Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Emeline Peyric"'
Autor:
Pierre-Yves Postic, Yann Leprince, Soraya Brosset, Laure Drutel, Emeline Peyric, Ines Ben Abdallah, Dhaif Bekha, Sara Neumane, Edouard Duchesnay, Mickael Dinomais, Mathilde Chevignard, Lucie Hertz-Pannier
Publikováno v:
Frontiers in Neuroscience, Vol 18 (2024)
IntroductionEarly focal brain injuries lead to long-term disabilities with frequent cognitive impairments, suggesting global dysfunction beyond the lesion. While plasticity of the immature brain promotes better learning, outcome variability across in
Externí odkaz:
https://doaj.org/article/2cf7262ba82b49e98582ceaf93d807c0
Autor:
L. Lion-François, Juan Velazquez-Dominguez, L. Guibaud, Christelle Rougeot-Jung, Hélène Laurichesse Delmas, Emeline Peyric, Vincent des Portes, Massimiliano Rossi, Mona Massoud, Marie-France Bonnetain, O. Revol, Catherine Sarret, Anne Miret
Publikováno v:
European Journal of Paediatric Neurology
European Journal of Paediatric Neurology, 2020, 29, pp.92-100. ⟨10.1016/j.ejpn.2020.09.007⟩
European Journal of Paediatric Neurology, Elsevier, 2020, 29, pp.92-100. ⟨10.1016/j.ejpn.2020.09.007⟩
European Journal of Paediatric Neurology, 2020, 29, pp.92-100. ⟨10.1016/j.ejpn.2020.09.007⟩
European Journal of Paediatric Neurology, Elsevier, 2020, 29, pp.92-100. ⟨10.1016/j.ejpn.2020.09.007⟩
Objectives Rhombencephalosynapsis (RES) is a very rare cerebellar malformation. Neurodevelopmental outcome of apparently isolated RES remains poorly documented and standardized cognitive assessment, reported in only nine published cases so far, is la
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::153e00d3aff3aa7921713468fe2984f3
https://hal.science/hal-03124493
https://hal.science/hal-03124493
Autor:
Laurence Lion-François, Catherine Mercier, George A. Michael, Behrouz Kassai, Vincent Desportes, Virginie Coutinho, Daniel Gérard, Emeline Peyric, Vania Herbillon, Tiphanie Ginhoux, Isabelle Kemlin
Publikováno v:
Journal of attention disorders
Journal of attention disorders, 2020, 24 (13), pp.1807-1823. ⟨10.1177/1087054717707579⟩
Journal of attention disorders, 2020, 24 (13), pp.1807-1823. ⟨10.1177/1087054717707579⟩
International audience; Objective: To compare children with Neurofibromatosis type 1 and associated ADHD symptomatology (NF1 + ADHD) with children having received a diagnosis of ADHD without NF1. The idea was that performance differences in tasks of
Autor:
Amélie Clément, Marie-Pierre Cordier, Laurent Guibaud, Juan Velazquez-Dominguez, Pascal Gaucherand, François Rivier, Audrey Lacalm, Dorothée Ville, Mona Massoud, A. Rolland, Emeline Peyric, Aurore Curie, Anne-Sophie Pellot, Jérôme Massardier, Vincent des Portes
Publikováno v:
European Journal of Paediatric Neurology
European Journal of Paediatric Neurology, Elsevier, 2018, 22 (1), pp.82-92. ⟨10.1016/j.ejpn.2017.08.003⟩
European Journal of Paediatric Neurology, 2018, 22 (1), pp.82-92. ⟨10.1016/j.ejpn.2017.08.003⟩
European Journal of Paediatric Neurology, Elsevier, 2018, 22 (1), pp.82-92. ⟨10.1016/j.ejpn.2017.08.003⟩
European Journal of Paediatric Neurology, 2018, 22 (1), pp.82-92. ⟨10.1016/j.ejpn.2017.08.003⟩
International audience; Objectives : Neurodevelopmental outcome of apparently isolated agenesis of the corpus callosum (ACC) remains a major concern with uncertain prognosis. Despite “normal” IQ reported in a majority of patients, the rates of le
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::611427ef35ec6c226ae920f9a6e625fc
https://hal.umontpellier.fr/hal-01796396
https://hal.umontpellier.fr/hal-01796396
Autor:
