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Annals of physical and rehabilitation medicine
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Ann Phys Rehabil Med
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Documents disponibles dans cette revue (27)
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Prada V ; Hamedani M ; Genovese F ; Zuppa A ; Benedetti L ; Bellone E ; Grandis M ; Mandich P ; Schenone A | 13/10/2020Article
Reynaud V ; Conforto I ; Givron P ; Clavelou P ; Cornut-Chauvinc C ; Taithe F ; Pereira B ; Coudeyre E | Netherlands | 02/2020Article
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Fontaine Carbonnel S, Auteur ; Rippert P ; Poirot I ; Gachet D ; de Lattre C ; Vuillerot C | 2016Abstrat no. CO021 OBJECTIVE: Since 2005, in France, corticosteroid therapy is now widely used in Duchenne muscular dystrophy (DMD). This treatment has changed our practice of pediatric rehabilitation teams. We describe here our 10-year clinical[...]Article
Abstract no. CO0217 OBJECTIVE: The "quality of life in neuromuscular disease" questionnaire (QoL-NMD) is a new health-related quality of life measurement tool specifically designed for patients with a slowly-progressive neuromuscular disease wi[...]Article
Tiffreau V, Auteur ; Tiffreau V ; Kopciuch F ; Thevenon A ; Rannou F ; Hachulla E ; Thoumie P | 2016Abstract no. CO020 OBJECTIVE: To evaluate the medium-term functional impact and effect on quality of life of a standardized rehabilitation programme in patients with polymyositis and dermatomyositis. MATERIALS/PATIENTS AND METHODS: Design: a mu[...]Article
Vuillerot C, Auteur ; Vincent-Genod D ; Thomann G ; Coton J | 2016Poster no. PO0110 OBJECTIVE: Physiotherapists are demanding of valid outcome measures to assess the evolution of their patient's motor functions in order to precisely describe the effects of treatments and the progress of diseases. Hence, sever[...]Article
Claire C, Auteur ; Martel M ; Fortin S ; Raymond MJ ; Veilleux LN ; D'Arcy S ; Lemay M | 2016Poster no. PO0103 OBJECTIVE: Charcot-Marie-Tooth disease (CMT) is a hereditary peripheral neuropathy and belongs to neuromuscular diseases. CMT affects motor function of children, but its clinical expressions are heterogeneous and it could also[...]Article
Ropars J, Auteur ; Lempereur M ; Brochard S ; Vuillerot C ; Tiffreau V ; Cuisset JM ; Pereon Y ; Leboeuf F ; Gross R ; Delporte L ; Delpierre Y | 2016Abstract no. CO023 OBJECTIVE: The aim of this prospective study was to investigate changes in muscle activity during gait in children with Duchenne muscular Dystrophy (DMD). MATERIALS/PATIENTS AND METHODS: Dynamic surface electromyography recor[...]Article
Sauvagnac-Quera R, Auteur ; Vabre C ; Azzi V ; Tirolien S ; Leiba N ; Poisson F ; Miladi L ; Carlier R ; Glorion C ; Leclair D ; Estournet B ; Quijano Roy S | 2016Abstract no. CO0266 OBJECTIVE: To evaluate the effectiveness of use of Garches Brace (GB) on prevention and treatment of scoliosis and its impact on quality of life, in a group of patients with spinal muscular atrophy (SMA) type Ib. MATERIAL/PA[...]Article
Conforto I, Auteur ; Coudeyre E | 2016Poster no. PO0137 OBJECTIVE: To evaluate the relation between prehension strength, dexterity and axonal loss in a same cohort of CMT1A patients with valid tools. CMT1A is the most common form of hereditary neuropathy. The upper limb impairment [...]Article
