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1.
Neuropsychological features in RASopathies: A pilot study on parent training program involving families of children with Noonan syndrome.
Am J Med Genet C Semin Med Genet
; 190(4): 510-519, 2022 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-36490374
2.
Corrigendum: PTCHD1 gene mutation/deletion: the cognitive-behavioral phenotyping of four case reports.
Front Psychiatry
; 15: 1375954, 2024.
Artículo
en Inglés
| MEDLINE | ID: mdl-38414498
3.
"Corp-Osa-Mente", a Combined Psychosocial-Neuropsychological Intervention for Adolescents and Young Adults with Fragile X Syndrome: An Explorative Study.
Brain Sci
; 13(2)2023 Feb 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-36831819
4.
PTCHD1 gene mutation/deletion: the cognitive-behavioral phenotyping of four case reports.
Front Psychiatry
; 14: 1327802, 2023.
Artículo
en Inglés
| MEDLINE | ID: mdl-38288059
5.
Open-Label Sulforaphane Trial in FMR1 Premutation Carriers with Fragile-X-Associated Tremor and Ataxia Syndrome (FXTAS).
Cells
; 12(24)2023 12 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-38132093
6.
Insight and Recommendations for Fragile X-Premutation-Associated Conditions from the Fifth International Conference on FMR1 Premutation.
Cells
; 12(18)2023 09 21.
Artículo
en Inglés
| MEDLINE | ID: mdl-37759552
7.
A Comparison of Adaptive Functioning Between Children With Duplication 7 Syndrome and Williams-Beuren Syndrome: A Pilot Investigation.
Front Psychiatry
; 13: 863909, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-35599769
8.
Differences and Similarities in Adaptive Functioning between Children with Autism Spectrum Disorder and Williams-Beuren Syndrome: A Longitudinal Study.
Genes (Basel)
; 13(7)2022 07 16.
Artículo
en Inglés
| MEDLINE | ID: mdl-35886049
9.
Obsessive Compulsive "Paper Handling": A Potential Distinctive Behavior in Children and Adolescents with KBG Syndrome.
J Clin Med
; 11(16)2022 Aug 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-36012925
10.
Characterization of Cognitive, Language and Adaptive Profiles of Children and Adolescents with Malan Syndrome.
J Clin Med
; 11(14)2022 Jul 14.
Artículo
en Inglés
| MEDLINE | ID: mdl-35887841
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