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Catharina Whybra

Showing results (21-30 of 26) with videos related to

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International Journal of Cardiology|June 24, 2008
Onset and progression of the Anderson-Fabry disease related cardiomyopathyChristoph Kampmann, Ales Linhart, Frank Baehner, et al.
Journal of Neurology|March 3, 2006
Pattern of microstructural brain tissue alterations in Fabry disease: a diffusion-tensor imaging studyAndreas Fellgiebel, Martin Mazanek, Catharina Whybra, et al.
Journal of Perinatal Medicine|April 11, 2022
A single center experience in 90 cases with nonimmune hydrops fetalis: diagnostic categories ‒ mostly aneuploidy and still often idiopathicJulia Sturm, Heiko Milera, Stephanie Essmann, et al.
Health and Quality of Life Outcomes|September 21, 2012
Measuring patient experiences in Fabry disease: validation of the Fabry-specific Pediatric Health and Pain Questionnaire (FPHPQ)Uma Ramaswami, Donald E Stull, Rossella Parini, et al.
Pediatrics|September 5, 2006
Enzyme-replacement therapy with agalsidase alfa in children with Fabry diseaseMarkus Ries, Joe T R Clarke, Catharina Whybra, et al.
Human Mutation|March 19, 2005
Thirty-four novel mutations of the GLA gene in 121 patients with Fabry diseaseEllen Schäfer, Karin Baron, Urs Widmer, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
International Journal of Cardiology|June 24, 2008
Onset and progression of the Anderson-Fabry disease related cardiomyopathyChristoph Kampmann, Ales Linhart, Frank Baehner, et al.
Journal of Neurology|March 3, 2006
Pattern of microstructural brain tissue alterations in Fabry disease: a diffusion-tensor imaging studyAndreas Fellgiebel, Martin Mazanek, Catharina Whybra, et al.
Journal of Perinatal Medicine|April 11, 2022
A single center experience in 90 cases with nonimmune hydrops fetalis: diagnostic categories ‒ mostly aneuploidy and still often idiopathicJulia Sturm, Heiko Milera, Stephanie Essmann, et al.
Health and Quality of Life Outcomes|September 21, 2012
Measuring patient experiences in Fabry disease: validation of the Fabry-specific Pediatric Health and Pain Questionnaire (FPHPQ)Uma Ramaswami, Donald E Stull, Rossella Parini, et al.
Pediatrics|September 5, 2006
Enzyme-replacement therapy with agalsidase alfa in children with Fabry diseaseMarkus Ries, Joe T R Clarke, Catharina Whybra, et al.
Human Mutation|March 19, 2005
Thirty-four novel mutations of the GLA gene in 121 patients with Fabry diseaseEllen Schäfer, Karin Baron, Urs Widmer, et al.
Pageof 3