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Neuropeptides|June 1, 1994
Effect of the slow-release formulation of somatuline (BIM 23014) on estrogen-induced hyperprolactinemia and lactotroph hyperplasia in the female ratN Schussler, R Farnoud, C Rauch, et al.
European Journal of Endocrinology|February 1, 1995
Stimulatory effect of gonadotropin-releasing hormone (GnRH) on in vitro prolactin secretion and presence of GnRH specific receptors in a subset of human prolactinomasA M Brandi, G Barrande, N Lahlou, et al.
European Journal of Human Genetics : EJHG|May 31, 2007
Confirmation of associations between ion channel gene SNPs and QTc interval duration in healthy subjectsL Gouas, V Nicaud, S Chaouch, et al.
Journal of Molecular and Cellular Cardiology|September 1, 1996
Exclusion of KCNE1 (IsK) as a candidate gene for Jervell and Lange-Nielsen syndromeF Tesson, C Donger, I Denjoy, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|June 28, 2002
[Homozygotous mutation of the SCN5A gene responsible for congenital long QT syndrome with 2/1 atrioventricular block]J M Lupoglazoff, I Denjoy, T Cheav, et al.
Circulation Research|July 21, 2001
Homozygous SCN5A mutation in long-QT syndrome with functional two-to-one atrioventricular blockJ M Lupoglazoff, T Cheav, G Baroudi, et al.
Circulation|December 31, 1997
KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndromeC Donger, I Denjoy, M Berthet, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|June 15, 1999
[Congenital long QT syndrome. The value of genetics in prognostic evaluation]I Denjoy, J M Lupoglazoff, C Donger, et al.
British Journal of Anaesthesia|January 13, 2017
Reduced mortality by meeting guideline criteria before using recombinant activated factor VII in severe trauma patients with massive bleedingJ-F Payen, M Berthet, C Genty, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|July 4, 2001
[T wave abnormalities on Holter monitoring of congenital long QT syndrome: phenotypic marker of a mutation of LQT2 (HERG)]J M Lupoglazoff, I Denjoy, M Berthet, et al.
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