Leenhardt A - Search Results

1

Unusual clinical description of adult with Timothy syndrome, carrier of a new heterozygote mutation of CACNA1C.

Colson C, Mittre H, Busson A, Leenhardt A, Denjoy I, Fressard V, Troadec Y. Colson C, et al. Among authors: leenhardt a. Eur J Med Genet. 2019 Jul;62(7):103648. doi: 10.1016/j.ejmg.2019.04.005. Epub 2019 Apr 16. Eur J Med Genet. 2019. PMID: 30998997 Review.

2

[Value of signal-averaged electrocardiogram in ventricular arrhythmia without apparent heart disease].

Leclercq JF, Denjoy I, Maison-Blanche P, Cauchemez B, Leenhardt A, Coumel P, Slama R. Leclercq JF, et al. Among authors: leenhardt a. Arch Mal Coeur Vaiss. 1992 Jun;85(6):831-7. Arch Mal Coeur Vaiss. 1992. PMID: 1417401 French.

3

[Signal-averaged electrocardiography in right ventricular dysplasia].

Leclercq JF, Denjoy I, Maison-Blanche P, Cauchemez B, Leenhardt A, Slama R. Leclercq JF, et al. Among authors: leenhardt a. Arch Mal Coeur Vaiss. 1990 Apr;83(4):525-9. Arch Mal Coeur Vaiss. 1990. PMID: 2111673 French.

4

[Late potentials and arrhythmogenic right ventricular dysplasia].

Leclercq JF, Denjoy I, Maison-Blanche P, Cauchemez B, Leenhardt A, Coumel P, Slama R. Leclercq JF, et al. Among authors: leenhardt a. Ann Cardiol Angeiol (Paris). 1990 May;39(5):281-5. Ann Cardiol Angeiol (Paris). 1990. PMID: 2369065 French.

5

[Value of the exercise test in the study of arrhythmia].

Leenhardt A, Thomas O, Cauchemez B, Maison-Blanche P, Denjoy I, de Jode P, Kedra W, Coumel P. Leenhardt A, et al. Arch Mal Coeur Vaiss. 1995 Jan;88 Spec No 1:59-66. Arch Mal Coeur Vaiss. 1995. PMID: 7786146 Review. French.

6

Catecholaminergic polymorphic ventricular tachycardia in children. A 7-year follow-up of 21 patients.

Leenhardt A, Lucet V, Denjoy I, Grau F, Ngoc DD, Coumel P. Leenhardt A, et al. Circulation. 1995 Mar 1;91(5):1512-9. doi: 10.1161/01.cir.91.5.1512. Circulation. 1995. PMID: 7867192

7

[Dynamics of ventricular repolarisation].

Leenhardt A, Maison-Blanche P, Denjoy I, Neyroud N, Pellerin D, Catuli D, Thomas O, Coumel P. Leenhardt A, et al. Arch Mal Coeur Vaiss. 1995 Dec;88 Spec No 5:27-33. Arch Mal Coeur Vaiss. 1995. PMID: 8729297 French.

8

[QT interval and drugs. Recommendation for drug prescription for patients with long QT syndrome. Clinical Research Group of INSERM 4940 12: Diagnostic Clinic of Congenital Long QT Syndrome].

Le Heuzey JY, Davy JM, Weissenburger J, Guicheney P, Le Marec H, Chevalier P, Denjoy I, Leenhardt A, Charpentier F, Coumel P. Le Heuzey JY, et al. Among authors: leenhardt a. Arch Mal Coeur Vaiss. 1998 Jan;91(1):59-66. Arch Mal Coeur Vaiss. 1998. PMID: 9749265 Review. French.

9

Heterozygous mutation in the pore of potassium channel gene KvLQT1 causes an apparently normal phenotype in long QT syndrome.

Neyroud N, Denjoy I, Donger C, Gary F, Villain E, Leenhardt A, Benali K, Schwartz K, Coumel P, Guicheney P. Neyroud N, et al. Among authors: leenhardt a. Eur J Hum Genet. 1998 Mar-Apr;6(2):129-33. doi: 10.1038/sj.ejhg.5200165. Eur J Hum Genet. 1998. PMID: 9781056

10

[Mechanism of spontaneous occurrence of tachycardia].

Leenhardt A, Maison-Blanche P, Denjoy I, Cauchemez B, Joubert JP, Coumel P. Leenhardt A, et al. Arch Mal Coeur Vaiss. 1999 Apr;92 Spec No 1:17-22. Arch Mal Coeur Vaiss. 1999. PMID: 10326154 French.

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