Identification of wheelchair seating criteria in adults with neuromuscular diseases: A Delphi study von Dupitier, Elise, Voisin, Manon, Stalens, Caroline, Laforêt, Pascal, Pouplin, Samuel

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Motor Function Characteristics of Adults With Late-Onset Pompe Disease: A Systematic Scoping Review von Maulet, Théo, Bonnyaud, Celine, Weill, Catherine, Laforêt, Pascal, Cattagni, Thomas

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Update on new muscle glycogenosis von Laforêt, Pascal, Malfatti, Edoardo, Vissing, John

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Characterization of neuromuscular performances in adults with late-onset Pompe disease: a control case cross-sectional study von Maulet, Théo, Bonnyaud, Céline, Laforêt, Pascal, Cattagni, Thomas

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Disorders of muscle lipid metabolism: Diagnostic and therapeutic challenges von Laforet, Pascal, Vianey-Saban, Christine

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Muscle glycogen synthesis and breakdown are both impaired in glycogenin-1 deficiency von Stemmerik, Mads Godtfeldt, Madsen, Karen Lindhardt, Laforêt, Pascal, Buch, Astrid Emilie, Vissing, John

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Bezafibrate in skeletal muscle fatty acid oxidation disorders: A randomized clinical trial von Ørngreen, Mette Cathrine, Madsen, Karen Lindhardt, Preisler, Nicolai, Andersen, Grete, Vissing, John, Laforêt, Pascal

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Whole-body muscle MRI in McArdle disease von Tobaly, David, Laforêt, Pascal, Stojkovic, Tanya, Behin, Anthony, Petit, Francois Michael, Barp, Andrea, Bello, Luca, Carlier, Pierre, Carlier, Robert-Yves

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Mutations in dynamin 2 cause dominant centronuclear myopathy von Laporte, Jocelyn, Bitoun, Marc, Guicheney, Pascale, Ferrer, Xavier, Lacène, Emmanuelle, Lochmüller, Hanns, Fardeau, Michel, Maugenre, Svetlana, Jeannet, Pierre-Yves, Martin, Jean-Jacques, Laforêt, Pascal, Romero, Norma B, Eymard, Bruno, Beggs, Alan H

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Skeletal muscle metabolism is impaired during exercise in glycogen storage disease type III von Preisler, Nicolai, Laforêt, Pascal, Madsen, Karen Lindhardt, Prahm, Kira Philipsen, Hedermann, Gitte, Vissing, Christoffer Rasmus, Galbo, Henrik, Vissing, John

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Sarcoglycanopathies: state of the art and therapeutic perspectives von Fernández-Eulate, Gorka, Leturcq, France, Laforêt, Pascal, Richard, Isabelle, Stojkovic, Tanya

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Renal artery fibromuscular dysplasia in Pompe disease: A case report von Pappa, Evangelia, Papadopoulos, Constantinos, Grimbert, Philippe, Laforêt, Pascal, Bassez, Guillaume

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High risk of cancer in autoimmune necrotizing myopathies: usefulness of myositis specific antibody von Allenbach, Yves, Keraen, Jeremy, Bouvier, Anne-Marie, Jooste, Valérie, Champtiaux, Nicolas, Hervier, Baptiste, Schoindre, Yoland, Rigolet, Aude, Gilardin, Laurent, Musset, Lucile, Charuel, Jean-Luc, Boyer, Olivier, Jouen, Fabienne, Drouot, Laurent, Martinet, Jeremie, Stojkovic, Tanya, Eymard, Bruno, Laforêt, Pascal, Behin, Antony, Salort-Campana, Emmanuelle, Fain, Olivier, Meyer, Alain, Schleinitz, Nicolas, Mariampillai, Kuberaka, Grados, Aurelie, Benveniste, Olivier

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Late-onset Pompe disease in France: molecular features and epidemiology from a nationwide study von Semplicini, Claudio, Letard, Pascaline, De Antonio, Marie, Taouagh, Nadjib, Perniconi, Barbara, Bouhour, Françoise, Echaniz-Laguna, Andoni, Orlikowski, David, Sacconi, Sabrina, Salort-Campana, Emmanuelle, Solé, Guilhem, Zagnoli, Fabien, Hamroun, Dalil, Froissart, Roseline, Caillaud, Catherine, Laforêt, Pascal

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Recombinant human acid alpha-glucosidase (rhGAA) in adult patients with severe respiratory failure due to Pompe disease von Orlikowski, David, Pellegrini, Nadine, Prigent, Hélène, Laforêt, Pascal, Carlier, Robert, Carlier, Pierre, Eymard, Bruno, Lofaso, Frédéric, Annane, Djillali

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Cerebral vessel involvement in Pompe disease von Laforêt, Pascal, MD

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Resistant myasthenia gravis and rituximab: a monocentric retrospective study on 28 patients von Afanasiev, Vadim, Demeret, Sophie, Bolgert, Francis, Eymard, Bruno, Laforêt, Pascal, Benveniste, Olivier

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Correction: Cervical Spinal Cord Atrophy Profile in Adult SMN1-Linked SMA von El Mendili, Mohamed-Mounir, Lenglet, Timothée, Stojkovic, Tanya, Behin, Anthony, Guimarães-Costa, Raquel, Salachas, François, Meininger, Vincent, Bruneteau, Gaelle, Le Forestier, Nadine, Laforêt, Pascal, Lehéricy, Stéphane, Benali, Habib, Pradat, Pierre-François

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Glycogen storage disease type III: diagnosis, genotype, management, clinical course and outcome von Sentner, Christiaan P., Hoogeveen, Irene J., Weinstein, David A., Santer, René, Murphy, Elaine, McKiernan, Patrick J., Steuerwald, Ulrike, Beauchamp, Nicholas J., Taybert, Joanna, Laforêt, Pascal, Petit, François M., Hubert, Aurélie, Labrune, Philippe, Smit, G. Peter A., Derks, Terry G. J.

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Autologous Myoblast Transplantation for Oculopharyngeal Muscular Dystrophy: a Phase I/Iia Clinical Study von Périé, Sophie, Trollet, Capucine, Mouly, Vincent, Vanneaux, Valérie, Mamchaoui, Kamel, Bouazza, Belaïd, Marolleau, Jean Pierre, Laforêt, Pascal, Chapon, Françoise, Eymard, Bruno, Butler-Browne, Gillian, Larghero, Jérome, St Guily, Jean Lacau

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