Detalhe da pesquisa
1.
Understanding neurodevelopmental trajectories and behavioral profiles in SCN1A-related epilepsy syndromes.
Epilepsy Behav
; 154: 109726, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38513571
2.
Exploring individual parent-to-parent support interventions for parents caring for children with brain-based developmental disabilities: A scoping review.
Child Care Health Dev
; 50(3): e13255, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38587275
3.
Psychiatric and neurological manifestations in adults with Smith-Magenis syndrome: A scoping review.
Am J Med Genet B Neuropsychiatr Genet
; 195(2): e32956, 2024 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-37584268
4.
Challenging behavior in children and adolescents with Dravet syndrome: Exploring the lived experiences of parents.
Epilepsy Behav
; 138: 108978, 2023 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36495797
5.
Novel Insights into Somatic Comorbidities in Children and Adolescents Across Psychiatric Diagnoses: An Explorative Study.
Child Psychiatry Hum Dev
; 2023 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37656290
6.
Atypical chromosome 22q11.2 deletions are complex rearrangements and have different mechanistic origins.
Hum Mol Genet
; 28(22): 3724-3733, 2019 11 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-31884517
7.
Neurodevelopmental Trajectories and Psychiatric Morbidity: Lessons Learned From the 22q11.2 Deletion Syndrome.
Curr Psychiatry Rep
; 23(3): 13, 2021 02 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-33625600
8.
Study protocol of a randomized, double-blind, placebo-controlled, multi-center trial to treat antipsychotic-induced weight gain: the Metformin-Lifestyle in antipsychotic users (MELIA) trial.
BMC Psychiatry
; 21(1): 4, 2021 01 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33402159
9.
Psychiatric phenotypes associated with hyperprolinemia: A systematic review.
Am J Med Genet B Neuropsychiatr Genet
; 186(5): 289-317, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34302426
10.
Adverse effects of antipsychotic medication in patients with 22q11.2 deletion syndrome: A systematic review.
Am J Med Genet A
; 179(11): 2292-2306, 2019 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-31407842
11.
The ethics of polygenic scores in psychiatry: minefield or opportunity for patient-centered psychiatry?
Psychiatr Genet
; 34(2): 31-36, 2024 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38441147
12.
Intellectual and Behavioral Phenotypes of Smith-Magenis Syndrome: Comparisons between Individuals with a 17p11.2 Deletion and Pathogenic RAI1 Variant.
Genes (Basel)
; 14(8)2023 07 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-37628566
13.
Parkinsonism in Genetic Neurodevelopmental Disorders: A Systematic Review.
Mov Disord Clin Pract
; 10(1): 17-31, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36699000
14.
Vitamin D status in children with a psychiatric diagnosis, autism spectrum disorders, or internalizing disorders.
Front Psychiatry
; 13: 958556, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36186854
15.
Barriers to genetic testing in clinical psychiatry and ways to overcome them: from clinicians' attitudes to sociocultural differences between patients across the globe.
Transl Psychiatry
; 12(1): 442, 2022 10 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36220808
16.
A qualitative and quantitative study of self-reported positive characteristics of individuals with ADHD.
Front Psychiatry
; 13: 922788, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-36311492
17.
Untargeted metabolic analysis in dried blood spots reveals metabolic signature in 22q11.2 deletion syndrome.
Transl Psychiatry
; 12(1): 97, 2022 03 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35264571
18.
Adults with autism spectrum disorder and the criminal justice system: An investigation of prevalence of contact with the criminal justice system, risk factors and sex differences in a specialist assessment service.
Autism
; 26(8): 2098-2107, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35261275
19.
A normative chart for cognitive development in a genetically selected population.
Neuropsychopharmacology
; 47(7): 1379-1386, 2022 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33782512
20.
COMT Val(158) met genotype and striatal D(2/3) receptor binding in adults with 22q11 deletion syndrome.
Synapse
; 65(9): 967-70, 2011 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21465565