Mots-clés
> THESAURUS MYOBASE > MOTS OUTILS > 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 (3070)
| Mettre toutes les notices dans le panier | Faire une suggestion | Ajouter un critère de recherche
Etendre la recherche sur niveau(x) vers le bas
Article
Toussaint A ; Beugnet C ; De Barace C ; Toutain A ; Raynaud M ; Marcorelles P ; Pasquier L ; Chauvel-Lebreton J ; Benyaou R ; France L ; Chelly J ; Desguerre I | 2011Aim: to define molecular basis underlying different clinical phenotypes and of symptomatic DMD carriers at pediatric age.Methods: 26 cases of early symptomatic DMDcarriers followed in the french neuromuscular network were investigated. We report[...]Article
Early left ventricular dysfunction revealed in GRMD dogs bypost-processing of cine flash NMR imaging
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Gilles R ; Thibaud JL ; Toussaint M ; Blot S ; Carlier PG | 2011Background. Duchenne muscular dystrophy (DMD) due to dystrophin deficiency leads to death by heart failure in nearly 30% of cases. An early detection of myocardial abnormalities in these patients would help in the optimization of their managemen[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Nicolas A ; Lucchetti-Miganeh C ; Barloy-Hubler F ; Le Rumeur E | 2011Dystrophin, encoded by the largest DMD human gene, is a sarcolemmal protein that is ubiquiterious and found predominantly in muscle and nervous cells. Dystrophin iscomposed of 3685 residues and is constituted by various structural regions. The l[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Krasilnikova J ; Telysheva G ; Dizhbite T ; Bikovens O ; Sheibak V ; Ostrovskaja O ; Hulten L | 2011Myopathology has dysmetabolic and inflammatory disorders in pathogeneses incl. toxic cardiomyophathy and cardiomyophathy in the case of patients obesity. Plant originated products remain today an undiminished source of new pharmaceuticals. For t[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; lionel T ; Martin M ; Cornille K ; Leibovitch S ; Charles V ; Resina S ; Maurel JC | 2011Over the last decade, the significant advances made in the understanding of the molecular mechanisms responsible for debilitating muscle loss lead us to envision new pharmaceutical approaches suitable for in vivo inhibition of putative therapeut[...]Article
Le Bihan MC ; Le Bihan MC ; Bigot A ; Rogowska-Wrzesinska A ; Jensen SS ; Laine J ; Baraibar M ; Friguet B ; Dennis JL ; Jensen ON ; Coulton GR ; Mouly V | AFM-TELETHON | 2011With age, there is a gradual decline in the effectiveness of the regenerative response of skeletal muscle to damage which is accompanied by tissue remodeling such as muscle fiber atrophy, fibrosis and a general loss of muscle mass and function. [...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Vallejo Illarramendi A ; Toral I ; Ferron P ; Miranda JI ; Aizpurua JM ; Alberdi E ; Matute C ; Pastoriza N ; Lopez de Munain Arregui A | 2011Muscular dystrophies are characterized by the primary wasting of skeletal muscle, which compromises patient mobility and can lead to a complete paralysis and premature death. These diseases are among the most difficult to treat, since current ph[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Dorchies O ; Gallo C ; Reutenauer-Patte J ; Ismail HM ; Gayi E ; Petermann O ; Patthey-Vuadens O | 2011Duchenne muscular dystrophy (DMD) is a fatal muscle disorder caused by the absence of dystrophin and characterized by progressive muscle wasting. Oxidative stress and excessive calcium influx are thought to contribute to the pathogenesis. Indeed[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Pigozzo S ; Agostini J ; Wilton S ; Fletcher S ; Vitiello L | 2011Duchenne and Becker muscular dystrophy (DMD, BMD) are caused by mutations in the dystrophin gene. In general, DMD mutations disrupt the reading frame and leadto prematurely aborted dystrophin synthesis; conversely, mutations that leave the readi[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Fritah A ; Steel JH ; Nichol D ; Parker N ; Williams S ; Price A ; Strauss L ; Ryder TA ; Mobberley MA ; Poutanen M ; Parker M ; White R | AFM-TELETHON | 2011The contractile function of the heart in early postnatal development and in adult is fuelled by ATP generated mainly from fatty acid oxidation in mitochondria. Because the heart has a limited capacity to store or synthesize fatty acids, cellular[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Catelain C ; Riveron S ; Mougenot N ; Jacquet A ; Papadopoulos A ; Vauchez K ; Bonne G ; Fiszman M ; Vilquin JT | AFM-TELETHON | 2011Cardiac cell replacement has emerged as a potent new therapy by regenerating irreversibly damaged heart areas in the setting of heart failure. Cell therapy approaches have been extensively developed in the indication of ischemic infarction, but [...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Bugiardini E ; Passeri E ; Sansone V ; Ambrosi B ; Corbetta S ; Renna LV ; Cardani R ; Meola G | 2011DM1 and DM2 are progressive multisystem genetic disorders that share a similar pathogenetic mechanism and clinical manifestations. The endocrine features include insulin resistance and testicular failure. Some clinical studies showed how hypogon[...]Article
