Search details
1.
Prevalence of mental disorders in closed educational centers in France.
Encephale
; 2024 Feb 16.
Article
in English
| MEDLINE | ID: mdl-38368185
2.
[The attachment formed in addictive behaviors during the adolescent process]. / L'attachement noué dans les conduites addictives lors du processus adolescent.
Soins Psychiatr
; 43(342): 27-30, 2022.
Article
in French
| MEDLINE | ID: mdl-36522029
3.
[Research on adolescent depression associated with parental depression]. / Une recherche sur la dépression de l'adolescent associée à la dépression parentale.
Soins Psychiatr
; 43(342): 14-17, 2022.
Article
in French
| MEDLINE | ID: mdl-36522026
4.
Deep phenotyping, including quantitative ciliary beating parameters, and extensive genotyping in primary ciliary dyskinesia.
J Med Genet
; 57(4): 237-244, 2020 04.
Article
in English
| MEDLINE | ID: mdl-31772028
5.
Contribution of functionally assessed GHRHR mutations to idiopathic isolated growth hormone deficiency in patients without GH1 mutations.
Hum Mutat
; 40(11): 2033-2043, 2019 11.
Article
in English
| MEDLINE | ID: mdl-31231873
6.
Mutations in DNAJB13, Encoding an HSP40 Family Member, Cause Primary Ciliary Dyskinesia and Male Infertility.
Am J Hum Genet
; 99(2): 489-500, 2016 08 04.
Article
in English
| MEDLINE | ID: mdl-27486783
7.
RSPH3 Mutations Cause Primary Ciliary Dyskinesia with Central-Complex Defects and a Near Absence of Radial Spokes.
Am J Hum Genet
; 97(1): 153-62, 2015 Jul 02.
Article
in English
| MEDLINE | ID: mdl-26073779
8.
Mutations in GAS8, a Gene Encoding a Nexin-Dynein Regulatory Complex Subunit, Cause Primary Ciliary Dyskinesia with Axonemal Disorganization.
Hum Mutat
; 37(8): 776-85, 2016 08.
Article
in English
| MEDLINE | ID: mdl-27120127
9.
Loss-of-function mutations in RSPH1 cause primary ciliary dyskinesia with central-complex and radial-spoke defects.
Am J Hum Genet
; 93(3): 561-70, 2013 Sep 05.
Article
in English
| MEDLINE | ID: mdl-23993197
10.
Molecular screening of a large cohort of Moroccan patients with congenital hypopituitarism.
Clin Endocrinol (Oxf)
; 82(6): 876-84, 2015 Jun.
Article
in English
| MEDLINE | ID: mdl-25557026
11.
Association between Hpa Axis Functioning and Mental Health in Maltreated Children and Adolescents: A Systematic Literature Review.
Children (Basel)
; 10(8)2023 Aug 03.
Article
in English
| MEDLINE | ID: mdl-37628343
12.
Self/other distinction in adolescents with autism spectrum disorder (ASD) assessed with a double mirror paradigm.
PLoS One
; 18(3): e0275018, 2023.
Article
in English
| MEDLINE | ID: mdl-36928493
13.
Psychosis Caused by a Somatic Condition: How to Make the Diagnosis? A Systematic Literature Review.
Children (Basel)
; 10(9)2023 Aug 23.
Article
in English
| MEDLINE | ID: mdl-37761400
14.
Sympathy-Empathy and the Radicalization of Young People.
Children (Basel)
; 9(12)2022 Dec 02.
Article
in English
| MEDLINE | ID: mdl-36553332
15.
Early Motor Skills in Children With Autism Spectrum Disorders Are Marked by Less Frequent Hand and Knees Crawling.
Percept Mot Skills
; 128(5): 2148-2165, 2021 Oct.
Article
in English
| MEDLINE | ID: mdl-34372738
16.
Deletions at the SOX10 gene locus cause Waardenburg syndrome types 2 and 4.
Am J Hum Genet
; 81(6): 1169-85, 2007 Dec.
Article
in English
| MEDLINE | ID: mdl-17999358
17.
Exploring Self-Consciousness From Self- and Other-Image Recognition in the Mirror: Concepts and Evaluation.
Front Psychol
; 10: 719, 2019.
Article
in English
| MEDLINE | ID: mdl-31133909
18.
Molecular cytogenetic characterization of terminal 14q32 deletions in two children with an abnormal phenotype and corpus callosum hypoplasia.
Eur J Hum Genet
; 16(6): 680-7, 2008 Jun.
Article
in English
| MEDLINE | ID: mdl-18197200
19.
ZFHX1B mutations in patients with Mowat-Wilson syndrome.
Hum Mutat
; 28(4): 313-21, 2007 Apr.
Article
in English
| MEDLINE | ID: mdl-17203459
20.
Recurrent Intragenic Duplication within the NR5A1 Gene and Severe Proximal Hypospadias.
Sex Dev
; 11(5-6): 293-297, 2017.
Article
in English
| MEDLINE | ID: mdl-29332064