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P Germain

Showing results (211-220 of 332) with videos related to

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Annales De Cardiologie Et D'Angeiologie|July 1, 1986
[Diagnostic elements of a right papyraceous ventricle. The value of nuclear magnetic resonance]M Hanssen, J M Mossard, P Germain, et al.
Molecular Genetics and Metabolism Reports|January 18, 2024
Use of T1 mapping in cardiac MRI for the follow-up of Fabry disease in a pediatric populationOscar Werner, Lydia Ichay, Nabila Djouadi, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|October 1, 1989
[Value of cine magnetic resonance imaging in the diagnosis and quantification of valvular regurgitation. Comparison with angiography and Doppler echocardiography]P Germain, J Baruthio, G Roul, et al.
Analytical and Bioanalytical Chemistry|June 17, 2005
Fast fingerprinting by MALDI-TOF mass spectrometry of urinary sediment glycosphingolipids in Fabry diseaseDavid Touboul, Sandrine Roy, Dominique P Germain, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 23, 2008
Successful reinstitution of agalsidase beta therapy in Fabry disease patients with previous IgE-antibody or skin-test reactivity to the recombinant enzymeDavid Bodensteiner, C Ronald Scott, Katherine B Sims, et al.
Pediatric Radiology|January 1, 1992
Contribution of MRI in supracardiac total anomalous pulmonary venous drainageB Kastler, A Livolsi, P Germain, et al.
Revue Des Maladies Respiratoires|October 24, 2008
[Niemann-Pick disease type B identified following an episode of bronchopneumonia]A Hervé, S Marchand-Adam, A Fabre, et al.
Journal of Neurology|November 19, 2011
The pulvinar sign in Fabry patients: the first report in female patientsAlessandro P Burlina, Juan Politei, Sarah Cinque, et al.
La Revue De Medecine Interne|July 28, 2004
[Pulmonary plasmacytoma: about two new cases and review of the literature]G Etienne, M Grenouillet, C Ghiringhelli, et al.
Molecular Genetics and Metabolism|August 15, 2008
Enzyme replacement therapy in Fabry disease: comparison of agalsidase alfa and agalsidase betaAtul Mehta, Michael Beck, Christoph Kampmann, et al.
Pageof 34

Showing results (211-220 of 332) with videos related to

Sort By:
Pageof 34
Annales De Cardiologie Et D'Angeiologie|July 1, 1986
[Diagnostic elements of a right papyraceous ventricle. The value of nuclear magnetic resonance]M Hanssen, J M Mossard, P Germain, et al.
Molecular Genetics and Metabolism Reports|January 18, 2024
Use of T1 mapping in cardiac MRI for the follow-up of Fabry disease in a pediatric populationOscar Werner, Lydia Ichay, Nabila Djouadi, et al.
Archives Des Maladies Du Coeur Et Des Vaisseaux|October 1, 1989
[Value of cine magnetic resonance imaging in the diagnosis and quantification of valvular regurgitation. Comparison with angiography and Doppler echocardiography]P Germain, J Baruthio, G Roul, et al.
Analytical and Bioanalytical Chemistry|June 17, 2005
Fast fingerprinting by MALDI-TOF mass spectrometry of urinary sediment glycosphingolipids in Fabry diseaseDavid Touboul, Sandrine Roy, Dominique P Germain, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 23, 2008
Successful reinstitution of agalsidase beta therapy in Fabry disease patients with previous IgE-antibody or skin-test reactivity to the recombinant enzymeDavid Bodensteiner, C Ronald Scott, Katherine B Sims, et al.
Pediatric Radiology|January 1, 1992
Contribution of MRI in supracardiac total anomalous pulmonary venous drainageB Kastler, A Livolsi, P Germain, et al.
Revue Des Maladies Respiratoires|October 24, 2008
[Niemann-Pick disease type B identified following an episode of bronchopneumonia]A Hervé, S Marchand-Adam, A Fabre, et al.
Journal of Neurology|November 19, 2011
The pulvinar sign in Fabry patients: the first report in female patientsAlessandro P Burlina, Juan Politei, Sarah Cinque, et al.
La Revue De Medecine Interne|July 28, 2004
[Pulmonary plasmacytoma: about two new cases and review of the literature]G Etienne, M Grenouillet, C Ghiringhelli, et al.
Molecular Genetics and Metabolism|August 15, 2008
Enzyme replacement therapy in Fabry disease: comparison of agalsidase alfa and agalsidase betaAtul Mehta, Michael Beck, Christoph Kampmann, et al.
Pageof 34