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D P Germain

Showing results (41-50 of 49) with videos related to

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AJNR. American Journal of Neuroradiology|January 28, 2017
Basilar Artery Changes in Fabry DiseaseR Manara, R Y Carlier, S Righetto, et al.
Journal of Inherited Metabolic Disease|July 11, 2007
Natural history of the respiratory involvement in Anderson-Fabry diseaseS Magage, J-C Lubanda, Z Susa, et al.
QJM : Monthly Journal of the Association of Physicians|July 28, 2010
Fabry disease: a review of current management strategiesA Mehta, M Beck, F Eyskens, et al.
The New England Journal of Medicine|July 7, 2001
Safety and efficacy of recombinant human alpha-galactosidase A replacement therapy in Fabry's diseaseC M Eng, N Guffon, W R Wilcox, et al.
Prenatal Diagnosis|March 4, 2000
Prenatal diagnosis of pyloric atresia-junctional epidermolysis bullosa syndrome in a fetus not known to be at riskC Lépinard, P Descamps, G Meneguzzi, et al.
Clinical Genetics|May 15, 2015
X-chromosome inactivation in female patients with Fabry diseaseL Echevarria, K Benistan, A Toussaint, et al.
Molecular Genetics and Metabolism|March 12, 2013
A Phase 2 study of migalastat hydrochloride in females with Fabry disease: selection of population, safety and pharmacodynamic effectsR Giugliani, S Waldek, D P Germain, et al.
Journal of Inherited Metabolic Disease|March 10, 2007
Fabry disease: baseline medical characteristics of a cohort of 1765 males and females in the Fabry RegistryC M Eng, J Fletcher, W R Wilcox, et al.
La Revue De Medecine Interne|January 8, 2011
[Enzyme replacement therapy of lysosomal storage diseases]D P Germain, C Boucly, R Y Carlier, et al.
Pageof 5

Showing results (41-50 of 49) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 49 results.
AJNR. American Journal of Neuroradiology|January 28, 2017
Basilar Artery Changes in Fabry DiseaseR Manara, R Y Carlier, S Righetto, et al.
Journal of Inherited Metabolic Disease|July 11, 2007
Natural history of the respiratory involvement in Anderson-Fabry diseaseS Magage, J-C Lubanda, Z Susa, et al.
QJM : Monthly Journal of the Association of Physicians|July 28, 2010
Fabry disease: a review of current management strategiesA Mehta, M Beck, F Eyskens, et al.
The New England Journal of Medicine|July 7, 2001
Safety and efficacy of recombinant human alpha-galactosidase A replacement therapy in Fabry's diseaseC M Eng, N Guffon, W R Wilcox, et al.
Prenatal Diagnosis|March 4, 2000
Prenatal diagnosis of pyloric atresia-junctional epidermolysis bullosa syndrome in a fetus not known to be at riskC Lépinard, P Descamps, G Meneguzzi, et al.
Clinical Genetics|May 15, 2015
X-chromosome inactivation in female patients with Fabry diseaseL Echevarria, K Benistan, A Toussaint, et al.
Molecular Genetics and Metabolism|March 12, 2013
A Phase 2 study of migalastat hydrochloride in females with Fabry disease: selection of population, safety and pharmacodynamic effectsR Giugliani, S Waldek, D P Germain, et al.
Journal of Inherited Metabolic Disease|March 10, 2007
Fabry disease: baseline medical characteristics of a cohort of 1765 males and females in the Fabry RegistryC M Eng, J Fletcher, W R Wilcox, et al.
La Revue De Medecine Interne|January 8, 2011
[Enzyme replacement therapy of lysosomal storage diseases]D P Germain, C Boucly, R Y Carlier, et al.
Pageof 5