Détail du congrès:
Congrès: Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) (26-30 mai 2008)
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Documents disponibles provenant de ce congrès (565)
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Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Duddy W ; Cohen T ; Partridge T | 2008Loss of muscle mass through atrophy is associated with aging, cachexia, inactivity through illness or injury, and many neuromuscular disorders. Regulation of muscle mass is important for strength and fitness of healthy individuals. Change in mus[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Pallafacchina G ; Montarras D ; Cumano A ; Buckingham M | 2008Satellite cells are the main progenitor cells for skeletal muscle growth and regeneration under physiological conditions. The difficulty of purifying these quiescent cells in sufficient number has precluded their biochemical characterization. Pa[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Pautrel I ; Crapie C ; Jacques D ; Sequestra N ; Noguiez-Hellin P | 2008Généthon’s ETGC is working in 5 production rooms - dispatched on two sites - among which 3 are dedicated to viral vectors production for development of therapeutic products for phase I and II clinical trials. These productions are performed in c[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Burghes A ; Workman E ; McGovern V ; Saieva L ; Pellizzoni L ; Beattie C | 2008Spinal muscular atrophy is caused by loss or mutation of the SMN1 gene and retention of SMN2, leading to low levels of functional SMN. A major function of SMN is assembly of the heptameric Sm ring onto snRNA with SMA tissues having reduced activ[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Junion G ; Bataillé L ; Jagla T ; Da Ponte JP ; Tapin R ; Jagla K | 2008Correct diversification of cell types during development is controlled by combinatorial code of transcription factor activities, the identity gene code. The role of identity genes in specifying cell fates has been demonstrated in a broad range o[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Gueneau L ; Ben Yaou R ; Demay L ; Llense S ; Chikhaoui K ; Trabelsi M ; Beugnet C ; Deburgrave N ; Leturcq F ; Chelly J ; Richard P ; Bonne G | 2008Emery-Dreifuss Muscular Dystrophy (EDMD) is a rare autosomal or X-linked recessive condition, associating muscular dystrophy, joint contractures and cardiac disease. Mutations in 2 genes, EMD (emerin) and LMNA (Lamins A/C) encoding nuclear envel[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Arvanitis DA ; Sanoudou D ; Kolokathis F ; Vafiadaki E ; Theodorakis G ; Kontrogianni-Konstantopoulos A ; Paraskevaidis IA ; Adamopoulos S ; Dorn II GU ; Kremastinos DTH ; Kranias EG | 2008Abnormal Ca-cycling in the cardiomyocyte is a hallmark of dilated cardiomyopathy (DCM). Furthermore, DCM patients are at substantial risk for sudden cardiac death due to malignant ventricular arrhythmias. The histidine-rich calcium binding prote[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Apostol P ; Cimponeriu D ; Toma M ; Butoianu N ; Burloiu C ; Craiu D ; Magureanu S ; Gavrila L | 2008Vitamin D is a steroid hormone known for its key roles in calcium homeostasis, proliferation and apoptosis. Previous studies have also reported the association of vitamin D deficiency with muscle weakness and neuromuscular dysfunction. The vitam[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Melki J | 2008Motor neuron diseases (MND) are rare diseases characterized by degeneration of lower (spinal muscular atrophy, SMA), upper (spastic paraplegia, HSP and primary lateral sclerosis) or both upper and lower motor neurons (amyotrophic lateral scleros[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Basak AN | 2008ALS is the most common adult-onset motor neuron disease. Described in 1869, by the French Neurobiologist J. M. Charcot, the primary disease hallmark is the selective and progressive degeneration of the neurons in the corticospinal tracts. ALS pr[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Laing NG | 2008The congenital myopathies are a diverse group of entities, with considerable genetic heterogeneity. The genetic heterogeneity includes mutations in multiple different genes causing similar pathological phenotypes, and multiple different patholog[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Makri S ; Clarke NF ; Richard P ; Maugenre S ; Demay L ; Terki N ; Bonne G ; Guicheney P | 2008Background: Mutation p.Arg527Pro in the lamin A/C, encoded by LMNA gene, was identified several times in dominant Emery-Dreifuss muscular dystrophy and cases with muscular dystrophy, lipodystrophy, and cardiac rhythm disturbances. We found this [...