Stéphane Chabrier, Emeline Peyric, Laure Drutel, Johanna Deron, Manoëlle Kossorotoff, Mickaël Dinomais, Leila Lazaro, Jérémie Lefranc, Guillaume Thébault, Gérard Dray, Joel Fluss, Cyrille Renaud, Sylvie Nguyen The Tich, Stéphane Darteyre, Céline Dégano, Matthieu Delion, Samuel Groeschel, Lucie Hertz-Pannier, Béatrice Husson, Emilie Presles, Magaly Ravel, Carole Vuillerot
Publikováno v:
The Journal of Pediatrics
The Journal of Pediatrics, 2016, 172, pp.156-161.e3. ⟨10.1016/j.jpeds.2016.01.069⟩
Journal of Pediatrics
Journal of Pediatrics, Elsevier, 2016, 172, pp.156-161.e3. ⟨10.1016/j.jpeds.2016.01.069⟩
The Journal of Pediatrics, Vol. 172 (2016) pp. 156-161.e3
The Journal of Pediatrics, 2016, 172, pp.156-161.e3. ⟨10.1016/j.jpeds.2016.01.069⟩
Journal of Pediatrics
Journal of Pediatrics, Elsevier, 2016, 172, pp.156-161.e3. ⟨10.1016/j.jpeds.2016.01.069⟩
The Journal of Pediatrics, Vol. 172 (2016) pp. 156-161.e3
Objectives To evaluate the epileptic, academic, and developmental status at age 7 years in a large population of term-born children who sustained neonatal arterial ischemic stroke (NAIS), and to assess the co-occurrence of these outcomes. Study desig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::298de0876d4139827318f1b2e84366c7
https://hal.science/hal-02099375
https://hal.science/hal-02099375
Autor:
Isabelle Tapiero, Emeline Peyric, Charline Madelaine, Laurence Lion-François, Pauline Mathey, George A. Michael
Publikováno v:
European Journal of Paediatric Neurology. 21:e69-e70
Autor:
J. Delpouve, L. Guibaud, Dorothée Ville, Christelle Rougeot, A. Benezit, M. Cagneaux, Emeline Peyric, Yves Paulignan, Alice C. Roy, V. des Portes
Publikováno v:
European Journal of Paediatric Neurology. 17:S111
Autor:
Stéphane Pinson, Virginie Coutinho, Catherine Mercier, Valentine Bréant, François Gueyffier, Patrick Combemale, Daniel Gérard, Laurence Lion-François, Isabelle Kemlin, Behrouz Kassai, Emeline Peyric, Vania Herbillon, Tiphanie Ginhoux, Vincent des Portes, Diana Rodriguez
Publikováno v:
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases, 2014, 9, pp.142. ⟨10.1186/s13023-014-0142-4⟩
Orphanet Journal of Rare Diseases, BioMed Central, 2014, 9, pp.142. ⟨10.1186/s13023-014-0142-4⟩
Orphanet Journal of Rare Diseases, 2014, 9, pp.142. ⟨10.1186/s13023-014-0142-4⟩
Orphanet Journal of Rare Diseases, BioMed Central, 2014, 9, pp.142. ⟨10.1186/s13023-014-0142-4⟩
et Réseau NF1 Rhône Alpes Auvergne-France; International audience; Background: Neurofibromatosis type 1 (NF1) is an autosomal dominant disorder with an estimated prevalence of about 1/3000, independent of ethnicity, race, or gender. Attention Defic
Autor:
Groeschel, Samuel, Hertz‐Pannier, Lucie, Delion, Matthieu, Loustau, Sébastien, Husson, Béatrice, Kossorotoff, Manoelle, Renaud, Cyrille, Nguyen The Tich, Sylvie, Chabrier, Stéphane, Dinomais, Mickaël, Darteyre, Stéphane, Dégano, Céline, Deron, Johanna, Dray, Gérard, Drutel, Laure, Lazaro, Leila, Lefranc, Jérémie, Peyric, Emeline, Presles, Emilie, Ravel, Magaly, Thébault, Guillaume, Vuillerot, Carole
Publikováno v:
Developmental Medicine and Child Neurology
Developmental Medicine and Child Neurology, Wiley-Blackwell, 2017, 59 (10), pp.1042-1048. ⟨10.1111/dmcn.13517⟩
Developmental Medicine and Child Neurology, 2017, 59 (10), pp.1042-1048. ⟨10.1111/dmcn.13517⟩
Developmental Medicine and Child Neurology, Wiley-Blackwell, 2017, 59 (10), pp.1042-1048. ⟨10.1111/dmcn.13517⟩
Developmental Medicine and Child Neurology, 2017, 59 (10), pp.1042-1048. ⟨10.1111/dmcn.13517⟩
International audience; AIM: The objective of this study was to investigate the involvement of the motor fibres of the corpus callosum after unilateral neonatal arterial ischemic stroke (NAIS) of the middle cerebral artery territory and the relations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0adeb33014d470af99aa2cc2b12746ea
https://hal.univ-angers.fr/hal-02510147
https://hal.univ-angers.fr/hal-02510147