Schott JJ - Search Results

1

Multimodality imaging and transcriptomics to phenotype mitral valve dystrophy in a unique knock-in Filamin-A rat model.

Delwarde C, Toquet C, Aumond P, Kayvanjoo AH, Foucal A, Le Vely B, Baudic M, Lauzier B, Blandin S, Véziers J, Paul-Gilloteaux P, Lecointe S, Baron E, Massaiu I, Poggio P, Rémy S, Anegon I, Le Marec H, Monassier L, Schott JJ, Mass E, Barc J, Le Tourneau T, Merot J, Capoulade R. Delwarde C, et al. Among authors: schott jj. Cardiovasc Res. 2023 May 2;119(3):759-771. doi: 10.1093/cvr/cvac136. Cardiovasc Res. 2023. PMID: 36001550

2

[Hereditary cardiac arrhythmia].

Le Marec H, Schott JJ. Le Marec H, et al. Among authors: schott jj. Arch Mal Coeur Vaiss. 1997 Apr;90 Spec No 1:57-66. Arch Mal Coeur Vaiss. 1997. PMID: 9238458 Review. French.

3

[Congenital long QT syndromes].

Le Marec H, Schott JJ. Le Marec H, et al. Among authors: schott jj. Arch Mal Coeur Vaiss. 1997 Jun;90 Spec No 3:25-35. Arch Mal Coeur Vaiss. 1997. PMID: 9295920 French.

4

Clinical characteristics of a familial inherited myxomatous valvular dystrophy mapped to Xq28.

Trochu JN, Kyndt F, Schott JJ, Gueffet JP, Probst V, Bénichou B, Le Marec H. Trochu JN, et al. Among authors: schott jj. J Am Coll Cardiol. 2000 Jun;35(7):1890-7. doi: 10.1016/s0735-1097(00)00617-3. J Am Coll Cardiol. 2000. PMID: 10841240 Free article.

5

Haploinsufficiency in combination with aging causes SCN5A-linked hereditary Lenègre disease.

Probst V, Kyndt F, Potet F, Trochu JN, Mialet G, Demolombe S, Schott JJ, Baró I, Escande D, Le Marec H. Probst V, et al. Among authors: schott jj. J Am Coll Cardiol. 2003 Feb 19;41(4):643-52. doi: 10.1016/s0735-1097(02)02864-4. J Am Coll Cardiol. 2003. PMID: 12598077 Free article.

6

Cosegregation of the Marfan syndrome and the long QT syndrome in the same family leads to a severe cardiac phenotype.

Probst V, Allouis M, Kyndt F, Lande G, Trochu JN, Schott JJ, Le Marec H. Probst V, et al. Among authors: schott jj. Am J Cardiol. 2003 Mar 1;91(5):635-7. doi: 10.1016/s0002-9149(02)03329-5. Am J Cardiol. 2003. PMID: 12615283 No abstract available.

7

Novel brugada SCN5A mutation leading to ST segment elevation in the inferior or the right precordial leads.

Potet F, Mabo P, Le Coq G, Probst V, Schott JJ, Airaud F, Guihard G, Daubert JC, Escande D, Le Marec H. Potet F, et al. Among authors: schott jj. J Cardiovasc Electrophysiol. 2003 Feb;14(2):200-3. doi: 10.1046/j.1540-8167.2003.02382.x. J Cardiovasc Electrophysiol. 2003. PMID: 12693506

8

[Genetics and cardiac arrhythmias].

Probst V, Kyndt F, Allouis M, Schott JJ, Le Marec H. Probst V, et al. Among authors: schott jj. Arch Mal Coeur Vaiss. 2003 Nov;96(11):1054-62. Arch Mal Coeur Vaiss. 2003. PMID: 14694781 Review. French.

9

A common antitussive drug, clobutinol, precipitates the long QT syndrome 2.

Bellocq C, Wilders R, Schott JJ, Louérat-Oriou B, Boisseau P, Le Marec H, Escande D, Baró I. Bellocq C, et al. Among authors: schott jj. Mol Pharmacol. 2004 Nov;66(5):1093-102. doi: 10.1124/mol.104.001065. Epub 2004 Jul 27. Mol Pharmacol. 2004. PMID: 15280442

10

Unusual clinical presentation in a family with catecholaminergic polymorphic ventricular tachycardia due to a G14876A ryanodine receptor gene mutation.

Allouis M, Probst V, Jaafar P, Schott JJ, Le Marec H. Allouis M, et al. Among authors: schott jj. Am J Cardiol. 2005 Mar 1;95(5):700-2. doi: 10.1016/j.amjcard.2004.10.057. Am J Cardiol. 2005. PMID: 15721128

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