Dexrazoxane protects the heart from acute doxorubicin‐induced QT prolongation: a key role for IKs von Ducroq, J, Moha ou Maati, H, Guilbot, S, Dilly, S, Laemmel, E, Pons‐Himbert, C, Faivre, JF, Bois, P, Stücker, O, Le Grand, M

Volltext

Dexrazoxane protects the heart from acute doxorubicin‐induced QT prolongation: a key role for I Ks von Ducroq, J, Moha ou Maati, H, Guilbot, S, Dilly, S, Laemmel, E, Pons‐Himbert, C, Faivre, JF, Bois, P, Stücker, O, Le Grand, M

Volltext

Les pieux maritimes du pont Vasco da Gama von Wastiaux, M., Ducroq, J., Corbetta, F.

Volltext

Dexrazoxane protects the heart from acute doxorubicin-induced QT prolongation: a key role for IKs : QT Safety von DUCROQ, J, MOHA OU MAATI, H, GUILBOT, S, DILLY, S, LAEMMEL, E, PONS-HIMBERT, C, FAIVRE, J. F, BOIS, P, STÜCKER, O, LE GRAND, M

Volltext

Electrophysiological effects of azimilide in an in vitro model of simulated-ischemia and reperfusion in guinea-pig ventricular myocardium von Ducroq, Joffrey, Rouet, René, Puddu, Paolo Emilio, Sallé, Laurent, Tabourel, Clément, Ducouret, Pierre, Gérard, Jean-Louis

Volltext

Spécificités des interventions dans le cadre de catastrophes naturelles von Guillaumont, C, Maltais, Danielle

Volltext bestellen

Pont Vasco de Gama : les fondations maritimes von WASTIAUX, M, DUCROQ, J, BAGUELIN, F

Volltext

Sensitivity and Specificity of the In Vitro Guinea Pig Papillary Muscle Action Potential Duration for the Assessment of Drug-Induced Torsades De Pointes Liability in Humans von Ducroq, Joffrey

Volltext

Leber congenital amaurosis: Comprehensive survey of the genetic heterogeneity, refinement of the clinical definition, and genotype–phenotype correlations as a strategy for molecula... von Hanein, Sylvain, Perrault, Isabelle, Gerber, Sylvie, Tanguy, Gaëlle, Barbet, Fabienne, Ducroq, Dominique, Calvas, Patrick, Dollfus, Hélène, Hamel, Christian, Lopponen, Tuija, Munier, Francis, Santos, Louisa, Shalev, Stavit, Zafeiriou, Dimitrios, Dufier, Jean‐Louis, Munnich, Arnold, Rozet, Jean‐Michel, Kaplan, Josseline

Volltext

The effect of serum matrix and gender on cortisol measurement by commonly used immunoassays von Dodd, AJ, Ducroq, DH, Neale, SM, Wise, MP, Mitchem, KL, Armston, A, Barth, JH, El-Farhan, N, Rees, DA, Evans, C

Volltext

Retinal Dehydrogenase 12 ( RDH12) Mutations in Leber Congenital Amaurosis von Perrault, Isabelle, Hanein, Sylvain, Gerber, Sylvie, Barbet, Fabienne, Ducroq, Dominique, Dollfus, Helene, Hamel, Christian, Dufier, Jean-Louis, Munnich, Arnold, Kaplan, Josseline, Rozet, Jean-Michel

Volltext

Different Functional Outcome of RetGC1 and RPE65 Gene Mutations in Leber Congenital Amaurosis von Perrault, Isabelle, Rozet, Jean-Michel, Ghazi, Imad, Leowski, Corinne, Bonnemaison, Michèle, Gerber, Sylvie, Ducroq, Dominique, Cabot, Annick, Souied, Eric, Dufier, Jean-Louis, Munnich, Arnold, Kaplan, Josseline

Volltext

Complete exon-intron structure of the RPGR-interacting protein (RPGRIP1) gene allows the identification of mutations underlying Leber congenital amaurosis von Gerber, S, Perrault, I, Hanein, S, Barbet, F, Ducroq, D, Ghazi, I, Martin-Coignard, D, Leowski, C, Homfray, T, Dufier, J L, Munnich, A, Kaplan, J, Rozet, J M

Volltext

A third locus for dominant optic atrophy on chromosome 22q von Barbet, F, Hakiki, S, Orssaud, C, Gerber, S, Perrault, I, Hanein, S, Ducroq, D, Dufier, J-L, Munnich, A, Kaplan, J, Rozet, J-M

Volltext

Les effets de l'exposition chronique aux phtalates sur les comportements sexuel et cognitif chez la souris mâle adulte von Ducroq, Suzanne

Volltext bestellen

Spectrum of retGC1 mutations in Leber's congenital amaurosis von Perrault, I, Rozet, J M, Gerber, S, Ghazi, I, Ducroq, D, Souied, E, Leowski, C, Bonnemaison, M, Dufier, J L, Munnich, A, Kaplan, J

Volltext

A Gene for X-Linked Idiopathic Congenital Nystagmus (NYS1) Maps to Chromosome Xp11.4-p11.3 von Cabot, Annick, Rozet, Jean-Michel, Gerber, Sylvie, Perrault, Isabelle, Ducroq, Dominique, Smahi, Asmae, Souied, Eric, Munnich, Arnold, Kaplan, Josseline

Volltext

Human cytomegalovirus-infected cells have unstable assembly of major histocompatibility complex class I complexes and are resistant to lysis by cytotoxic T lymphocytes von WARREN, A. P, DUCROQ, D. H, LEHNER, P. J, BORYSIEWICZ, L. K

Volltext

Mutations of the retinal specific ATP binding transporter gene (ABCR) in a single family segregating both autosomal recessive retinitis pigmentosa RP19 and Stargardt disease: evide... von Rozet, Jean-Michet, Gerber, Sylvie, Ghazi, Imad, Perrault, Isabelle, Ducroq, Dominique, Souied, Eric, Cabot, Annick, Dufier, Jean-Louis, Munnich, Arnold, Kaplan, Josseline

Volltext

Leber Congenital Amaurosis von Perrault, Isabelle, Rozet, Jean-Michel, Gerber, Sylvie, Ghazi, Imad, Leowski, Corinne, Ducroq, Dominique, Souied, Eric, Dufier, Jean-Louis, Munnich, Arnold, Kaplan, Josseline

Volltext