Remediation of Allophonic Perception and Visual Attention Span in Developmental Dyslexia: A Joint Assay

Autor: Rachel Zoubrinetzky, Gregory Collet, Marie-Ange Nguyen-Morel, Sylviane Valdois, Willy Serniclaes

Publikováno v: Frontiers in Psychology, Vol 10 (2019)

Categorical perception of phonemes and visual attention span are cognitive processes that contribute independently to poor reading skills in developmental dyslexia. We here explored whether training programs specifically targeting one or the other pr

Externí odkaz: https://doaj.org/article/8fa267113bc6477d8d87d6465ec5fdf4

Correction: The phenotypic spectrum of WWOX-related disorders: 20 additional cases of WOREE syndrome and review of the literature

Autor: Marie-Christine Nougues, Ddd Study, Yoshimi Sogawa, Juliette Piard, Christophe Philippe, John Taylor, Delphine Héron, Jenny C. Taylor, Romina Romaniello, Mathieu Milh, Pradeep Vasudevan, Oana Tarta Arsene, Usha Kini, Tiffany Busa, Debbie Shears, Mélanie Fradin, Diana Johnson, Yline Capri, Lara Hawkes, Myrthe van den Born, Gabriela E. Jones, Elise Brischoux-Boucher, Alistair T. Pagnamenta, Agathe Roubertie, Cyril Mignot, Helen V. Firth, Caroline Nava, Laurent Villard, Renato Borgatti, Marie-Ange Nguyen-Morel, Michel Koenig

Publikováno v: Genetics in Medicine. 21:1-5

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::81a886d73202ef84ad1a0906b6491668
https://doi.org/10.1038/s41436-019-0460-y

CACNA1A-associated epilepsy: Electroclinical findings and treatment response on seizures in 18 patients

Autor: Magalie Barth, Marie-Ange Nguyen-Morel, Marie Le Roux, Florence Renaldo, Nathalie Villeneuve, Florence Riant, Alec Aeby, Lionel Arnaud, Arnaud Biraben, Claude Cances, Catheline Vilain, Anne-Isabelle Vermersch, Patrick Van Bogaert, Edouard Hirsch, Chloé Angelini, Laurence Chaton, Gaetan Lesca, Julien Van Gils, Laurent Villard, Sophie Gueden, Patrick Desbordes de Cepoy, Vincent des Portes, Luc Valton, Cecilia Altuzarra, Audrey Riquet, Anne de Saint Martin

Publikováno v: European Journal of Paediatric Neurology
European Journal of Paediatric Neurology, 2021, 33, pp.75-85. ⟨10.1016/j.ejpn.2021.05.010⟩
European Journal of Paediatric Neurology, Elsevier, 2021, 33, pp.75-85. ⟨10.1016/j.ejpn.2021.05.010⟩

International audience; CACNA1A pathogenic mutations are involved in various neurological phenotypes including episodic ataxia (EA2), spinocerebellar ataxia (SCA6), and familial hemiplegic migraine (FHM1). Epilepsy is poorly documented. We studied 18

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc4496805228d3d29deb659a147f2ff8
https://pubmed.ncbi.nlm.nih.gov/34102571

Phonological skills, visual attention span, and visual stress in developmental dyslexia

Autor: Franck Ramus, Marie-Ange Nguyen-Morel, Yves Chaix, Florence George, Laure Bricout, Stéphanie Iannuzzi, Isabelle Soares-Boucaud, Catherine Billard, Amanda Saksida, Jean-François Démonet, Marie-France Le Heuzey, Caroline Bogliotti, Johannes C. Ziegler

Publikováno v: Developmental Psychology
Developmental Psychology, 2016, 52 (10), pp.1503-1516. ⟨10.1037/dev0000184⟩
Developmental Psychology, American Psychological Association, 2016, 52 (10), pp.1503-1516. ⟨10.1037/dev0000184⟩

In this study, we concurrently investigated 3 possible causes of dyslexia-a phonological deficit, visual stress, and a reduced visual attention span-in a large population of 164 dyslexic and 118 control French children, aged between 8 and 13 years ol

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d3082bdee11f0d48aa7912d50abf06b
https://hal.science/hal-01400569

A Thermolabile Aldolase A Mutant Causes Fever-Induced Recurrent Rhabdomyolysis without Hemolytic Anemia

Autor: Valérie Serre, Monique Piraud, Norma B. Romero, Florence Habarou, Asmaa Mamoune, Jean-Laurent Casanova, Michele Pelosi, Pascale de Lonlay, Mai Thao Viou, Patrick Nusbaum, Luc Nonnenmacher, Marie-Ange Nguyen Morel, Yamina Hamel, Chris Ottolenghi, Bertrand Boisson, Michel Bahuau, Sabrina Vergnaud, Joseph Vamecq

Publikováno v: PLoS Genetics
PLoS Genetics, 2014, 10 (11), pp.e1004711. ⟨10.1371/journal.pgen.1004711⟩
PLoS Genetics, Public Library of Science, 2014, 10 (11), pp.e1004711. ⟨10.1371/journal.pgen.1004711⟩
PLoS Genetics, Vol 10, Iss 11, p e1004711 (2014)
PLoS Genetics, Public Library of Science, 2014, 10 (11), pp.e1004711. <10.1371/journal.pgen.1004711>
PLoS Genetics, Public Library of Science, 2014, 10 (11), pp.e1004711. 〈10.1371/journal.pgen.1004711〉

International audience; Aldolase A deficiency has been reported as a rare cause of hemolytic anemia occasionally associated with myopathy. We identified a deleterious homozygous mutation in the ALDOA gene in 3 siblings with episodic rhabdomyolysis wi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f5c8db83b83ef06965344b833450846
https://hal.sorbonne-universite.fr/hal-01342663