Schott JJ - Search Results

1

TRPM4 non-selective cation channel variants in long QT syndrome.

Hof T, Liu H, Sallé L, Schott JJ, Ducreux C, Millat G, Chevalier P, Probst V, Guinamard R, Bouvagnet P. Hof T, et al. Among authors: schott jj. BMC Med Genet. 2017 Mar 18;18(1):31. doi: 10.1186/s12881-017-0397-4. BMC Med Genet. 2017. PMID: 28315637 Free PMC article.

2

Mapping of a gene for long QT syndrome to chromosome 4q25-27.

Schott JJ, Charpentier F, Peltier S, Foley P, Drouin E, Bouhour JB, Donnelly P, Vergnaud G, Bachner L, Moisan JP, et al. Schott JJ, et al. Am J Hum Genet. 1995 Nov;57(5):1114-22. Am J Hum Genet. 1995. PMID: 7485162 Free PMC article.

3

Cardiac conduction defects associate with mutations in SCN5A.

Schott JJ, Alshinawi C, Kyndt F, Probst V, Hoorntje TM, Hulsbeek M, Wilde AA, Escande D, Mannens MM, Le Marec H. Schott JJ, et al. Nat Genet. 1999 Sep;23(1):20-1. doi: 10.1038/12618. Nat Genet. 1999. PMID: 10471492 No abstract available.

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

Non-invasive testing of acquired long QT syndrome: evidence for multiple arrhythmogenic substrates.

Chevalier P, Rodriguez C, Bontemps L, Miquel M, Kirkorian G, Rousson R, Potet F, Schott JJ, Baró I, Touboul P. Chevalier P, et al. Among authors: schott jj. Cardiovasc Res. 2001 May;50(2):386-98. doi: 10.1016/s0008-6363(01)00263-2. Cardiovasc Res. 2001. PMID: 11334843

6

Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family.

Kyndt F, Probst V, Potet F, Demolombe S, Chevallier JC, Baro I, Moisan JP, Boisseau P, Schott JJ, Escande D, Le Marec H. Kyndt F, et al. Among authors: schott jj. Circulation. 2001 Dec 18;104(25):3081-6. doi: 10.1161/hc5001.100834. Circulation. 2001. PMID: 11748104

7

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.

8

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.

9

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

10

Cardiac retention of [11C]HED in genotyped long QT patients: a potential amplifier role for severity of the disease.

Mazzadi AN, André-Fouët X, Duisit J, Gebuhrer V, Costes N, Chevalier P, Rodriguez C, Schott JJ, Le Marec H, Guicheney P, Le Bars D, Janier M. Mazzadi AN, et al. Among authors: schott jj. Am J Physiol Heart Circ Physiol. 2003 Sep;285(3):H1286-93. doi: 10.1152/ajpheart.00276.2003. Epub 2003 May 29. Am J Physiol Heart Circ Physiol. 2003. PMID: 12775564 Free article. Clinical Trial.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

143 results

Search Page