Search Results - "Venance, L"

The non-dystrophic myotonias: molecular pathogenesis, diagnosis and treatment by Matthews, E., Fialho, D., Tan, S. V., Venance, S. L., Cannon, S. C., Sternberg, D., Fontaine, B., Amato, A. A., Barohn, R. J., Griggs, R. C., Hanna, M. G.

“…The non-dystrophic myotonias are an important group of skeletal muscle channelopathies electrophysiologically characterized by altered membrane excitability…”
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Bidirectional Activity-Dependent Plasticity at Corticostriatal Synapses by Fino, Elodie, Glowinski, Jacques, Venance, Laurent

“…Corticostriatal projections originate from the entire cerebral cortex and provide the major source of glutamatergic inputs to the basal ganglia. Despite the…”
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GABAergic circuits control spike-timing-dependent plasticity by Paille, Vincent, Fino, Elodie, Du, Kai, Morera-Herreras, Teresa, Perez, Sylvie, Kotaleski, Jeanette Hellgren, Venance, Laurent

“…The spike-timing-dependent plasticity (STDP), a synaptic learning rule for encoding learning and memory, relies on relative timing of neuronal activity on…”
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Electrical and chemical transmission between striatal GABAergic output neurones in rat brain slices by Venance, Laurent, Glowinski, Jacques, Giaume, Christian

“…Basal ganglia are interconnected subcortical nuclei, connected to the thalamus and all cortical areas involved in sensory motor control, limbic functions and…”
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Pompe Disease: Diagnosis and Management. Evidence-Based Guidelines from a Canadian Expert Panel by Tarnopolsky, Mark, Katzberg, Hans, Petrof, Basil J, Sirrs, Sandra, Sarnat, Harvey B, Myers, Kimberley, Dupré, Nicolas, Dodig, Dubravka, Genge, Angela, Venance, Shannon L, Korngut, Lawrence, Raiman, Julian, Khan, Aneal

“…Pompe disease is a lysosomal storage disorder caused by a deficiency of the enzyme acid alpha-glucosidase. Patients have skeletal muscle and respiratory…”
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Non-dystrophic myotonia: prospective study of objective and patient reported outcomes by TRIVEDI, Jaya R, BUNDY, Brian, GORHAM, Nina, HERBELIN, Laura, CANNON, Stephen, AMATO, Anthony, GRIGGS, Robert C, HANNA, Michael G, BAROHN, Richard J, STATLAND, Jeffrey, SALAJEGHEH, Mohammad, DIPA RAJA RAYAN, VENANCE, Shannon L, YUNXIA WANG, FIALHO, Doreen, MATTHEWS, Emma, CLELAND, James

“…Non-dystrophic myotonias are rare diseases caused by mutations in skeletal muscle chloride and sodium ion channels with considerable phenotypic overlap between…”
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The primary periodic paralyses: diagnosis, pathogenesis and treatment by Venance, S. L., Cannon, S. C., Fialho, D., Fontaine, B., Hanna, M. G., Ptacek, L. J., Tristani-Firouzi, M., Tawil, R., Griggs, R. C.

“…Periodic paralyses (PPs) are rare inherited channelopathies that manifest as abnormal, often potassium (K)-sensitive, muscle membrane excitability leading to…”
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Presynaptic adenosine A 2A receptors dampen cannabinoid CB 1 receptor‐mediated inhibition of corticostriatal glutamatergic transmission by Ferreira, S G, Gonçalves, F Q, Marques, J M, Tomé, Â R, Rodrigues, R J, Nunes‐Correia, I, Ledent, C, Harkany, T, Venance, L, Cunha, R A, Köfalvi, A

“…Background and Purpose Both cannabinoid CB 1 and adenosine A 2A receptors ( CB 1 receptors and A 2A receptors) control synaptic transmission at corticostriatal…”
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Common epigenetic changes of D4Z4 in contraction-dependent and contraction-independent FSHD by de Greef, Jessica C, Lemmers, Richard J.L.F, van Engelen, Baziel G.M, Sacconi, Sabrina, Venance, Shannon L, Frants, Rune R, Tawil, Rabi, van der Maarel, Silvère M

