Search Results - "Durigneux, J."

Opsoclonus in a child with neuroborreliosis: Case report and review of the literature by Gibaud, M., Pauvert, O., Gueden, S., Durigneux, J., Van Bogaert, P.

“…Opsoclonus consists of massive erratic rapid eye jerks. They may occur in isolation or in association with myoclonus and ataxia, i.e., opsoclonus-myoclonus…”
Get full text

Genetic background of Moyamoya syndrome: report of 3 new cases by Gueden, S, Gibaud, M, Durigneux, J, Delion, M, Colin, E, Van Bogaert, P

Get full text

Corrigendum to “22nd International Congress of the World Muscle Society, Saint Malo, France, 3rd–7th October 2017” [Neuromuscular Disorders 27S2 (2017) S51–S270] by Rendu, J., Bosson, C., Roux-Buisson, N., Chatagnon, A., Bankole, B., Rivier, F., Durigneux, J., Monges, S., Stojkovic, T., Romero, N., Marty, I., Fauré, J.

Get full text

Cervicocephalic correction mattress: A new therapy in plagiocephaly and torticollis by Durigneux, J, Dinomais, M, Chevalier, B, Marquois, L, Payneau, G, Deries, X

Get full text

Development, activities and orientations of multidisciplinary consultations for neuromuscular diseases of the Nantes-Angers Reference center for rare diseases by Mahe, J.-Y, Kieny, P, N’guyen Te Tich, S, Perrier, J, Magot, A, Durigneux, J, Deries, X, David, A, Isidor, B, Le Fort, M, Mussini, J.-M, Perraud-Gouin, A.-S, Liorit, C, Chasserrieau, R, Chevalier, B, Lafaye-Meret, N, Penisson, I, Pereon, Y

Get full text

Matelas de correction cervico-céphalique : nouveau traitement du torticolis et de la plagiocéphalie du nourrisson by Durigneux, J, Dinomais, M, Chevalier, B, Marquois, L, Payneau, G, Deries, X

Get full text

SMA - CLINICAL: P.85 Evolution at 18 months of SMA type 1 patients treated with nusinersen by De Lucia, S., Phelep, A., Seferian, A., Foyer, P., Walther-Louvier, U., Durigneux, J., Cances, C., Ropars, J., Vuillerot, C., Servais, L., Boespflug, O.

Get full text

SMA - CLINICAL by De Lucia, S., Phelep, A., Seferian, A., Foyer, P., Walther-Louvier, U., Durigneux, J., Cances, C., Ropars, J., Vuillerot, C., Servais, L., Boespflug, O.

Get full text

P.62 - Genotype-phenotype correlations in a French cohort with Becker muscular dystrophy: focus on cognitive aspects by Dahimene, F., Nadej-Pakleza, A., Durigneux, J., Mercier, S., Pereon, Y., Magot, A.

Get full text

Genotype-phenotype correlations in a French cohort with Becker muscular dystrophy: focus on cognitive aspects by Dahimene, F., Nadej-Pakleza, A., Durigneux, J., Mercier, S., Pereon, Y., Magot, A.

Get full text

Évolution, activités et orientations des consultations multidisciplinaires des maladies neuromusculaires du centre de référence des maladies rares Nantes-Angers by Mahe, J.-Y, Kieny, P, N’guyen Te Tich, S, Perrier, J, Magot, A, Durigneux, J, Deries, X, David, A, Isidor, B, Le Fort, M, Mussini, J.-M, Perraud-Gouin, A.-S, Liorit, C, Chasserrieau, R, Chevalier, M.-B, Lafaye-Meret, N, Penisson, I, Pereon, Y

Get full text

SMA – THERAPY by Goff, L. Le, Seferian, A., Phelep, A., Rippert, P., Mathieu, M., Cances, C., de Lattre, C., Durigneux, J., Gousse, G., Quijano-Roy, S., Sarret, C., Servais, L., Vuillerot, C.

Get full text

SMA – THERAPY: P.278 Use of motor function measure-20 (MFM-20) to monitor SMA type 1 and 2 patients under nusinersen by Goff, L. Le, Seferian, A., Phelep, A., Rippert, P., Mathieu, M., Cances, C., de Lattre, C., Durigneux, J., Gousse, G., Quijano-Roy, S., Sarret, C., Servais, L., Vuillerot, C.

Get full text

P-465 – Manifestations sévères de migraine hémiplégique sporadique: difficultés diagnostiques en aigu by Dumortier, M., Durigneux, J., Beaumesnil, M., Nguyen, S., Gueden, S.

Get full text

P-290 – Scoliose infantile idiopathique. À propos d'un cas by Rousseau, A., Dinomais, M., Parent, H.F., Durigneux, J.

Get full text

P-468 – Syndrome de Guillain Barré: une complication inhabituelle by Molines, L., Gueden, S., Delion, M., Ollivier, M., Durigneux, J., Nguyen, S., De La Vaissière, S.

Get full text

The DM-scope registry: a rare disease innovative framework bridging the gap between research and medical care by de Antonio, M, Dogan, C, Eymard, B, Puymirat, J, Mathieu, J, Gagnon, C, Attarian, S, Aube-Nathier, Ac, Audic, F, Bach, N, Barnerias, C, Bedat-Millet, Al, Behin, A, Bellance, R, Ben Yaou, R, Bombard, V, Bouhour, F, Boutte, C, Boyer, F, Cances, C, Chabrol, B, Chanson, Jb, Chapon, F, Chasseriau, R, Cintas, P, Cobo, Am, Colombert, V, Cruz, Mc, Cuisset, Jm, Deschamps, R, Desguerre, I, Durigneux, J, Duval, F, Espil, C, Fafin, C, Feasson, L, Fradin, M, Furby, A, Goldenberg, A, Grotto, S, Ghorab, K, Guyant-Marechal, L, Heron, D, Isapof, A, Jacquin-Piques, A, Journel, H, Laforet, P, Lagrue, E, Laroche-Raynaud, C, Laugel, V, Lebeau, F, Magot, A, Manel, V, Mayer, M, Mercier, S, Menard, D, Michaud, M, Minot, Mc, Morales, Rj, Nadaj-Pakleza, A, Noury, Jb, Pasquier, L, Pellieux, S, Pereon, Y, Perrier, J, Peudenier, S, Preudhomme, M, Pouget, J, Quijano-Roy, S, Ragot-Mandry, S, Richelme, C, Rivier, F, Sabouraud, P, Sacconi, S, Salort-Campana, E, Sarret, C, Schaeffer, S, Sole, G, Stojkovic, T, Taithe, F, Testard, H, Tiffereau, V, Urtizberea, A, Vanhulle, C, Vial, C, Walther-Louvier, U, Zagnoli, F, Hamroun, D, Bassez, G

“…Background: The relevance of registries as a key component for developing clinical research for rare diseases (RD) and improving patient care has been…”
Get full text