Mots-clés
> MYOBASE > INFORMATION-COMMUNICATION > communication > événement > colloque
colloqueSynonyme(s)abstract ;acte de colloque ;conférence ;congrès ;journée ;séminaire ;work shop ;workshop ;rencontre symposium |
Documents disponibles dans cette catégorie (3074)
Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Laumonier T ; Hoffmeyer P ; Menetrey J | 2011Myoblast transplantation remains a promising therapeutic approach in the treatment of several muscular disorders including Duchenne Muscular Dystrophy. Nevertheless, such therapies are limited by a massive early cell death following injections. [...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Galletta E ; Saletti C ; Pasut A ; Malerba A ; Vitiello L | 2011The interplay between macrophages and muscle precursors is known to be critical for muscle repair and regeneration. In the past, we have already reported that themurine macrophage cell line J774 can produce a macrophage-conditioned medium (MCM) [...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Chekiri A ; Abdelhak S ; Hakem D ; Takheroubt K ; Berrah A ; Chaouch M ; Masmoudi AN ; Baba-Ahmed R | 2011INTRODUCTION Idiopathic inflammatory myopathies are a heterogeneous group of diseases including dermatomyositis, polymyositis and inclusion body myositis. It'simportant to diagnose these entities because they are potentially treatable. The aim o[...]Article
IXèmes Journées Annuelles de la Société française de Myologie (SFM) (3-5 novembre 2011; Angers) ; Milea D | 2011La maladie de Steinert, pathologie neuromusculaire autosomique dominante, a des manifestations systémiques variées, sous forme d'atteintes cardiaques, respiratoires, gastrointestinales, endocriniennes, mais aussi oculaires. Les manifestations ne[...]Article
Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Borgne FL ; Logerot M ; Guyot S ; Demarquoy J | 2011The metabolic alterations occurring in DMD cells have been little studied. This metabolic aspect of the disease has an obvious interest since metabolic alterations arising in muscle cells lead to an altered energy production that may contribute [...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Puymirat J ; Bouchard JP ; Mathieu J | 2011Objective: To evaluate the efficacy and tolerability of methylphenidate for the treatment of excessive daytime somnolence (EDS) in patients with myotonic dystrophytype 1(DM1). Methods: twenty-four patients with DM1 with the Epworth Sleepiness sc[...]Article
SRF (Serum Response Factor) is a MADS box transcription factor that regulates the expression of numerous genes involved in contraction, signaling or energy metabolism. Cardiac-specific Cre/loxP mediated inactivation of SRF leads to reduced contr[...]Article
Degerny C ; Pinna G ; Maury Y ; Kratassiouk G ; Mouly V ; Frandsen N ; Harel-Bellan A | AFM-TELETHON | 2011MicroRNAs (miRNAs) are key molecules in cell biology. Here, we used a genome-wide miRNA loss-of-function screen based on LNA antisense oligonucleotides in order to identify miRNAs that are essential for terminal differentiation of human skeletal[...]Article
IXèmes Journées Annuelles de la Société française de Myologie (SFM) (3-5 novembre 2011; Angers) ; Furling D | 2011La Dystrophie Myotonique de type I (DM1) est une des maladies neuromusculaires les plus fréquentes chez l'adulte. La mutation responsable de cette maladie autosomique dominante est une expansion de triplets CTG localisée dans la région 3' non-co[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Desaphy JF ; Carbonara R ; Costanza T ; Muraglia M ; Corbo F ; Lentini G ; Franchini C ; Conte Camerino D | 2011Mexiletine (Mex) and tocainide (Toc) are two sodium channel blockers marketed as class IB antiarrhythmic drugs and used off label as antimyotonic drug. In particular, Mex is considered as the first choice drug by many and a clinical trial is goi[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Bastide B ; Cieniewski-Bernard C ; Montel V | 2011O-N-acetylglucosaminylation, termed O-GlcNAcation (O-GlcNAc), is a reversible post-translational modification which presents a dynamic and highly regulated interplay with phosphorylation. New insights strongly suggest that this atypical glycosyl[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Dupont E ; Cieniewski-Bernard C ; Bastide B ; Stevens L | 2011Numerous investigations provided strong evidence that the modulation of the activity of specific cell signaling pathways has an important role in neuromuscular disease progression and the development of therapies. We analyzed the role of PI3K-AK[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Karmouch J ; Sigoillot S ; Bourgeois F ; Krejci E ; Chevalier C ; Houlgatte R ; Leger J ; Legay C | 2011Congenital myasthenic syndromes (CMS) correspond to a class of human pathologies resulting from mutations in genes expressed at the neuromuscular junction (NMJ). These disorders are characterized by a dysfunction of the NMJ leading to muscle wea[...]Article
Escobar Cedillo RE ; Miranda A ; Ruano L ; Fernandez F ; Urtizberea JA ; Martinez E ; Krahn M ; Guizar R | 2011Introduction. Limb-girdle muscular dystrophy (LGMD) encompasses a genetically heterogeneous group of disorders characterized by proximal muscle weakness with adominant or recessive inheritance. One of the involved genes is the dysferlin. Dysfe[...]Article
Muscle cell formation is a coordinated process of tissue-specific gene expression, proliferation and differentiation. In order to safeguard the developing progenitor cells against a prolonged proliferation or a premature differentiation, cell cy[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Delalande O ; Del Giudice E ; Hubert JF ; Le Rumeur E | 2011Dystrophin is a long filamentous protein, its central region is made by 24 successive spectrin-like repeats structured in a coiled-coil (bundle of three alpha-helices) arrangement [1]. Its biological function is essential for keeping the integri[...]Article
Tolar J ; Adair JE ; Antoniou M ; Bartholomae CC ; Becker PS ; Blazar BR ; Bueren J ; Carroll T ; Cavazzana-Calvo M ; Clapp DW ; Dalgleish R ; Galy A ; Gaspar HB ; Hanenberg H ; von Kalle C ; Kiem HP ; Lindeman D ; Naldini L ; Navarro S ; Renella R ; Rio P ; Sevilla J ; Schmidt M ; Verhoeyen E ; Wagner JE ; Williams DA ; Thrasher AJ | 2011Accès au résumé PubMed / to PubMed abstractArticle
Erratico S ; Villa C ; Razini P ; Cassinelli LM ; Parolini D ; Meregalli M ; Belicchi M ; Torrente Y | AFM-TELETHON | 2011Peripheral blood is a promising alternative source of stem cells for transplantation for the treatment of different malignancies. Using CD133, as a marker of stemness, we identified a subpopulation of purified blood-derived stem cells which diff[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Karine C ; Daniele N ; Florence L ; Vihola A ; Roudaut C ; Monjaret F ; Pion D ; Tarrade A ; Sarparanta J ; Udd B ; Richard I | 2011Titin is a giant protein expressed in both skeletal and cardiac muscles. Several pathogenic mutations were identified in its two last exons causing muscular dystrophy phenotypes. The most common mutation, FINmaj, results in the replacement of 4 [...]Article
Renou L ; Papadopoulos A ; Beuvin M ; Lacene E ; Arimura T ; Gruenbaum Y ; Bonne G | AFM-TELETHON | 2011LMNA gene encodes for lamins A/C, ubiquitous proteins of the nuclear envelope in post-mitotic cells. Lamin A/C are thought to have structural but also essential regulatory roles in various signalization pathways by interactions with transcriptio[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Bertrand A ; Renou L ; Papadopoulos A ; Beuvin M ; Lacene E ; Arimura T ; Gruenbaum Y ; Bonne G | 2011LMNA gene encodes for lamins A/C, ubiquitous proteins of the nuclear envelope in post-mitotic cells. Lamin A/C are thought to have structural but also essential regulatory roles in various signalization pathways by interactions with transcriptio[...]Article
AFM-TELETHON 2011Dystrophin, with its modular structure, and in particular its central domain made up of 24 spectrin-like repeat motifs, is a protein that can support the deletion of certain internal areas provided that the final reading frame is preserved. Taki[...]Article
