Intelligence and Executive Functions: A Comprehensive Assessment of Intellectually Gifted Children
Bucaille, A, Jarry, C, Allard, J, Brosseau-Beauvir, A, Ropars, J, Brochard, S, Peudenier, S, Roy, A
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Published in Archives of clinical neuropsychology (20.10.2023)
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Clinical characteristics of COVID-19 infection in polyhandicapped persons in France
Rousseau, M.-C., Hully, M., Milh, M., Juzeau, D., Pollez, B., Peudenier, S., Bahi Buisson, N., Gautheron, V., Chabrol, B., Billette de Villemeur, T.
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.07.2021)
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.07.2021)
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Carney complex revealed by a cerebellar ischaemic stroke in a 6‐year‐old girl
Acquitter, M., Laparra, V., Brenaut, E., Peudenier, S., Teissier, R., Clauser, E., Misery, L., Abasq‐Thomas, C.
Published in Journal of the European Academy of Dermatology and Venereology (01.04.2018)
Published in Journal of the European Academy of Dermatology and Venereology (01.04.2018)
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Changes in muscle activation during gait of children with duchenne muscular dystrophy
Ropars, J., Lemeur, M., Vuillerot, C., Tiffreau, V., Peudenier, S., Cuisset, J. M., Pereon, Y., Leboeuf, F., Delporte, L., Delpierre, Y., Gross, R., Brochard, S.
Published in Computer methods in biomechanics and biomedical engineering (01.01.2015)
Published in Computer methods in biomechanics and biomedical engineering (01.01.2015)
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A survey of medical and paramedical involvement in children with cerebral palsy in Britanny: Preliminary results
Sacaze, E, Garlantezec, R, Rémy-néris, O, Peudenier, S, Rauscent, H, le Tallec, H, Bernier-Francois, V, Pichancourt, D, Brochard, S
Published in Annals of physical and rehabilitation medicine (01.05.2013)
Published in Annals of physical and rehabilitation medicine (01.05.2013)
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Effectiveness of nitrous oxide and analgesic cream (lidocaine and prilocaine) for prevention of pain during intramuscular botulinum toxin injections in children
Brochard, S, Blajan, V, Lempereur, M, Le Moine, P, Peudenier, S, Lefranc, J, Rémy-Néris, O
Published in Annals of physical and rehabilitation medicine (01.12.2009)
Published in Annals of physical and rehabilitation medicine (01.12.2009)
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Four Caucasian patients with mutations in the fukutin gene and variable clinical phenotype
Vuillaumier-Barrot, S, Quijano-Roy, S, Bouchet-Seraphin, C, Maugenre, S, Peudenier, S, Van den Bergh, P, Marcorelles, P, Avila-Smirnow, D, Chelbi, M, Romero, N.B, Carlier, R.Y, Estournet, B, Guicheney, P, Seta, N
Published in Neuromuscular disorders : NMD (01.03.2009)
Published in Neuromuscular disorders : NMD (01.03.2009)
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Promoting the use of Motor Function Measure (MFM) as outcome measure in patients with Duchenne Muscular Dystrophy (DMD) treated by corticosteroids
Schreiber-Bontemps, A, Brochard, S., Dr, Fontaine-Carbonnel, S., Dr, Chabrier, S., Dr, Gautheron, V., Dr, Peudenier, S., Dr, Rippert, P, Rauscent, H., Dr, Rivier, F., Dr, Andoni Urtizberea, J., Dr, Fournier-Mehouas, M., Dr, Mahé, J.Y., Dr, Tiffreau, V., Dr, Lagrue, E., Dr, Hamroun, D, Poirot, I., Dr, Ragot-Mandry, S., Dr, Sacconi, S., Dr, Puy Haubert, B, Fafin, C, Vuillerot, C., Dr
Published in Annals of physical and rehabilitation medicine (01.09.2015)
Published in Annals of physical and rehabilitation medicine (01.09.2015)
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Mitochondrial respiratory chain deficiency revealed by hypothermia
Cholley, F, Edery, P, Ricquier, D, Peudenier, S, Slama, A, Tardieu, M
Published in Neuropediatrics (01.04.2001)
Published in Neuropediatrics (01.04.2001)
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La douleur chez l’enfant en situation de handicap neurologique : mise au point de la Commission « déficience intellectuelle et handicap » de la Société française de neurologie pédiatrique
Avez-Couturier, J., Joriot, S., Peudenier, S., Juzeau, D.