AFM-TELETHON 2011For most tissues, stem cell numbers decline negligibly with age, but there is a nevertheless an age-dependent decline in stem cell functionality. Many molecular, biochemical, and functional features of stem cells have been characterized across a[...]Article
IXèmes Journées Annuelles de la Société française de Myologie (SFM) (3-5 novembre 2011; Angers) ; Marie J | 2011La dystrophie myotonique de type 1 (DM1) est la pathologie musculaire la plus fréquente chez l'adulte. C'est une pathologie autosomale dominante à caractère multisystémique touchant de nombreux organes. La mutation est une expansion anormale du [...]Article
Purpose: Inclusion Body Myositis (IBM) is the most common acquired myopathy in patients above the age of 50 years. This disabling disease is an inflammatory myopathy characterized by CD8+ cytotoxic infiltrates and amyloid deposits. IBM remains r[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Skuk D | 2011Acute rejection of myofibers expressing alloantigens in nonhuman primates in which immunosuppression is not adequate is mainly driven by CD8+ and CD4+ lymphocytesthat focally accumulate to surround and invade these myofibers, which appear non-ne[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Charbonnier F ; Branchu J ; Biondi O ; Deforges S ; Sanchez G ; Coté J ; Chanoine C ; Lopes P ; Pariset P ; Lancelin C | 2011Spinal Muscular Atrophy (SMA), a lethal neurodegenerative disease which occurs in childhood, is due to the misexpression of the survival-motor-neuron (SMN) proteinin motor-neurons. We have evaluated the effect of a running-based training (Gronda[...]Article
RNA therapeutic approaches have proven to be very successful in cell culture and in animal experiments. Some oligonucleotides based clinical trials are currently already in progress. To be efficient, the oligonucleotides must be composed of non-[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Gaëlle R ; Allard B | 2011In skeletal muscle, contraction is induced by a massive release of calcium from the sarcoplasmic reticulum (SR) in response to depolarization of the cell. Duringsustained depolarization, a voltage-activated calcium influx is also known to occur [...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Jansen M ; de Jong M ; van Alfen N ; De Groot I | 2011Background: Clinically relevant outcome measures are necessary to monitor disease progression and to evaluate treatments in boys with Duchenne Muscular Dystrophy(DMD). Endurance is related to functioning in daily life and is, therefore, a clinic[...]Article
Mouly V ; Larghero J ; Toy-Miou M ; Eymard B ; Pascal L ; Chapon F ; Butler Browne G ; Lacau Saint Guily J | AFM-TELETHON | 2011Degenerative dystrophy of the pharyngeal muscles in OPMD causes fibrosis with swallowing disorders and a decreased relaxation of the cricopharyngeal muscle (CPM) (muscle of the upper esophageal sphincter, UES). The myotomy of the UES improves on[...]Article
Le Guiner C ; Montus M ; Garcia L ; Y.Fromes ; Hogrel JY ; Carlier P ; Cherel Y ; Moullier P | AFM-TELETHON | 2011In Duchenne Muscular Dystrophy (DMD) the selective removal by exon skipping of exons flanking an out-of frame mutation in the dystrophin messenger can result in in-frame mRNA transcripts that are translated into shorter but functionally active d[...]Article
IXèmes Journées Annuelles de la Société française de Myologie (SFM) (3-5 novembre 2011; Angers) ; Heron D ; Jacquette A ; Whalen S ; Angeard N ; Eymard B | 2011La dystrophie myotonique de type 1 (DM1) est une maladie neuro-musculaire autosomique dominante d'une grande variabilité phénotypique, liée à une expansion instable d'un triplet CTG dans la région 3' du gène DMPK L'instabilité méiotique de l'exp[...]Article
4th International Congress of Myology, 4ème colloque international de Myologie (9-13 mai 2011; Lille (France)) ; Ben Yaou R ; Demay L ; Chikhaoui K ; Hamroun D ; Beroud C ; Richard P ; Bonne G | 2011In 1999, we reported the first LMNA gene mutations responsible for the autosomal forms of Emery-Dreifuss muscular dystrophy (EDMD), this gene encoding nuclear envelope proteins, the lamins A/C. Since then, a huge number of patients carrying LMNA[...]