During embryonic development and embryonic stem cell (ESC) differentiation, the different cells forming the mature heart arise from the differentiation of two types of multipotent cardiovascular progenitors (MCPs). Using mouse embryonic stem cel[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; van den Berg L ; Drost M ; Schaart G ; de Laat J ; van Doorn P ; van der Ploeg A ; Reuser A | 2011Background: Pompe disease is an inherited lysosomal glycogen storage disorder caused by the deficiency of acid a-glucosidase. Skeletal muscle damage is attributed to lysosomal rupture and the release of glycogen and lysosomal enzymes into the cy[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Brigite M ; Adriouch S ; Authier FJ ; Boyer O ; Gherardi RK ; Chrétien F | 2011Myology textbooks describe muscle fibroblasts on the grounds of EM studies as independent cells and envisage them only as collagen-producing cells. Lack of muscle fibroblast marker likely represents one cause of our ignorance about this cell sub[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Chen SF | 2011Purpose: To study the ultrastructural changes of muscle in patients with cerebrotendinous xanthomatosis (CTX) and make a correlation with the Tc99m-sestamibi thighSPECT/CT images (a noninvasive tool for the evaluation of the mitochondrial status[...]Article
Fugier C ; Vassilopoulos S ; Vignaud A ; Ferry A ; François V ; Precigout G ; Garcia L ; Butler-Browne GS ; Charlet Berguerand N ; Furling D | AFM-TELETHON | 2011Myotonic dystrophy type 1 (DM1) is the most common adult-onset muscular dystrophy. This disease is characterized, among other symptoms, by progressive muscle atrophy and weakness, myotonia and cardiac defects. DM1 is an autosomal dominant diseas[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Del Fraro G ; Meregalli M ; Farini A ; Belicchi M ; Parolini D ; Razini P ; Cassinelli L ; Angeloni V ; Maciotta S ; Bresolin N ; de Silva Bizario J ; Garcia L ; Torrente Y | 2011In DMD, skeletal and cardiac muscles are affected, leading to wheelchair dependency, respiratory failure and premature death. A combination of different strategies might enhance the possibility of successful therapy. We isolated CD133+ cells fro[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Bonnamy B ; Barrey E ; Mata X ; Chaffaux S ; Guerin G | 2011MicroRNAs (miRNA) are small endogenous non-coding interfering RNA molecules (18-25 nucleotides) regarded as major regulators in eukaryotic gene expression. They play a role in developmental timing, cellular differentiation, signaling and apoptos[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Bel C ; Bidault des Chaumes A ; Mahaut I ; Orssaud L | 2011What is Myobase ?Myobase is a bilingual database (French/English) which provides access to bibliographic information updated daily in the field of myology and motor handicap. It is implemented by the AFM Library. What would you find in Myobase ?[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Lambert V ; Capderou A ; Gouadon E ; Le Bret E ; Rucker-Martin C ; Dinanian S ; Stos B ; Renaud JF | 2011Purpose: Advances in cardiac surgery have improved short-term prognoses of patients with congenital heart diseases but, at long-term, right ventricular (RV) failure may occur, leading to morbidity and mortality. As conventional therapy gives poo[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Clément N ; Pisani D ; Sacconi S ; Desnuelle C ; Dani C ; Dechesne CA | 2011INTRODUCTION: Muscle-derived cells are able to differentiate towards osteogenic, chondrogenic or adipogenic lineage, in addition of their myogenic potential. Thisraises many biological and clinical questions. The cellular bases and the role of t[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Espartaco R ; Margaret M ; Eck P ; Leroy F ; Moirot P ; Lamy T ; Françoise C | 2011An obese (1m65, 105 kg) woman presented since the age of 53 years, in 2002, a facial weakness, initially left, then bilateral, associated with an hypoesthesia in the territory of the lower branch of the fifth cranial nerve and with a paralysis o[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Etienne M ; Giannesini B ; Mille-Hamard L ; Relizani K ; Denis R ; Hourde C ; Agbulut O ; Lutzkendorf S ; Arandel L ; Vignaud A ; Garcia L ; Ferry A ; Luquet S ; Billat V ; Bendahan D ; Ventura-Clapier R ; Schuelke M ; Amthor H | 2011The function of myostatin to restrict growth of the body musculature is often regarded as disadvantageous, because muscle prowess commonly associates with health and fitness.Here, we show that larger skeletal muscle that developed in absence of [...]Article
