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R Jaussaud

Showing results (41-50 of 51) with videos related to

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International Journal of Clinical Practice|August 31, 2006
Hyperhidrosis: a new and often early symptom in Fabry disease. International experience and data from the Fabry Outcome SurveyO Lidove, U Ramaswami, R Jaussaud, et al.
Orphanet Journal of Rare Diseases|June 24, 2016
Does the route of immunoglobin replacement therapy impact quality of life and satisfaction in patients with primary immunodeficiency? Insights from the French cohort "Visages"B Bienvenu, G Cozon, C Hoarau, et al.
Revue Neurologique|October 3, 2008
[Nocardia brain abscess: features, therapeutic strategies and outcome]D Marnet, L Brasme, P Peruzzi, et al.
La Revue De Medecine Interne|September 11, 2019
[Diagnostic journey of type 1 Gaucher Disease patients: A survey including internists and hematologists]S Deriaz, C Serratrice, O Lidove, et al.
British Journal of Clinical Pharmacology|May 21, 2004
Population pharmacokinetics of pyrimethamine and sulfadoxine in children with congenital toxoplasmosisT Trenque, N Simon, I Villena, et al.
International Journal of Clinical Practice|January 12, 2013
Multidimensional analysis of clinical symptoms in patients with Fabry's diseaseP Kaminsky, E Noel, R Jaussaud, et al.
Journal of Inherited Metabolic Disease|June 10, 2010
The neurological manifestations of Gaucher disease type 1: the French Observatoire on Gaucher disease (FROG)P Chérin, C Rose, C de Roux-Serratrice, et al.
The British Journal of Dermatology|June 19, 2007
Fabry disease and the skin: data from FOS, the Fabry outcome surveyC H Orteu, T Jansen, O Lidove, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|August 5, 2010
Vertebral fractures in Gaucher disease type I: data from the French "Observatoire" on Gaucher disease (FROG)R-M Javier, E Hachulla, C Rose, et al.
La Revue De Medecine Interne|May 25, 2010
[Result of the survey on orphan disorders by the internal medicine--lysosomal diseases group]P Chérin, D Adoué, E Hachulla, et al.
Pageof 6

Showing results (41-50 of 51) with videos related to

Sort By:
Pageof 6
International Journal of Clinical Practice|August 31, 2006
Hyperhidrosis: a new and often early symptom in Fabry disease. International experience and data from the Fabry Outcome SurveyO Lidove, U Ramaswami, R Jaussaud, et al.
Orphanet Journal of Rare Diseases|June 24, 2016
Does the route of immunoglobin replacement therapy impact quality of life and satisfaction in patients with primary immunodeficiency? Insights from the French cohort "Visages"B Bienvenu, G Cozon, C Hoarau, et al.
Revue Neurologique|October 3, 2008
[Nocardia brain abscess: features, therapeutic strategies and outcome]D Marnet, L Brasme, P Peruzzi, et al.
La Revue De Medecine Interne|September 11, 2019
[Diagnostic journey of type 1 Gaucher Disease patients: A survey including internists and hematologists]S Deriaz, C Serratrice, O Lidove, et al.
British Journal of Clinical Pharmacology|May 21, 2004
Population pharmacokinetics of pyrimethamine and sulfadoxine in children with congenital toxoplasmosisT Trenque, N Simon, I Villena, et al.
International Journal of Clinical Practice|January 12, 2013
Multidimensional analysis of clinical symptoms in patients with Fabry's diseaseP Kaminsky, E Noel, R Jaussaud, et al.
Journal of Inherited Metabolic Disease|June 10, 2010
The neurological manifestations of Gaucher disease type 1: the French Observatoire on Gaucher disease (FROG)P Chérin, C Rose, C de Roux-Serratrice, et al.
The British Journal of Dermatology|June 19, 2007
Fabry disease and the skin: data from FOS, the Fabry outcome surveyC H Orteu, T Jansen, O Lidove, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|August 5, 2010
Vertebral fractures in Gaucher disease type I: data from the French "Observatoire" on Gaucher disease (FROG)R-M Javier, E Hachulla, C Rose, et al.
La Revue De Medecine Interne|May 25, 2010
[Result of the survey on orphan disorders by the internal medicine--lysosomal diseases group]P Chérin, D Adoué, E Hachulla, et al.
Pageof 6