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Michael Beck

Showing results (191-200 of 233) with videos related to

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American Journal of Medical Genetics. Part A|January 19, 2008
Molecular order in mucolipidosis II and III nomenclatureSara S Cathey, Mariko Kudo, Stephan Tiede, 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.
Journal of Inherited Metabolic Disease|February 7, 2013
Spinal involvement in mucopolysaccharidosis IVA (Morquio-Brailsford or Morquio A syndrome): presentation, diagnosis and managementGuirish A Solanki, Kenneth W Martin, Mary C Theroux, et al.
Pediatrics|January 2, 2009
Long-term efficacy and safety of laronidase in the treatment of mucopolysaccharidosis ILorne A Clarke, J Edmond Wraith, Michael Beck, et al.
Molecular Genetics and Metabolism|March 6, 2007
The MPS I registry: design, methodology, and early findings of a global disease registry for monitoring patients with Mucopolysaccharidosis Type IGregory M Pastores, Pamela Arn, Michael Beck, et al.
Orphanet Journal of Rare Diseases|June 7, 2015
Alpha-mannosidosis: correlation between phenotype, genotype and mutant MAN2B1 subcellular localisationLine Borgwardt, Hilde Monica Frostad Riise Stensland, Klaus Juul Olsen, 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.
Kidney International|April 21, 2005
Anemia is a new complication in Fabry disease: data from the Fabry Outcome SurveyJulia Kleinert, François Dehout, Andreas Schwarting, et al.
American Journal of Hypertension|August 1, 2006
Prevalence of uncontrolled hypertension in patients with Fabry diseaseJulia Kleinert, François Dehout, Andreas Schwarting, et al.
The Prostate|November 7, 2017
<sup>99m</sup> Tc-MIP-1404-SPECT/CT for the detection of PSMA-positive lesions in 225 patients with biochemical recurrence of prostate cancerChristian Schmidkonz, Claudia Hollweg, Michael Beck, et al.
Pageof 24

Showing results (191-200 of 233) with videos related to

Sort By:
Pageof 24
American Journal of Medical Genetics. Part A|January 19, 2008
Molecular order in mucolipidosis II and III nomenclatureSara S Cathey, Mariko Kudo, Stephan Tiede, 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.
Journal of Inherited Metabolic Disease|February 7, 2013
Spinal involvement in mucopolysaccharidosis IVA (Morquio-Brailsford or Morquio A syndrome): presentation, diagnosis and managementGuirish A Solanki, Kenneth W Martin, Mary C Theroux, et al.
Pediatrics|January 2, 2009
Long-term efficacy and safety of laronidase in the treatment of mucopolysaccharidosis ILorne A Clarke, J Edmond Wraith, Michael Beck, et al.
Molecular Genetics and Metabolism|March 6, 2007
The MPS I registry: design, methodology, and early findings of a global disease registry for monitoring patients with Mucopolysaccharidosis Type IGregory M Pastores, Pamela Arn, Michael Beck, et al.
Orphanet Journal of Rare Diseases|June 7, 2015
Alpha-mannosidosis: correlation between phenotype, genotype and mutant MAN2B1 subcellular localisationLine Borgwardt, Hilde Monica Frostad Riise Stensland, Klaus Juul Olsen, 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.
Kidney International|April 21, 2005
Anemia is a new complication in Fabry disease: data from the Fabry Outcome SurveyJulia Kleinert, François Dehout, Andreas Schwarting, et al.
American Journal of Hypertension|August 1, 2006
Prevalence of uncontrolled hypertension in patients with Fabry diseaseJulia Kleinert, François Dehout, Andreas Schwarting, et al.
The Prostate|November 7, 2017
<sup>99m</sup> Tc-MIP-1404-SPECT/CT for the detection of PSMA-positive lesions in 225 patients with biochemical recurrence of prostate cancerChristian Schmidkonz, Claudia Hollweg, Michael Beck, et al.
Pageof 24