Our aim is to understand how skeletal muscle form and grow during vertebrate embryonic development. The early skeletal muscle (the primary myotome, composed of mononucleated, post-mitotic muscle fibers, the myocytes) is formed from the generatio[...]Article
There are clinical, neurophysiological, neuropsychological and neuroimaging evidences of brain dysfunctions in DM1 (see Meola et al., 2007 for a review). Hypotheses of developmental abnormalities in the congenital form and neurodegenerative chan[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Makri S ; Salhi S ; Richard P ; Terki N ; Romero NB ; Guicheney P ; Kaci-Ahmed MA | 2011Introduction. Mutations in the FKRP gene result in a wide spectrum of clinical conditions ranging from of congenital muscular dystophy (MDC1C) to a milder form of limb girdle muscular dystrophy (LGMD2I). Both intelligence and brain imaging have [...]Reco PNDS
Article
Myotonic dystrophy type 2 (DM2) and related disorders Report of the 180th ENMC Workshop including guidelines on diagnostics and management (3-5 December 2010; Naarden, The Netherlands) ; Udd B ; Meola G ; Krahe R ; Wansink DG ; Bassez G ; Kress W ; Schoser B ; Moxley R | 2011Accès au résumé PubMed / to PubMed abstract 13/10/2011 - Le 180e séminaire organisé par l’ENMC a porté sur la dystrophie myotonique de type 2 En décembre 2010, s’est déroulé le 5e séminaire organisé par l’ENMC, à Naarden (Pays-Bas[...]Article
Leung DG ; Germain-Lee EL ; Denger BE ; Wagner KR | 2011Accès au résumé PubMed / to PubMed abstractArticle
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Bucher T ; Joussemet B ; Astord S ; Briot-Nivard D ; Wakeling E ; Fyfe J ; Costiou P ; Marais T ; Hogrel JY ; Voit T ; Moullier P ; Barkats M | 2011Domestic cats exhibiting a recessive form of lower motor neuron (MN) degeneration, associated with a deletion of the lix1 gene, represent a large animal model of type III spinal muscular atrophy (SMA). In this study, we first analyzed the effici[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Cluet D ; Dibenedetto S ; Drouin E ; Spichty M ; Yu LL ; Thomas JL ; Gangloff YG ; Yuan CG ; Schaeffer L ; Zoli M ; Rudkin B ; Zhang Q ; Ding S | 2011One of the most important and time-consuming challenge in vivo studies of neuro-muscular diseases is to precisely monitor subtle and significant modifications of thecharacteristics within the myofiber population. To date, counting and shape desc[...]Article
Duque S ; Dominguez E ; Besse A ; Roda M ; Astord S ; Marais T ; Carcenac R ; Jacob A ; Gonzalez-Iribarren L ; Barkats M | AFM-TELETHON | 2011Intravenous (IV) delivery of self-complementary AAV9 (scAAV9) has been reported to be highly efficient for CNS gene transfer due to effective crossing of the bloodbrain- barrier (BBB). We and others recently showed that a single IV injection of [...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Carole V ; Pascal R ; Bérard C | 2011Author:C. Vuillerot1, P. Rippert1, C. Brd1 and the NM-Score study group21 L'Escale, HFME, HCL, France2 France (Angers, Grenoble, Hendaye, Lille, Marseille, Montpellier, Nice, Paris, St Denis de la Rion, St Etienne, Toulouse, Vandoeuvre les Nancy[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Dangelo MG ; Gandossini S ; Sciorati C ; Bonato S ; Brighina E ; Boneschi FM ; Comi GP ; Turconi AC ; Brunelli S ; Baldelli S ; Cattaneo D ; Bresolin N ; Clementi E | 2011ObjectiveWe performed a pilot study with the primary aim to establish the safety, tolerability of a combination of the NO donor isosorbide dinitrate and the non steroid antiinflammatorydrug ibuprofen in a cohort of adult patients affected by mus[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Billiet L ; Gonçalves C ; Berchel M ; Jaffrès PA ; Montier T ; Lehn P ; Bertrand E ; El-Ghoul Y ; Cheradame H ; Guegan P ; Pichon C ; Midoux P | 2011Duchenne muscular dystrophy (DMD) is one of the most severe myopathies caused by mutations in the dystrophin gene. Gene therapy is being investigated to introduce by non viral vectors, the normal dystrophin gene into skeletal muscle cells. The k[...]Livre
Les perspectives de vie et de mort sont renouvelées par les avancées de la médecine et par les compétences accrues des services hospitaliers. Comment les possibilités désormais ouvertes et offertes aux patients transforment-elles ou infléchis[...]