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Richard Delorme

Showing results (201-210 of 225) with videos related to

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Orphanet Journal of Rare Diseases|December 14, 2012
Screening for primary creatine deficiencies in French patients with unexplained neurological symptomsDavid Cheillan, Marie Joncquel-Chevalier Curt, Gilbert Briand, et al.
Molecular Genetics and Metabolism|October 5, 2013
Creatine and guanidinoacetate reference values in a French populationMarie Joncquel-Chevalier Curt, David Cheillan, Gilbert Briand, et al.
Scientific Reports|October 17, 2023
Maternal immune activation during pregnancy is associated with more difficulties in socio-adaptive behaviors in autism spectrum disorderPierre Ellul, Anna Maruani, Valérie Vantalon, et al.
Science Translational Medicine|March 1, 2019
Patients with autism spectrum disorders display reproducible functional connectivity alterationsŠtefan Holiga, Joerg F Hipp, Christopher H Chatham, et al.
European Journal of Human Genetics : EJHG|September 24, 2015
A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disabilityAnne-Laure Mosca-Boidron, Lucie Gueneau, Guillaume Huguet, et al.
NPJ Genomic Medicine|November 5, 2021
A recurrent SHANK3 frameshift variant in Autism Spectrum DisorderLivia O Loureiro, Jennifer L Howe, Miriam S Reuter, et al.
BMJ (Clinical Research Ed.)|November 26, 2025
Benefits and harms of ADHD interventions: umbrella review and platform for shared decision makingCorentin J Gosling, Miguel Garcia-Argibay, Michele De Prisco, et al.
Scientific Data|March 15, 2017
Enhancing studies of the connectome in autism using the autism brain imaging data exchange IIAdriana Di Martino, David O'Connor, Bosi Chen, et al.
BMJ Open|June 4, 2024
European Autism GEnomics Registry (EAGER): protocol for a multicentre cohort study and registryMadeleine Bloomfield, Alexandra Lautarescu, Síofra Heraty, et al.
Plos Genetics|February 21, 2012
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disordersClaire S Leblond, Jutta Heinrich, Richard Delorme, et al.
Pageof 23

Showing results (201-210 of 225) with videos related to

Sort By:
Pageof 23
Orphanet Journal of Rare Diseases|December 14, 2012
Screening for primary creatine deficiencies in French patients with unexplained neurological symptomsDavid Cheillan, Marie Joncquel-Chevalier Curt, Gilbert Briand, et al.
Molecular Genetics and Metabolism|October 5, 2013
Creatine and guanidinoacetate reference values in a French populationMarie Joncquel-Chevalier Curt, David Cheillan, Gilbert Briand, et al.
Scientific Reports|October 17, 2023
Maternal immune activation during pregnancy is associated with more difficulties in socio-adaptive behaviors in autism spectrum disorderPierre Ellul, Anna Maruani, Valérie Vantalon, et al.
Science Translational Medicine|March 1, 2019
Patients with autism spectrum disorders display reproducible functional connectivity alterationsŠtefan Holiga, Joerg F Hipp, Christopher H Chatham, et al.
European Journal of Human Genetics : EJHG|September 24, 2015
A de novo microdeletion of SEMA5A in a boy with autism spectrum disorder and intellectual disabilityAnne-Laure Mosca-Boidron, Lucie Gueneau, Guillaume Huguet, et al.
NPJ Genomic Medicine|November 5, 2021
A recurrent SHANK3 frameshift variant in Autism Spectrum DisorderLivia O Loureiro, Jennifer L Howe, Miriam S Reuter, et al.
BMJ (Clinical Research Ed.)|November 26, 2025
Benefits and harms of ADHD interventions: umbrella review and platform for shared decision makingCorentin J Gosling, Miguel Garcia-Argibay, Michele De Prisco, et al.
Scientific Data|March 15, 2017
Enhancing studies of the connectome in autism using the autism brain imaging data exchange IIAdriana Di Martino, David O'Connor, Bosi Chen, et al.
BMJ Open|June 4, 2024
European Autism GEnomics Registry (EAGER): protocol for a multicentre cohort study and registryMadeleine Bloomfield, Alexandra Lautarescu, Síofra Heraty, et al.
Plos Genetics|February 21, 2012
Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disordersClaire S Leblond, Jutta Heinrich, Richard Delorme, et al.
Pageof 23