Poster no. PO0140 OBJECTIVE: Neuromuscular diseases (NMD) are frequently characterized by a progressive clinical course leading to disability, which has an impact also on the quality of life. To date, there is no evidence if the severity of dis[...]Article
Pellegrini N, Auteur | 2016Abstract no. CO022 OBJECTIVE: To study seated postural control in neuromuscular disorder. MATERIALS/PATIENTS AND METHODS: We conducted a retrospective observational cohort study of 130 neuromuscular adult patients having a positioning wheelchai[...]Article
de Lattre C, Auteur ; Rippert P ; Hmaroun D ; Sacconi S ; Poirot I ; Vuillerot C | 2016Poster no. PO0139 OBJECTIVE: To assess the applicability and the responsiveness of the motor function measure 1 (MFM) in a facio scapulo humeral dystrophy (FSHD) population. MATERIALS/PATIENTS AND METHODS: It is an observational, retrospective [...]Article
de Lattre C, Auteur ; Rippert P ; Bassez G ; Hamroun D ; Poirot I ; Vuillerot C | 2016Abstract no. CO019 OBJECTIVE: To assess the applicability and the responsiveness of the motor function measure 1 (MFM) in the myotonic dystrophy type 1 (DM1) population. MATERIALS/PATIENTS AND METHODS: We conducted an observational, retrospecti[...]Article
Hamonet-Torny J, Auteur | 2016Abstract no. CO014 OPINION/FEEDBACK: INTRODUCTION: Despite of the politique for social inclusion leaded since the last decade, many specialized institutions for disabled children remained in France. This institutional field is varied and hetero[...]Article
Allard L ; Rode G ; Jacquin-Courtois S ; Pouget MC ; Rippert P ; Hamroun D ; Poirot I ; Bérard C ; Vuillerot C ; Groupe d’étude CMT MFM | 2014Article
Rapin A ; Etossé A ; Tambosco L ; Nicomette J ; Percebois-Macadre L ; Mouret P ; Boyer FC | 2013Article
Kieny P ; Chollet S ; Delalande P ; Le Fort M ; Magot A ; Pereon Y ; Perrouin-Verbe B | 2013Article
Vuillerot C ; Rippert P ; Roche S ; Bérard C ; Margirier F ; de Lattre C ; Poirot I ; Berruyer A ; Tiffreau V ; Fournier-Mehouas M ; Bouhour F ; Urtizberea JA ; Renders A ; Ecochard R ; Groupe d'étude NM-Score ; Le Flem A ; Barrière A ; Rouyer AP ; Fontaine S ; Vadot JP ; Pupat EL ; Chartier Y ; Vincent-Genod D ; Girardot F ; Manel V ; Aubert F ; Rode G ; Denis D ; Germa V ; Quijanot S ; Pelligrini N ; d'Anjou MC ; Féasson L ; Chabrier S ; Furby A ; Goyet C ; Delmas MC ; Campech M ; Robert F ; Hovart H ; Cuisset JM ; Badoil I ; Fafin C ; Tanant V ; Sacconi S ; Gayraud JP ; Carpentier A ; Vanderschueren S ; Bourdeauducq I ; Salicio-Castillo D ; Cobo AM ; Commare MC ; Farigoule V ; Huzar C ; Berger B ; Humbertclaude V ; Rumeau F ; Viehweger E ; Payet-Laury C ; Pénisson-Besnier I ; Kinet V ; Laridant D ; Spehrs-Ciaffi V ; Bassez G ; Goemans N ; Pichancourt D ; Jezequel L ; Vedrenne N | 2013Article
Ribiere C ; Bernardin M ; Sacconi S ; Delmont E ; Fournier-Mehouas M ; Rauscent H ; Benchortane M ; Staccini P ; Lantéri-Minet M ; Desnuelle C | 2012Accès au résumé PubMed / to PubMed abstract Maladie de Charcot-Marie-Tooth : à propos d’une étude niçoise sur la douleur chez 50 patients La maladie de Charcot-Marie-Tooth (CMT) est une neuropathie héréditaire sensitivo-motrice carac[...]Article
Wagner S ; Poirot I ; Vuillerot C ; Bérard C | 2011Accès au résumé PubMed / to PubMed abstract 05/01/2012 - Des résultats probants pour le pamidronate dans l’ostéoporose chez l’enfant atteint de myopathie L’ostéoporose est une situation fréquemment rencontrée dans le suivi au long co[...]