Kyndt F - Search Results

1

Ankyrin-B mutation causes type 4 long-QT cardiac arrhythmia and sudden cardiac death.

Mohler PJ, Schott JJ, Gramolini AO, Dilly KW, Guatimosim S, duBell WH, Song LS, Haurogné K, Kyndt F, Ali ME, Rogers TB, Lederer WJ, Escande D, Le Marec H, Bennett V. Mohler PJ, et al. Among authors: kyndt f. Nature. 2003 Feb 6;421(6923):634-9. doi: 10.1038/nature01335. Nature. 2003. PMID: 12571597

2

Mutations in a dominant-negative isoform correlate with phenotype in inherited cardiac arrhythmias.

Mohammad-Panah R, Demolombe S, Neyroud N, Guicheney P, Kyndt F, van den Hoff M, Baró I, Escande D. Mohammad-Panah R, et al. Among authors: kyndt f. Am J Hum Genet. 1999 Apr;64(4):1015-23. doi: 10.1086/302346. Am J Hum Genet. 1999. PMID: 10090886 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. Among authors: kyndt f. 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: kyndt f. 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

Dynamic analysis of the QT interval in long QT1 syndrome patients with a normal phenotype.

Lande G, Kyndt F, Baró I, Chabannes D, Boisseau P, Pony JC, Escande D, Le Marec H. Lande G, et al. Among authors: kyndt f. Eur Heart J. 2001 Mar;22(5):410-22. doi: 10.1053/euhj.2000.2292. Eur Heart J. 2001. PMID: 11207083 Clinical Trial.

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. 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: kyndt f. 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: kyndt f. 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

[Genetics and cardiac arrhythmias].

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

10

[Genetic aspects of cardiac conduction defects].

Probst V, Kyndt F, Allouis M, Schott JJ, Le Marec H. Probst V, et al. Among authors: kyndt f. Arch Mal Coeur Vaiss. 2003 Nov;96(11):1067-73. Arch Mal Coeur Vaiss. 2003. PMID: 14694782 Review. French.

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