I Denjoy
Overview
Explore the profile of I Denjoy including associated specialties, affiliations and a list of published articles.
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Articles
78
Citations
1596
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0
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Recent Articles
1.
Extramiana F, Milleron O, Elbitar S, Uccellini A, Langeois M, Spentchian M, et al.
Sci Rep
. 2018 Aug;
8(1):13019.
PMID: 30158670
Mutations in the TGFβR2 gene have been associated with a life threatening risk of aortic dissection but no arrhythmic death has been previously reported. Two young females carrying a TGFβR2...
2.
Kaltenbach S, Capri Y, Rossignol S, Denjoy I, Soudee S, Aboura A, et al.
Clin Genet
. 2012 Oct;
84(1):78-81.
PMID: 23061425
We report a child with Beckwith-Wiedemann syndrome (BWS) as the consequence of an apparently balanced, maternally inherited reciprocal translocation t(11;17)(p15.5;q21.3). His mother and aunt, who inherited the translocation from their...
3.
Auvin S, Lejay E, Delanoe C, Denjoy I, Lupoglazoff J, Mercier J, et al.
Neurology
. 2010 Apr;
74(15):e61-4.
PMID: 20385884
No abstract available.
4.
Mabo P, Leenhardt A, Jaillon P, Kacet S, Aubin F, Denjoy I, et al.
Ann Cardiol Angeiol (Paris)
. 2009 May;
58(3):151-8.
PMID: 19477433
Objectives: To describe the management of patients with atrial fibrillation (AF) and to study consistency with guidelines on management of AF. Patients And Methods: Observational study on a random sample...
5.
Denjoy I, Lupoglazoff J, Guicheney P, Leenhardt A
Arch Cardiovasc Dis
. 2008 Apr;
101(2):121-5.
PMID: 18398397
Sudden death (SD) in childhood is rare, representing only 10% of paediatric mortality after one year of age. The individual risk is estimated between 1 in 20.000 and 1 in...
6.
Denjoy I, Lupoglazoff J, Villain E, Vaksmann G, Godart F, Lucet V, et al.
Arch Mal Coeur Vaiss
. 2007 Jul;
100(5):359-64.
PMID: 17646758
Unlabelled: Data on the Jervell and Lange-Nielsen syndrome (JLN), the long QT syndrome (LQTS) variant associated with deafness and caused by homozygous or compound heterozygous mutations on the KCNQ1 or...
7.
Postma A, Denjoy I, Kamblock J, Alders M, Lupoglazoff J, Vaksmann G, et al.
J Med Genet
. 2005 Nov;
42(11):863-70.
PMID: 16272262
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...
8.
Lucet V, Do Ngoc D, Denjoy I
Arch Pediatr
. 2005 Oct;
12(12):1709-13.
PMID: 16214311
Introduction: In case of an accessory pathway, children are exposed to severe cardiac events including sudden death. Radiofrequency ablation is a standardized procedure, which can be applied to a significant...
9.
Denjoy I, Postma A, Lupoglazoff J, Vaksman G, Kamblock J, Leenhardt A, et al.
Arch Mal Coeur Vaiss
. 2005 Jun;
98(5):506-12.
PMID: 15966600
Catecholinergic ventricular tachycardia is an adrenergic induced polymorphic ventricular arrhythmia. It occurs in infancy and is responsible for syncope and sudden death in the absence of any morphological cardiac abnormality....
10.
Vaksmann G, DHoinne C, Lucet V, Guillaumont S, Lupoglazoff J, Chantepie A, et al.
Heart
. 2005 Apr;
92(1):101-4.
PMID: 15831598
Objectives: To investigate the clinical profile, natural history, and optimal management of persistent or permanent junctional reciprocating tachycardia (PJRT) in children. Methods And Results: 85 patients meeting the ECG criteria...