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A Movement Monitor Based on Magneto-Inertial Sensors for Non-Ambulant Patients with Duchenne Muscular Dystrophy: A Pilot Study in Controlled Environment. [electronic resource] by
- Le Moing, Anne-Gaëlle
- Seferian, Andreea Mihaela
- Moraux, Amélie
- Annoussamy, Mélanie
- Dorveaux, Eric
- Gasnier, Erwan
- Hogrel, Jean-Yves
- Voit, Thomas
- Vissière, David
- Servais, Laurent
Producer: 20170718
In:
PloS one vol. 11
Availability: No items available.
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Effects of Methylphenidate on Default-Mode Network/Task-Positive Network Synchronization in Children With ADHD. [electronic resource] by
- Querne, Laurent
- Fall, Sidy
- Le Moing, Anne-Gaëlle
- Bourel-Ponchel, Emilie
- Delignières, Aline
- Simonnot, Anais
- de Broca, Alain
- Gondry-Jouet, Catherine
- Boucart, Muriel
- Berquin, Patrick
Producer: 20180528
In:
Journal of attention disorders vol. 21
Availability: No items available.
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EGR2 mutation enhances phenotype spectrum of Dejerine-Sottas syndrome. [electronic resource] by
- Gargaun, Elena
- Seferian, Andreea Mihaela
- Cardas, Ruxandra
- Le Moing, Anne-Gaelle
- Delanoe, Catherine
- Nectoux, Juliette
- Nelson, Isabelle
- Bonne, Gisèle
- Bihoreau, Marie-Thérèse
- Deleuze, Jean-François
- Boland, Anne
- Masson, Cécile
- Servais, Laurent
- Gidaro, Teresa
Producer: 20170407
In:
Journal of neurology vol. 263
Availability: No items available.
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EML1-associated brain overgrowth syndrome with ribbon-like heterotopia. [electronic resource] by
- Oegema, Renske
- McGillivray, George
- Leventer, Richard
- Le Moing, Anne-Gaëlle
- Bahi-Buisson, Nadia
- Barnicoat, Angela
- Mandelstam, Simone
- Francis, David
- Francis, Fiona
- Mancini, Grazia M S
- Savelberg, Sanne
- van Haaften, Gijs
- Mankad, Kshitij
- Lequin, Maarten H
Producer: 20200505
In:
American journal of medical genetics. Part C, Seminars in medical genetics vol. 181
Availability: No items available.
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Longitudinal functional and NMR assessment of upper limbs in Duchenne muscular dystrophy. [electronic resource] by
- Hogrel, Jean-Yves
- Wary, Claire
- Moraux, Amélie
- Azzabou, Noura
- Decostre, Valérie
- Ollivier, Gwenn
- Canal, Aurélie
- Lilien, Charlotte
- Ledoux, Isabelle
- Annoussamy, Mélanie
- Reguiba, Nacera
- Gidaro, Teresa
- Le Moing, Anne Gaelle
- Cardas, Ruxandra
- Voit, Thomas
- Carlier, Pierre G
- Servais, Laurent
Producer: 20160728
In:
Neurology vol. 86
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Congenital muscular dystrophy phenotype with neuromuscular spindles excess in a 5-year-old girl caused by HRAS mutation. [electronic resource] by
- Bolocan, Anamaria
- Quijano-Roy, Susana
- Seferian, Andreea M
- Baumann, Clarisse
- Allamand, Valérie
- Richard, Pascale
- Estournet, Brigitte
- Carlier, Robert
- Cavé, Hélène
- Gartioux, Corine
- Blin, Nathalie
- Le Moing, Anne-Gaëlle
- Gidaro, Teresa
- Germain, Dominique P
- Fardeau, Michel
- Voit, Thomas
- Servais, Laurent
- Romero, Norma Beatriz
Producer: 20150720
In:
Neuromuscular disorders : NMD vol. 24
Availability: No items available.
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Molecular characterization of a cohort of 73 patients with infantile spasms syndrome. [electronic resource] by
- Boutry-Kryza, Nadia
- Labalme, Audrey
- Ville, Dorothee
- de Bellescize, Julitta
- Touraine, Renaud
- Prieur, Fabienne
- Dimassi, Sarra
- Poulat, Anne-Lise
- Till, Marianne
- Rossi, Massimiliano
- Bourel-Ponchel, Emilie
- Delignières, Aline
- Le Moing, Anne-Gaelle
- Rivier, Clotilde
- des Portes, Vincent
- Edery, Patrick
- Calender, Alain
- Sanlaville, Damien
- Lesca, Gaetan
Producer: 20151130
In:
European journal of medical genetics vol. 58
Availability: No items available.
