Zobrazeno 1 - 10
of 130
pro vyhledávání: '"M L, Moutard"'
Autor:
A.-E. Millischer, D. Grevent, P. Sonigo, N. Bahi-Buisson, I. Desguerre, H. Mahallati, J.-P. Bault, T. Quibel, S. Couderc, M.-L. Moutard, E. Julien, V. Dangouloff, B. Bessieres, V. Malan, T. Attie, L.-J. Salomon, N. Boddaert
Publikováno v:
AJNR Am J Neuroradiol
BACKGROUND AND PURPOSE: Prognosis of isolated short corpus callosum is challenging. Our aim was to assess whether fetal DTI tractography can distinguish callosal dysplasia from variants of normal callosal development in fetuses with an isolated short
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::110fff0f61cdf43911ba78c3f347b89b
https://europepmc.org/articles/PMC8757544/
https://europepmc.org/articles/PMC8757544/
Autor:
Sophie Rondeau, Charles Coutton, Pierre-Simon Jouk, Lydie Burglen, Alice Goldenberg, Bérénice Doray, Nathalie Marle, Séverine Drunat, Pascal Chambon, P. Callier, Thierry Bienvenu, F. Devillard, M.-L. Moutard, Danielle Martinet, Bernard Aral, Pascale Saugier-Veber, Nathalie Perreton, Marie-Claude Addor, Marguerite Miguet, Martine Doco-Fenzy, N. Le Meur, Anne-Marie Guerrot, J.-L. Alessandri, C. Thauvin-Robinet, R. Touraine, Anne-Claude Tabet, Anne-Laure Mosca-Boidron, S. El Chehadeh, D. Devys, Sébastien Lebon, Alexandra Afenjar, Sandra Chantot-Bastaraud, Laurence Faivre, Emilie Landais, Cathy Philippe, Klaus Dieterich, Valérie Kremer, Julien Thevenon, Véronique Satre, V. des Portes, Francine Mugneret, Willie Reardon, Fabienne Prieur
Publikováno v:
Clinical Genetics. 91:576-588
Duplication of the Xq28 region, involving MECP2 (dupMECP2), has been primarily described in males with severe developmental delay, spasticity, epilepsy, stereotyped movements and recurrent infections. Carrier mothers are usually asymptomatic with an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e2ab2c2def825dc5de2fe9099d48486f
https://doi.org/10.1111/cge.12898
https://doi.org/10.1111/cge.12898
Autor:
E. Laracca, J. Nouet, Cécile Freihuber, M. Ardati, M.C. Rousseau, Stéphanie Valence, E. Grimont, M. Valkov, Anderson Loundou, D. Willocq, Agnès Felce, P. Sellier, S. Amalou, S. Lenormand, Diane Doummar, C. Brisse, Karine Baumstarck, J.C. Grasset, S. Haddadou, A. Belorgey, K. Maincent, M. Gaulard, M.H. Phan, Sherezad Khaldi-Cherif, J. Teulade, S. Delvert, Diana Rodriguez, J. Bonheur, Stéphane Pietra, V. Aynie, P. Julien, Arnaud Isapof, C. Coiffier, L. Luciani, Alexandra Afenjar, M.-L. Moutard, M.-C. Nougues, Bénédicte Héron, H. Si Abdelkader, Pascal Auquier, S. Mathieu, Thierry Billette de Villemeur, I. Kammache, Tanguy Leroy
Publikováno v:
Disability and Health Journal
Disability and Health Journal, 2019, 12 (4), pp.657-664. ⟨10.1016/j.dhjo.2019.01.013⟩
Disability and Health Journal, 2019, 12 (4), pp.657-664. ⟨10.1016/j.dhjo.2019.01.013⟩
Background Knowledge of the health status and care management of elderly individuals with polyhandicap* is lacking; however, a better understanding of the natural course of ageing in persons with severe and complex disability would help optimize prev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::510b5e21b49dc379c12fba3be7c13f63
https://hal.archives-ouvertes.fr/hal-03270176
https://hal.archives-ouvertes.fr/hal-03270176
Autor:
Christian Hervé, T. Billette de Villemeur, M.-L. Moutard, A.-O. Affdal, Grégoire Moutel, Nathalie Duchange
Publikováno v:
Archives de Pédiatrie. 22:337-342
Resume Objectif Le but de cette etude etait d’analyser les modalites de la transition des soins en epilepsie d’un service pediatrique vers un service pour adultes et par-la meme l’acquisition de l’autonomie du patient. Methode Notre enquete a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::02602fe0950bb43b2373c82f2deb71bd
