Molecular genetics and functional anomalies in a series of 248 Brugada cases with 11 mutations in the TRPM4 channel.

Autor: Hui Liu, Stéphanie Chatel, Christophe Simard, Ninda Syam, Laurent Salle, Vincent Probst, Julie Morel, Gilles Millat, Michel Lopez, Hugues Abriel, Jean-Jacques Schott, Romain Guinamard, Patrice Bouvagnet

Publikováno v: PLoS ONE, Vol 8, Iss 1, p e54131 (2013)

Brugada syndrome (BrS) is a condition defined by ST-segment alteration in right precordial leads and a risk of sudden death. Because BrS is often associated with right bundle branch block and the TRPM4 gene is involved in conduction blocks, we screen

Externí odkaz: https://doaj.org/article/8c664dfcc2d54849bed4c4b23a727a01

Lower-limb hypopallesthesia: A risk factor for falls in cognitively intact non-diabetic older adults

Autor: Cédric Annweiler, Armelle Gentric, Julie Morel

Publikováno v: Maturitas
Maturitas, Elsevier, 2021, 143, pp.115-117. ⟨10.1016/j.maturitas.2020.10.001⟩

Peripheral neuropathies (PN) in older adults often involve altered vibrational perception, i.e. hypopallesthesia. The main objective of this cross-sectional study was to determine whether age-related lower-limb hypopallesthesia is associated with a h

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::19dc22f78368fbf34cb171d9075100a1
https://hal.archives-ouvertes.fr/hal-03492667

A Service Delivery Model for Children with DCD Based on Principles of Best Practice

Autor: Chantal Camden, France Léger, Julie Morel, Cheryl Missiuna

Publikováno v: Physical & Occupational Therapy In Pediatrics. 35:412-425

Aims. In this perspective article, we propose the Apollo model as an ex- ample of an innovative interdisciplinary, community-based service delivery model for children with Developmental Coordination Disorder (DCD) characterized by the use of graduate

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2aee564771e20006135e99c9a4c1195
https://doi.org/10.3109/01942638.2014.978932

Molecular genetics and functional anomalies in a series of 248 Brugada cases with 11 mutations in the TRPM4 channel

Autor: Jean-Jacques Schott, Laurent Sallé, Julie Morel, Hui Liu, Patrice Bouvagnet, Hugues Abriel, Christophe Simard, Michel Lopez, Vincent Probst, Ninda Syam, Gilles Millat, Stéphanie Chatel, Romain Guinamard

Publikováno v: PLoS ONE, Vol 8, Iss 1, p e54131 (2013)
PLoS ONE
Liu, Hui; Chatel, Stéphanie; Simard, Christophe; Syam, Ninda; Salle, Laurent; Probst, Vincent; Morel, Julie; Millat, Gilles; Lopez, Michel; Abriel, Hugues; Schott, Jean-Jacques; Guinamard, Romain; Bouvagnet, Patrice (2013). Molecular genetics and functional anomalies in a series of 248 Brugada cases with 11 mutations in the TRPM4 channel. PLoS ONE, 8(1), e54131. Public Library of Science 10.1371/journal.pone.0054131
PloS one

Brugada syndrome (BrS) is a condition defined by ST-segment alteration in right precordial leads and a risk of sudden death. Because BrS is often associated with right bundle branch block and the TRPM4 gene is involved in conduction blocks, we screen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::890fb2982034e107011bc16723943e84
https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23382873/pdf/?tool=EBI

Na v1.4 and Na v1.5 are modulated differently during muscle immobilization and contractile phenotype conversion

Autor: Jean-Pierre Pennec, Maxime Gioux, Raphael Leschiera, Gildas Gueret, Marie-Agnès Giroux-Metges, Fabrice Rannou, Julie Morel, Mickaël Droguet

Publikováno v: Journal of Applied Physiology
Journal of Applied Physiology, American Physiological Society, 2011, 111 (2), pp.495--507. ⟨10.1152/japplphysiol.01136.2010⟩
Journal of Applied Physiology, 2011, 111 (2), pp.495--507. ⟨10.1152/japplphysiol.01136.2010⟩

Muscle immobilization leads to modification in its fast/slow contractile phenotype. Since the properties of voltage-gated sodium channels (Nav) are different between “fast” and “slow” muscles, we studied the effects of immobilization on the c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::437c4729cee781a462ba5b981a008faf
https://hal-univ-rennes1.archives-ouvertes.fr/hal-01159465