Zobrazeno 1 - 10
of 83
pro vyhledávání: '"J M Lupoglazoff"'
Autor:
I. Denjoy, J.-M. Lupoglazoff
Publikováno v:
EMC - Cardiologie. 1:1-8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea9c957e56b82201af081e6c83e79412
https://doi.org/10.1016/s1166-4568(06)39431-4
https://doi.org/10.1016/s1166-4568(06)39431-4
Autor:
Pascale Guicheney, J. Kamblock, Marielle Alders, Aam Wilde, Alex V. Postma, Marcel M.A.M. Mannens, Guy Vaksmann, J. M. Lupoglazoff, Isabelle Denjoy, L. Dubosq-Bidot, P. Sebillon
Publikováno v:
Journal of Medical Genetics, 42(11), 863-870. BMJ Publishing Group
Journal of medical genetics, 42(11), 863-870. BMJ Publishing Group
Journal of medical genetics, 42(11), 863-870. BMJ Publishing Group
Background: The aim of the study was to assess underlying genetic cause(s), clinical features, and response to therapy in catecholaminergic polymorphic ventricular tachycardia (CPVT) probands. Methods and results: We identified 13 missense mutations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48bbfb7d883b7d4045685a31da4b25a8
https://hdl.handle.net/11245/1.247230
https://hdl.handle.net/11245/1.247230
Autor:
J.-M. Lupoglazoff, I. Denjoy
Publikováno v:
Archives de Pédiatrie. 11:1268-1273
Arrhythmias in neonates and infants require a specific management due to the particular nature of the rhythm anomalies in children. Accurate diagnosis of the tachycardia is realised mainly by means of ECG recording and vagal manoeuvres. The nature of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac2b31c2dfe0b8f6acb225b327a703c1
https://doi.org/10.1016/j.arcped.2004.02.010
https://doi.org/10.1016/j.arcped.2004.02.010
Publikováno v:
Archives de Pédiatrie. 9:1256-1259
Resume Introduction. – Les etudes recentes concernant les dysfonctionnements des canaux ioniques (channelopathies) permettent d’expliquer bon nombre d’arythmies ventriculaires graves considerees autrefois comme primitives. Observation. – Un c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dd7f8c60307c2460c9980d244ced7e73
https://doi.org/10.1016/s0929-693x(02)00124-0
https://doi.org/10.1016/s0929-693x(02)00124-0
Publikováno v:
Archives de Pédiatrie. 8:525-534
Resume Le syndrome du QT long congenital (SQTL) est caracterise par un allongement de lˈintervalle QT sur lˈelectrocardiogramme (ECG). Cliniquement et genetiquement heterogene, il est associe a un risque de troubles du rythme ventriculaire graves (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1755ce0de3682db9e724d96392afb804
https://doi.org/10.1016/s0929-693x(00)00261-x
https://doi.org/10.1016/s0929-693x(00)00261-x
Autor:
Guy Vaksmann, G. Maillard, Didier Klug, P. Richard, J. M. Lupoglazoff, Philippe Coumel, Isabelle Denjoy, Myriam Berthet, Pascale Guicheney, Antoine Leenhardt, Nathalie Neyroud, Bernard Hainque, L. Demay
Publikováno v:
Scopus-Elsevier
Background —The 2 genes KCNQ1 (LQT1) and HERG (LQT2), encoding cardiac potassium channels, are the most common cause of the dominant long-QT syndrome (LQTS). In addition to QT-interval prolongation, notched T waves have been proposed as a phenotypi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6274755eb19f964bbf5ed3e81a59805f
https://doi.org/10.1161/01.cir.103.8.1095
https://doi.org/10.1161/01.cir.103.8.1095
Publikováno v:
Prenatal Diagnosis. 19:767-770
Junctional ectopic tachycardia (JET) is a rare cardiac arrhythmia characterized by atrio-ventricular dissociation, a high rate junctional escape rhythm and poor clinical tolerance in neonates and infants. Sudden infant death has been reported. The in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::77e91943da2bcc6827310065b62178c5
https://doi.org/10.1002/(sici)1097-0223(199908)19:8<767::aid-pd617>3.0.co
https://doi.org/10.1002/(sici)1097-0223(199908)19:8<767::aid-pd617>3.0.co
Autor:
Isabelle Denjoy, Craig T. January, Véronique Fressart, Rachel Peat, Pascale Guicheney, Sabine Duchatelet, Daniel C. Bartos, J. M. Lupoglazoff, Michael J. Ackerman, Brian P. Delisle, Myriam Berthet, Didier Klug, Don E. Burgess
Background Loss-of-function mutations in the gene KCNQ1 encoding the Kv7.1 K + channel cause long QT syndrome type 1 (LQT1), whereas gain-of-function mutations are associated with short QT syndrome as well as familial atrial fibrillation (FAF). Howev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a53ad77704ec7cb2556434111889a55
https://europepmc.org/articles/PMC3706092/
https://europepmc.org/articles/PMC3706092/
Autor:
I. Denjoy, Jean-Christophe Mercier, E. Lejay, Catherine Delanoë, J.-M. Lupoglazoff, Stéphane Auvin, Luigi Titomanlio
Publikováno v:
Neurology. 74(15)
A 4-year-old girl was seen in the pediatric emergency department because of a first generalized tonic-clonic seizure that occurred at school. The seizure was preceded by a sudden, prolonged attack of unconsciousness, lasted 5 minutes, and was followe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::44264f2b161332c07bcae04c091531a2
https://pubmed.ncbi.nlm.nih.gov/20385884
https://pubmed.ncbi.nlm.nih.gov/20385884
Autor:
J-M, Lupoglazoff, I, Denjoy
Publikováno v:
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie. 11(10)
Arrhythmias in neonates and infants require a specific management due to the particular nature of the rhythm anomalies in children. Accurate diagnosis of the tachycardia is realised mainly by means of ECG recording and vagal manoeuvres. The nature of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e6b87267d1318d9c9307d6bea1ea3236
https://pubmed.ncbi.nlm.nih.gov/15475291
https://pubmed.ncbi.nlm.nih.gov/15475291