https://doi.org/10.1016/j.arcped.2015.01.014
https://doi.org/10.1016/j.arcped.2015.01.014
Autor:
M. Cagneaux, Catherine Garel, J.-M. Jouannic, C. Rougeot, Mona Massoud, A. Benezit, N. Varene, M.-L. Moutard, Pascal Gaucherand, T. Billette, J. Massardier, V. Desportes, Laurent Guibaud
Publikováno v:
Ultrasound in Obstetrics & Gynecology. 44:447-454
Objective To define imaging patterns of unilateral cerebellar hypoplasia (UCH), discuss possible pathophysiological mechanisms and underline the etiology and prognosis associated with these lesions. Methods In this retrospective study we reviewed the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e24e549099f4a7ed12914767e4298c3
https://doi.org/10.1002/uog.13217
https://doi.org/10.1002/uog.13217
Autor:
S, El Chehadeh, R, Touraine, F, Prieur, W, Reardon, T, Bienvenu, S, Chantot-Bastaraud, M, Doco-Fenzy, E, Landais, C, Philippe, N, Marle, P, Callier, A-L, Mosca-Boidron, F, Mugneret, N, Le Meur, A, Goldenberg, A-M, Guerrot, P, Chambon, V, Satre, C, Coutton, P-S, Jouk, F, Devillard, K, Dieterich, A, Afenjar, L, Burglen, M-L, Moutard, M-C, Addor, S, Lebon, D, Martinet, J-L, Alessandri, B, Doray, M, Miguet, D, Devys, P, Saugier-Veber, S, Drunat, B, Aral, V, Kremer, S, Rondeau, A-C, Tabet, J, Thevenon, C, Thauvin-Robinet, N, Perreton, V, Des Portes, L, Faivre
Publikováno v:
Clinical genetics. 91(4)
Duplication of the Xq28 region, involving MECP2 (dupMECP2), has been primarily described in males with severe developmental delay, spasticity, epilepsy, stereotyped movements and recurrent infections. Carrier mothers are usually asymptomatic with an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1e8b3dfd3e37ae28d0d579ffbb2e0a79
https://pubmed.ncbi.nlm.nih.gov/27761913
https://pubmed.ncbi.nlm.nih.gov/27761913
Autor:
M.-L. Moutard, V. Desportes, V. d'Hardemare, Diane Doummar, Nathalie Dorison, Philippe Coubes, M. Vidailhet
Publikováno v:
European Journal of Paediatric Neurology. 21:e179-e180
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::15585f8790a8a1b1eb63dc2512b6ab1e
https://doi.org/10.1016/j.ejpn.2017.04.1113
https://doi.org/10.1016/j.ejpn.2017.04.1113
Autor:
François Chalard, E. Blondiaux, Catherine Garel, M.-L. Moutard, Amira Dhouib, Jean-Marie Jouannic, T Billette de Villemeur, H. Ducou Le Pointe
Publikováno v:
Ultrasound in Obstetrics & Gynecology. 38:170-178
Objectives To evaluate the diagnostic accuracy of fetal cerebral magnetic resonance imaging (MRI) on a large cohort and to compare pre- and postnatal MRI data. Methods This prospective study included all cases referred to our unit for fetal cerebral
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ae759184a397285ad5fb8bd2088b820d
https://doi.org/10.1002/uog.8937
https://doi.org/10.1002/uog.8937
Autor:
T. Billette de Villemeur, Catherine Garel, E. Raffo, M.-L. Moutard, S. Sacco, Arnaud Isapof, Fanny Lewin, Catherine Adamsbaum, J.-M. Jouannic, Antoinette Gelot, Virginie Kieffer
Publikováno v:
Archives de Pédiatrie. 17:226-232
The purpose of this study was to investigate the changes between 2000 and 2006 in pregnancy outcome when a diagnosis of either isolated or associated fetal corpus callosum agenesis (CCA) was made, given that beginning in 2003, the information provide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d1e42453503191bce729c2d1bde7670
https://doi.org/10.1016/j.arcped.2009.10.029
https://doi.org/10.1016/j.arcped.2009.10.029
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