“…Facioscapulohumeral muscular dystrophy (FSHD), caused by partial deletion of the D4Z4 macrosatellite repeat on chromosome 4q, has a complex genetic and…”
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Clinical features of facioscapulohumeral muscular dystrophy 2 by DE GREEF, J. C, LEMMERS, R. J. L. F, DESNUELLE, C, SPULER, S, TARNOPOLSKY, M, VENANCE, S. L, FRANTS, R. R, VAN DER MAAREL, S. M, TAWIL, R, CAMANO, P, DAY, J. W, SACCONI, S, DUNAND, M, VAN ENGELEN, B. G. M, KIURU-ENARI, S, PADBERG, G. W, ROSA, A. L

“…In some 5% of patients with facioscapulohumeral muscular dystrophy (FSHD), no D4Z4 repeat contraction on chromosome 4q35 is observed. Such patients, termed…”
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Archetypes of incomplete stories in chronic illness medical encounters by Koopman, Wilma J., LaDonna, KA, Kinsella, EA, Venance, SL, Watling, CJ

“…During encounters, patients and practitioners engage in conversations to address health concerns. Because these interactions are time-pressured events, it may…”
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Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy by Osborne, R J, Welle, S, Venance, S L, Thornton, C A, Tawil, R

“…Facioscapulohumeral muscular dystrophy (FSHD) is caused by deletions within a tandem array of D4Z4 repeats on chromosome 4q35. In addition to muscle…”
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Gap junctions and connexin expression in the normal and pathological central nervous system by Rouach, N, Avignone, E, Même, W, Koulakoff, A, Venance, L, Blomstrand, F, Giaume, C

“…Gap junctions are widely expressed in the various cell types of the central nervous system. These specialized membrane intercellular junctions provide the…”
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Deletion of Maged1 in mice abolishes locomotor and reinforcing effects of cocaine by De Backer, Jean‐François, Monlezun, Stéphanie, Detraux, Bérangère, Gazan, Adeline, Vanopdenbosch, Laura, Cheron, Julian, Cannazza, Giuseppe, Valverde, Sébastien, Cantacorps, Lídia, Nassar, Mérie, Venance, Laurent, Valverde, Olga, Faure, Philippe, Zoli, Michele, De Backer, Olivier, Gall, David, Schiffmann, Serge N, de Kerchove d'Exaerde, Alban

“…Melanoma antigen genes (Mage) were first described as tumour markers. However, some of Mage are also expressed in healthy cells where their functions remain…”
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Intercellular calcium signaling and gap junctional communication in astrocytes by Giaume, Christian, Venance, Laurent

“…Two main characteristics of astrocytes are their elaborated intracellular calcium signaling and their high degree of intercellular communication mediated by…”
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Endothelins regulate astrocyte gap junctions in rat hippocampal slices by Blomstrand, F., Venance, L., Sirén, A.-L., Ezan, P., Hanse, E., Glowinski, J., Ehrenreich, H., Giaume, C.

“…Gap junctional communication (GJC) is a typical feature of astrocytes proposed to contribute to the role played by these glial cells in brain physiology and…”
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Spike frequency adaptation is developmentally regulated in substantia nigra pars compacta dopaminergic neurons by Vandecasteele, M, Deniau, J.-M, Venance, L

“…Abstract Dopaminergic neurons of the substantia nigra pars compacta play a key role in the modulation of basal ganglia and provide a reward-related teaching…”
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Preservation of the hyperdirect pathway of basal ganglia in a rodent brain slice by Bosch, C, Mailly, P, Degos, B, Deniau, J.-M, Venance, L

“…Highlights ► We established a rat brain slice preserving the hyperdirect pathway of basal ganglia. ► We analyzed transmission and short-term plasticity in the…”
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Asymmetric spike-timing dependent plasticity of striatal nitric oxide-synthase interneurons by Fino, E, Paille, V, Deniau, J.-M, Venance, L

“…Abstract Corticostriatal projections constitute the major inputs to basal ganglia, an ensemble of sub-cortical nuclei involved in the learning of…”
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Presynaptic adenosine A2A receptors dampen cannabinoid CB1 receptor‐mediated inhibition of corticostriatal glutamatergic transmission by Ferreira, S G, Gonçalves, F Q, Marques, J M, Tomé, Â R, Rodrigues, R J, Nunes‐Correia, I, Ledent, C, Harkany, T, Venance, L, Cunha, R A, Köfalvi, A

“…Background and Purpose Both cannabinoid CB1 and adenosine A2A receptors (CB1 receptors and A2A receptors) control synaptic transmission at corticostriatal…”
Get full text