropsychological Profile of an Adolescent Female With Ectodermal Dysplasia With Hypohidrosis.
Cogn Behav Neurol
; 34(3): 212-219, 2021 09 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34473673
2.
Neurofibromatosis Type 1 Implicates Ras Pathways in the Genetic Architecture of Neurodevelopmental Disorders.
Behav Genet
; 50(4): 191-202, 2020 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32026187
3.
An executive functioning perspective in neurofibromatosis type 1: from ADHD and autism spectrum disorder to research domains.
Childs Nerv Syst
; 36(10): 2321-2332, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32617712
4.
Pre- and Perinatal Ischemia-Hypoxia, the Ischemia-Hypoxia Response Pathway, and ADHD Risk.
Behav Genet
; 46(3): 467-77, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-26920003
5.
Association of Multidimensional Schizotypy with PID-5 Domains and Facets.
J Pers Disord
; 36(6): 680-700, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36454161
6.
COMT and anxiety and cognition in children with chromosome 22q11.2 deletion syndrome.
Psychiatry Res
; 178(2): 433-6, 2010 Jul 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-20488547
7.
Evidence of gray matter reduction and dysfunction in chromosome 22q11.2 deletion syndrome.
Psychiatry Res
; 181(1): 1-8, 2010 Jan 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-19962860
8.
Socioeconomic status and psychological function in children with chromosome 22q11.2 deletion syndrome: implications for genetic counseling.
J Genet Couns
; 19(5): 535-44, 2010 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-20680421
9.
Neurological soft signs in psychometrically identified schizotypy.
Schizophr Res
; 115(2-3): 293-302, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19651490