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Orphanet Journal of Rare Diseases
|
September 5, 2015
Behavioral disturbance and treatment strategies in Smith-Magenis syndrome
Alice Poisson, Alain Nicolas, Pierre Cochat, et al.
Disability and Rehabilitation
|
August 12, 2014
Cognitive remediation therapy (CRT) benefits more to patients with schizophrenia with low initial memory performances
Benoit Pillet, Yannick Morvan, Aurelia Todd, et al.
European Journal of Medical Genetics
|
November 4, 2018
12q13.12q13.13 microdeletion encompassing ACVRL1 and SCN8A genes: Clinical report of a new contiguous gene syndrome
Alice Poisson, Gaetan Lesca, Nicolas Chatron, et al.
American Journal of Medical Genetics. Part A
|
June 10, 2017
Clinical and molecular cytogenetic characterization of four unrelated patients carrying 2p14 microdeletions
Marie-Laure Mathieu, Caroline Demily, Sandra Chantot-Bastaraud, et al.
Psychiatric Genetics
|
April 2, 2019
Corpus callosum metrics predict severity of visuospatial and neuromotor dysfunctions in ARID1B mutations with Coffin-Siris syndrome
Caroline Demily, Charlyne Duwime, Clémence Lopez, et al.
Medecine Sciences : M/S
|
December 18, 2019
[Twenty years of on-site clinical genetics consultations for people with ASD]
Arnold Munnich, Caroline Demily, Lisa Frugère, et al.
International Journal of Environmental Research and Public Health
|
October 14, 2022
Actionable Predictive Factors of Homelessness in a Psychiatric Population: Results from the REHABase Cohort Using a Machine Learning Approach
Guillaume Lio, Malek Ghazzai, Frédéric Haesebaert, et al.
Psychiatric Services (Washington, D.C.)
|
January 30, 2019
Satisfaction and Needs in Serious Mental Illness and Autism Spectrum Disorder: The REHABase Psychosocial Rehabilitation Project
Nicolas Franck, Laura Bon, Marie Dekerle, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 11, 2026
Circulating levels of ghrelin and hyperphagia in patients with rare genetic neurodevelopmental disorders
Gwenaëlle Diene, Grégoire Benvegnu, Cathy Brochado, et al.
Orphanet Journal of Rare Diseases
|
June 2, 2019
Molecular investigation, using chromosomal microarray and whole exome sequencing, of six patients affected by Williams Beuren syndrome and Autism Spectrum Disorder
Julie Masson, Caroline Demily, Nicolas Chatron, et al.
Page
of 8
Search research articles
Search
Showing results (61-70 of 80) with videos related to
Sort By:
Page
of 8
Orphanet Journal of Rare Diseases
|
September 5, 2015
Behavioral disturbance and treatment strategies in Smith-Magenis syndrome
Alice Poisson, Alain Nicolas, Pierre Cochat, et al.
Disability and Rehabilitation
|
August 12, 2014
Cognitive remediation therapy (CRT) benefits more to patients with schizophrenia with low initial memory performances
Benoit Pillet, Yannick Morvan, Aurelia Todd, et al.
European Journal of Medical Genetics
|
November 4, 2018
12q13.12q13.13 microdeletion encompassing ACVRL1 and SCN8A genes: Clinical report of a new contiguous gene syndrome
Alice Poisson, Gaetan Lesca, Nicolas Chatron, et al.
American Journal of Medical Genetics. Part A
|
June 10, 2017
Clinical and molecular cytogenetic characterization of four unrelated patients carrying 2p14 microdeletions
Marie-Laure Mathieu, Caroline Demily, Sandra Chantot-Bastaraud, et al.
Psychiatric Genetics
|
April 2, 2019
Corpus callosum metrics predict severity of visuospatial and neuromotor dysfunctions in ARID1B mutations with Coffin-Siris syndrome
Caroline Demily, Charlyne Duwime, Clémence Lopez, et al.
Medecine Sciences : M/S
|
December 18, 2019
[Twenty years of on-site clinical genetics consultations for people with ASD]
Arnold Munnich, Caroline Demily, Lisa Frugère, et al.
International Journal of Environmental Research and Public Health
|
October 14, 2022
Actionable Predictive Factors of Homelessness in a Psychiatric Population: Results from the REHABase Cohort Using a Machine Learning Approach
Guillaume Lio, Malek Ghazzai, Frédéric Haesebaert, et al.
Psychiatric Services (Washington, D.C.)
|
January 30, 2019
Satisfaction and Needs in Serious Mental Illness and Autism Spectrum Disorder: The REHABase Psychosocial Rehabilitation Project
Nicolas Franck, Laura Bon, Marie Dekerle, et al.
The Journal of Clinical Endocrinology and Metabolism
|
March 11, 2026
Circulating levels of ghrelin and hyperphagia in patients with rare genetic neurodevelopmental disorders
Gwenaëlle Diene, Grégoire Benvegnu, Cathy Brochado, et al.
Orphanet Journal of Rare Diseases
|
June 2, 2019
Molecular investigation, using chromosomal microarray and whole exome sequencing, of six patients affected by Williams Beuren syndrome and Autism Spectrum Disorder
Julie Masson, Caroline Demily, Nicolas Chatron, et al.
Page
of 8