Intelligence and Executive Functions: A Comprehensive Assessment of Intellectually Gifted Children

Autor: A Bucaille, C Jarry, J Allard, A Brosseau-Beauvir, J Ropars, S Brochard, S Peudenier, A Roy

Publikováno v: Archives of Clinical Neuropsychology.

ObjectiveExecutive functions (EFs) play a key role in cognitive and behavioral functioning. Their multiple forms and implications for daily life behaviors mean they are sometimes equated with intelligence. Several elements even suggest that intellect

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::ffbd472131d4ee092be13a0eb8f96b1d
https://doi.org/10.1093/arclin/acad021

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Spinal muscular atrophy with respiratory distress type 1: A multicenter retrospective study

Autor: Maryse Magen, Susana Quijano-Roy, Domitille Gras, Mathilde Nizon, Corinne Magdelaine, Catherine Vanhulle, Fabienne Giuliano, Eric Bieth, Véronique Manel, Damien Haye, Pascal Cintas, Florence Petit, Klaus Dieterich, Agnès Viguier, S. Peudenier, Valérie Lauwers-Cances, Mélanie Fradin, Claude Cances, Isabelle Desguerre, Arnaud Isapof, Michèle Mathieu-Dramard, Michaël Jokic

Publikováno v: Neuromuscular Disorders. 29:114-126

Spinal muscular atrophy with respiratory distress type 1 (SMARD1) is a rare autosomal recessive neuromuscular disorder characterized by progressive motor and respiratory decline during the first year of life. Early and late-onset cases have recently

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f6235cb9dfdca18fb3c4cb2f99a0560
https://doi.org/10.1016/j.nmd.2018.10.002

La douleur chez l’enfant en situation de handicap neurologique : mise au point de la Commission « déficience intellectuelle et handicap » de la Société française de neurologie pédiatrique

Autor: S Peudenier, J Avez-Couturier, D Juzeau, S Joriot

Publikováno v: Archives de Pédiatrie. 25:55-62

Management of pain is one of the major expectations of children with neurological impairment and their families. The medical literature is poor on this topic accounting for approximately 0.15 % of the publications on pain in general. The objective of

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::27947146513717fcf96d929e50b552b8
https://doi.org/10.1016/j.arcped.2017.11.012

A large multicenter study of pediatric myotonic dystrophy type 1 for evidence-based management

Autor: Hubert Journel, Sylvie Ragot-Mandry, Delphine Héron, Brigitte Chabrol, S. Peudenier, Jean-Marie Cuisset, Guillaume Bassez, Pascal Sabouraud, Catherine Sarret, Claude Cances, Mélanie Fradin, Agnès Jacquin-Piques, Julie Perrier-Boeswillald, Isabelle Desguerre, Michèle Mayer, Susana Quijano-Roy, Arnaud Isapof, Vincent Laugel, Marie De Antonio, Frédérique Audic, Nathalie Bach, Emmanuelle Lagrue, C. Espil, Rémi Bellance, Catherine Vanhulle, Armelle Magot, Hervé Testard, Julien Durigneux, Yann Péréon, Cécile Laroche-Raynaud, Romain K. Gherardi, Christine Barnerias, Céline Dogan, Véronique Manel, François Rivier, Dalil Hamroun, Ulrike Walther-Louvier, Christian Richelme

Publikováno v: Neurology
Neurology, American Academy of Neurology, 2019, 92 (8), pp.e852-e865. ⟨10.1212/WNL.0000000000006948⟩
Neurology, 2019, 92 (8), pp.e852-e865. ⟨10.1212/WNL.0000000000006948⟩

ObjectiveTo genotypically and phenotypically characterize a large pediatric myotonic dystrophy type 1 (DM1) cohort to provide a solid frame of data for future evidence-based health management.MethodsAmong the 2,697 patients with genetically confirmed

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::90f5e2b2022b063379e100eade2c6dc6
https://hal.archives-ouvertes.fr/hal-02097112