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.01.2018)
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.01.2018)
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Corticosteroids in Duchenne muscular dystrophy: impact on the motor function measure sensitivity to change and implications for clinical trials
Schreiber, Audrey, Brochard, Sylvain, Rippert, Pascal, Fontaine‐Carbonnel, Stephanie, Payan, Christine, Poirot, Isabelle, Hamroun, Dalil, Vuillerot, Carole, Peudenier, Sylviane, Ropars, Juliette, Urtizberea, Andoni, Tiffreau, Vincent, Puyhaubert, Blandine, Fournier Mehouas, Manuella, Sacconi, Sabrina, Lagrue, Emmanuelle, Chabrier, Stéphane
Published in Developmental medicine and child neurology (01.02.2018)
Published in Developmental medicine and child neurology (01.02.2018)
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G.P.271
Marttila, M, Lehtokari, V.L, Marston, S.B, Nyman, T.A, Barnerias, C, Beggs, A.H, Bertin, E, Ceyhan-Birsoy, Ö, Cintas, P, Gerard, M, Gilbert-Dussardier, B, Hogue, J.S, Longman, C, Eymard, B, Frydman, M, Kang, P.B, Klinge, L, Kolski, H, Lochmüller, H, Magy, L, Manel, V, Mayer, M, North, K.N, Peudenier-Robert, S, Pihko, H, Probst, F.J, Reisin, R, Stewart, W, Taratuto, A.L, de Visser, M, Wilichowski, E, Winer, J, Nowak, K, Lain, N.G, Winder, T.L, Monnier, N, Clarke, N.F, Pelin, K, Grönholm, M, Wallgren-Pettersson, C
Published in Neuromuscular disorders : NMD (01.10.2014)
Published in Neuromuscular disorders : NMD (01.10.2014)
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A new case of Kaufman Oculocerebrofacial Syndrome caused by two new splicing variants in UBE3B
Uguen, K., Ka, C., Planes, M., Audebert-Bellanger, S., Redon, S., Benech, C., Kury, S., Peudenier, S., Autret, S., Gourlaouen, I., Bonneau, D., Odent, S., Bezieau, S., Gilbert-Dussardier, B., Boland, A., Deleuze, J., Le Marechal, C., Le Gac, G., Ferec, C.
Published in European journal of human genetics : EJHG (2020)
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Published in European journal of human genetics : EJHG (2020)
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Large-Scale Deletion and Point Mutations of the Nuclear NDUFV1 and NDUFS1 Genes in Mitochondrial Complex I Deficiency
Bénit, Paule, Chretien, Dominique, Kadhom, Nohman, de Lonlay-Debeney, Pascale, Cormier-Daire, Valérie, Cabral, Aguinaldo, Peudenier, Sylviane, Rustin, Pierre, Munnich, Arnold, Rötig, Agnès
Published in American journal of human genetics (01.06.2001)
Published in American journal of human genetics (01.06.2001)
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The DM-scope registry: a rare disease innovative framework bridging the gap between research and medical care
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
Published in Orphanet journal of rare diseases (01.06.2019)
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Published in Orphanet journal of rare diseases (01.06.2019)
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La douleur chez l’enfant en situation de handicap neurologique : mise au point de la Commission « déficience intellectuelle et handicap » de la Société française de neurologie pédiatrique
Avez-Couturier, J., Joriot, S., Peudenier, S., Juzeau, D.
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.01.2018)
Published in Archives de pédiatrie : organe officiel de la Société française de pédiatrie (01.01.2018)
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