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P Germain

Showing results (41-50 of 332) with videos related to

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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
Biochemical and Biophysical Research Communications|April 20, 1999
Fabry disease: identification of novel alpha-galactosidase A mutations and molecular carrier detection by use of fluorescent chemical cleavage of mismatchesD P Germain, L Poenaru
Clinical Genetics|January 10, 2003
Fabry disease: a functional and anatomical study of cardiac manifestations in 20 hemizygous male patientsM Senechal, D P Germain
La Revue De Medecine Interne|April 29, 2006
Phenotype variations in Gaucher diseaseP Mistry, D P Germain
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 27, 2014
[Genetic aspects of mucopolysaccharidoses]D Lacombe, D P Germain
Handbook of Clinical Neurology|December 25, 2013
Neurologic manifestations of inherited disorders of connective tissueStéphanie Debette, Dominique P Germain
Frontiers in Genetics|April 29, 2024
Pegunigalsidase alfa: a novel, pegylated recombinant alpha-galactosidase enzyme for the treatment of Fabry diseaseDominique P Germain, Ales Linhart
La Revue De Medecine Interne|January 30, 2008
[Therapeutic objectives in Gaucher disease]P Mistry, D P Germain
Human Mutation|January 4, 2001
Identification of novel polymorphisms in the pM5 and MRP1 (ABCC1) genes at locus 16p13.1 and exclusion of both genes as responsible for pseudoxanthoma elasticumJ Perdu, D P Germain
Pageof 34

Showing results (41-50 of 332) with videos related to

Sort By:
Pageof 34
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
Biochemical and Biophysical Research Communications|April 20, 1999
Fabry disease: identification of novel alpha-galactosidase A mutations and molecular carrier detection by use of fluorescent chemical cleavage of mismatchesD P Germain, L Poenaru
Clinical Genetics|January 10, 2003
Fabry disease: a functional and anatomical study of cardiac manifestations in 20 hemizygous male patientsM Senechal, D P Germain
La Revue De Medecine Interne|April 29, 2006
Phenotype variations in Gaucher diseaseP Mistry, D P Germain
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|July 27, 2014
[Genetic aspects of mucopolysaccharidoses]D Lacombe, D P Germain
Handbook of Clinical Neurology|December 25, 2013
Neurologic manifestations of inherited disorders of connective tissueStéphanie Debette, Dominique P Germain
Frontiers in Genetics|April 29, 2024
Pegunigalsidase alfa: a novel, pegylated recombinant alpha-galactosidase enzyme for the treatment of Fabry diseaseDominique P Germain, Ales Linhart
La Revue De Medecine Interne|January 30, 2008
[Therapeutic objectives in Gaucher disease]P Mistry, D P Germain
Human Mutation|January 4, 2001
Identification of novel polymorphisms in the pM5 and MRP1 (ABCC1) genes at locus 16p13.1 and exclusion of both genes as responsible for pseudoxanthoma elasticumJ Perdu, D P Germain
Pageof 34