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Non-Ambulant Duchenne Patients Theoretically Treatable by Exon 53 Skipping have Severe Phenotype. [electronic resource] by
- Servais, Laurent
- Montus, Marie
- Guiner, Caroline Le
- Ben Yaou, Rabah
- Annoussamy, Mélanie
- Moraux, Amélie
- Hogrel, Jean-Yves
- Seferian, Andreea M
- Zehrouni, Karima
- Le Moing, Anne-Gaëlle
- Gidaro, Teresa
- Vanhulle, Catherine
- Laugel, Vincent
- Butoianu, Nina
- Cuisset, Jean-Marie
- Sabouraud, Pascal
- Cances, Claude
- Klein, Andrea
- Leturcq, France
- Moullier, Philippe
- Voit, Thomas
Publication details: Journal of neuromuscular diseases Sep 2015
In:
Journal of neuromuscular diseases vol. 2
Availability: No items available.
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11.
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Upper limb evaluation and one-year follow up of non-ambulant patients with spinal muscular atrophy: an observational multicenter trial. [electronic resource] by
- Seferian, Andreea Mihaela
- Moraux, Amélie
- Canal, Aurélie
- Decostre, Valérie
- Diebate, Oumar
- Le Moing, Anne Gaëlle
- Gidaro, Teresa
- Deconinck, Nicolas
- Van Parys, Frauke
- Vereecke, Wendy
- Wittevrongel, Sylvia
- Annoussamy, Mélanie
- Mayer, Michèle
- Maincent, Kim
- Cuisset, Jean-Marie
- Tiffreau, Vincent
- Denis, Severine
- Jousten, Virginie
- Quijano-Roy, Susana
- Voit, Thomas
- Hogrel, Jean-Yves
- Servais, Laurent
Producer: 20160331
In:
PloS one vol. 10
Availability: No items available.
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Mutations in Eml1 lead to ectopic progenitors and neuronal heterotopia in mouse and human. [electronic resource] by
- Kielar, Michel
- Tuy, Françoise Phan Dinh
- Bizzotto, Sara
- Lebrand, Cécile
- de Juan Romero, Camino
- Poirier, Karine
- Oegema, Renske
- Mancini, Grazia Maria
- Bahi-Buisson, Nadia
- Olaso, Robert
- Le Moing, Anne-Gaëlle
- Boutourlinsky, Katia
- Boucher, Dominique
- Carpentier, Wassila
- Berquin, Patrick
- Deleuze, Jean-François
- Belvindrah, Richard
- Borrell, Victor
- Welker, Egbert
- Chelly, Jamel
- Croquelois, Alexandre
- Francis, Fiona
Producer: 20140822
In:
Nature neuroscience vol. 17
Availability: No items available.
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13.
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Upper limb strength and function changes during a one-year follow-up in non-ambulant patients with Duchenne Muscular Dystrophy: an observational multicenter trial. [electronic resource] by
- Seferian, Andreea Mihaela
- Moraux, Amélie
- Annoussamy, Mélanie
- Canal, Aurélie
- Decostre, Valérie
- Diebate, Oumar
- Le Moing, Anne-Gaëlle
- Gidaro, Teresa
- Deconinck, Nicolas
- Van Parys, Frauke
- Vereecke, Wendy
- Wittevrongel, Sylvia
- Mayer, Michèle
- Maincent, Kim
- Desguerre, Isabelle
- Thémar-Noël, Christine
- Cuisset, Jean-Marie
- Tiffreau, Vincent
- Denis, Severine
- Jousten, Virginie
- Quijano-Roy, Susana
- Voit, Thomas
- Hogrel, Jean-Yves
- Servais, Laurent
Producer: 20151016
In:
PloS one vol. 10
Availability: No items available.
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14.
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Phenotype-genotype correlations in 17 new patients with an Xp11.23p11.22 microduplication and review of the literature. [electronic resource] by
- Nizon, Mathilde
- Andrieux, Joris
- Rooryck, Caroline
- de Blois, Marie-Christine
- Bourel-Ponchel, Emilie
- Bourgois, Béatrice
- Boute, Odile
- David, Albert
- Delobel, Bruno
- Duban-Bedu, Bénédicte
- Giuliano, Fabienne
- Goldenberg, Alice
- Grotto, Sarah
- Héron, Delphine
- Karmous-Benailly, Houda
- Keren, Boris
- Lacombe, Didier
- Lapierre, Jean-Michel
- Le Caignec, Cédric
- Le Galloudec, Eric
- Le Merrer, Martine
- Le Moing, Anne-Gaëlle
- Mathieu-Dramard, Michèle
- Nusbaum, Sylvie
- Pichon, Olivier
- Pinson, Lucile
- Raoul, Odile
- Rio, Marlène
- Romana, Serge
- Roubertie, Agnès
- Colleaux, Laurence
- Turleau, Catherine
- Vekemans, Michel
- Nabbout, Rima
- Malan, Valérie
Producer: 20150818
In:
American journal of medical genetics. Part A vol. 167A
Availability: No items available.
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