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Musarella M ; Bellouze S ; Caillol G ; Autillo-Touati A | 2008Mouse mutants provide good models for the study of degenerative neuromuscular diseases in human. Although recent data indicate a pivotal role for Terminal Schwann Cells (TSC) in maintaining synaptic structure and function, their role in patholog[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Huynh M ; Garcia-Filipe S ; Morin C ; Barbier-Chassefière V ; Besse S ; Narassimprakash H ; Jeniskens G ; Martelly I ; Papy-Garcia D | 2008Despite the increasing evidences demonstrating the diverse roles of glycosaminoglycans (GAGs) in many fundamental biological processes, most studies directed to understand the extracellular matrix implication in cardiac dysfunction focuses mainl[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Fauchille S ; Adin P ; Barnay-Toutain F ; Burie C ; Dufour D ; Halbout C ; Le Provost G ; Maleau G ; Sander B ; Noguiez-Hellin P | 2008Genethon has been provided with GMP manufacturing facilities of about 600 m2 for the production of viral vectors for human gene therapy trials. All steps are performed on the site: plasmid production, cell banking, cell culture, purification and[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Moore-Morris T ; Varrault A ; Le Digarcher A ; Journot L ; Nargeot J ; Couette B | 2008Maintaining or even enhancing skeletal muscle mass is critical not only in inherited muscular disorders but also in the context of aging and in various disease states associated with muscle loss. The aim of any treatment for muscle wasting is to[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Larue S ; Maisonobe T ; Papo T ; Chapelon-Abric C ; Lidove O ; Servan J ; Veber H ; Dashi F ; Dubourg O | 2008We report four patients with chronic myopathy suggestive of inclusion body myositis (IBM), but in whom muscle biopsy showed a granulomatous myositis (GM). Our 4 patients, three women and one men, aged 71 to 83, presented with a slowly progressiv[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Dorchies O ; Comyn S ; Ruegg U | 2008Muscular dystrophies are characterized by fibrosis, a process leading to abnormal accumulation of materials of fibroblastic origin in the skeletal muscles as necrosis-regeneration cycles take place. Fibrosis results from alterations in a multifa[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Maier A ; Cohen R ; Blom J ; Westendorp R | 2008Sarcopenia is defined as a decrease in skeletal muscle mass that is particularly caused by satellite cells being unable to proliferate. The number of satellite cells, as well as the proliferative capacity of isolated satellite cells in vitro dec[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Renou L ; Stora S ; Ben Yaou R ; Sinkovec M ; Demay L ; Richard P ; Peterlin B ; Bonne G | 2008Heart-hand syndrome (HHS) is a heterogeneous group of genetic disorders characterized by congenital cardiac and limb deformities. Five subtypes are currently reported, among them the Slovenian type (HHS-S) associating bracydactyly and cardiac co[...]Article
Heat shock treatment increases engraftment of human transplanted myoblasts into immunodeficient mice
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Bencze M ; Riederer I ; Negroni E ; Bigot A ; Butler-Browne GA ; Mouly V | 2008One of the phenomena known to limit the success of myoblast transfer therapy (MTT) is the massive and early cell death observed during the first few hours after cell injection. A major part of injected cells die by necrosis and apoptosis, thus d[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Martinez Perea MDC ; Liste H ; Posadas Martinez MM | 2008The mitochondrial DNA point mutation T8993G has been associated with NARP and maternally inherited Leigh syndrome (MILS). Usually there is a correlation between the percentage of mutated mtDNA and clinical severity. Objectives: The aim is to sho[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Kaneva G ; Laporte J ; Winsor B ; Friant S | 2008The human myotubularin gene (hMTM1) that is mutated in a severe congenital neuromuscular disease, X-linked myotubular myopathy (XLMTM), encodes a phosphatase specific for phosphatidylinositol 3-phosphate (PtdIns(3)P) and PtdIns(3,5)P2. In Saccha[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Abriat A ; Kozak G ; Brosset C ; Figarella-Branger D ; Monnier N ; Cozzone PJ ; Pellissier JF ; Lunardi J ; Bendahan D | 2008Exertional heat stroke (EHS) occurs in young, healthy individuals engaged in a strenuous physical activity and is accompanied by hyperthermic and lost of consciousness. Given that EHS and Malignant Hyperthermia (MH), a subclinical myopathy due t[...]Article
Congrès international de myologie 2008 (International Congress of Myology 2008; 26-30 mai 2008; Marseille, France) ; Belayew A | 2008Facioscapulohumeral muscular dystrophy (FSHD) is considered a disorder of gene regulation. The pathological deletions contract the D4Z4 repeat array in the 4q35 subtelomeric region from 11 -150 units in healthy individuals down to 1-10 units in [...]