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D P Germain

Showing results (1-10 of 49) with videos related to

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Pathologie-Biologie|July 21, 2004
[Gaucher disease: clinical, genetic and therapeutic aspects]D P Germain
Annales De Dermatologie Et De Venereologie|October 17, 2017
[Ehlers-Danlos syndromes]D-P Germain
La Revue De Medecine Interne|February 24, 2001
[Fabry disease. Clinical and genetic aspects. Therapeutic perspectives]D P Germain
Journal of Medical Genetics|July 28, 2001
Pseudoxanthoma elasticum: evidence for the existence of a pseudogene highly homologous to the ABCC6 geneD P Germain
Contributions to Nephrology|November 2, 2001
A new phenotype of Fabry disease with intermediate severity between the classical form and the cardiac variantD P Germain
Clinical Genetics|February 27, 2004
Gaucher's disease: a paradigm for interventional geneticsD P Germain
Clinical Genetics|September 5, 2001
Co-occurrence and contribution of Fabry disease and Klippel-Trénaunay-Weber syndrome to a patient with atypical skin lesionsD P Germain
La Revue De Medecine Interne|January 8, 2011
[Third French multidisciplinary meeting on Fabry disease]D P Germain
La Revue De Medecine Interne|February 2, 2008
[Prenatal diagnosis of Gaucher disease]D P Germain, K Benistan
International Journal of Clinical Pharmacology and Therapeutics|December 31, 2009
Current state of the management of LSDsD P Germain, M Aggio
Pageof 5

Showing results (1-10 of 49) with videos related to

Sort By:
Pageof 5
Pathologie-Biologie|July 21, 2004
[Gaucher disease: clinical, genetic and therapeutic aspects]D P Germain
Annales De Dermatologie Et De Venereologie|October 17, 2017
[Ehlers-Danlos syndromes]D-P Germain
La Revue De Medecine Interne|February 24, 2001
[Fabry disease. Clinical and genetic aspects. Therapeutic perspectives]D P Germain
Journal of Medical Genetics|July 28, 2001
Pseudoxanthoma elasticum: evidence for the existence of a pseudogene highly homologous to the ABCC6 geneD P Germain
Contributions to Nephrology|November 2, 2001
A new phenotype of Fabry disease with intermediate severity between the classical form and the cardiac variantD P Germain
Clinical Genetics|February 27, 2004
Gaucher's disease: a paradigm for interventional geneticsD P Germain
Clinical Genetics|September 5, 2001
Co-occurrence and contribution of Fabry disease and Klippel-Trénaunay-Weber syndrome to a patient with atypical skin lesionsD P Germain
La Revue De Medecine Interne|January 8, 2011
[Third French multidisciplinary meeting on Fabry disease]D P Germain
La Revue De Medecine Interne|February 2, 2008
[Prenatal diagnosis of Gaucher disease]D P Germain, K Benistan
International Journal of Clinical Pharmacology and Therapeutics|December 31, 2009
Current state of the management of LSDsD P Germain, M Aggio
Pageof 5