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Michael Beck

Showing results (131-140 of 233) with videos related to

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Acta Paediatrica (Oslo, Norway : 1992)|February 28, 2006
Clinical manifestations of Fabry disease in children: data from the Fabry Outcome SurveyUma Ramaswami, Catharina Whybra, Rosella Parini, et al.
AJR. American Journal of Roentgenology|May 5, 2016
Mandatory Assignment of Modified Wells Score Before CT Angiography for Pulmonary Embolism Fails to Improve Utilization or Percentage of Positive CasesGlenn K Geeting, Michael Beck, Michael A Bruno, et al.
Contact Dermatitis|February 9, 2010
Sensitization to dimethyl fumarate with multiple concurrent patch test reactionsKaija Lammintausta, Erik Zimerson, Sandra Winhoven, et al.
Journal of Inherited Metabolic Disease|September 25, 2013
Mucopolysaccharidosis VI: cardiac involvement and the impact of enzyme replacement therapyChristoph Kampmann, Christina Lampe, Catharina Whybra-Trümpler, et al.
Pediatric Dentistry|October 23, 2018
The Effects of Primary Canine Loss on Permanent Lower Dental Midline StabilityRobert T Christensen, Henry W Fields, John R Christensen, et al.
JIMD Reports|April 13, 2013
Development of a Scoring System to Evaluate the Severity of Craniocervical Spinal Cord Compression in Patients with Mucopolysaccharidosis IVA (Morquio A Syndrome)Christian Möllmann, Christian G Lampe, Wibke Müller-Forell, et al.
International Journal of Radiation Biology|May 23, 2013
Differential response to acute low dose radiation in primary and immortalized endothelial cellsCharlotte Rombouts, An Aerts, Michael Beck, et al.
Clinical Pediatrics|February 2, 2023
Provider Perspectives of Transitions of Care at a Tertiary Care Children's Hospital With a Hospitalist-Run Discharge ClinicAbigail Nelson, Heather Stuckey, Bethany Snyder, et al.
Pediatric Nephrology (Berlin, Germany)|July 14, 2006
IgA nephropathy in two adolescent sisters heterozygous for Fabry diseaseCatharina Whybra, Andreas Schwarting, Jörg Kriegsmann, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 15, 2011
Idursulfase treatment of Hunter syndrome in children younger than 6 years: results from the Hunter Outcome SurveyJoseph Muenzer, Michael Beck, Roberto Giugliani, et al.
Pageof 24

Showing results (131-140 of 233) with videos related to

Sort By:
Pageof 24
Acta Paediatrica (Oslo, Norway : 1992)|February 28, 2006
Clinical manifestations of Fabry disease in children: data from the Fabry Outcome SurveyUma Ramaswami, Catharina Whybra, Rosella Parini, et al.
AJR. American Journal of Roentgenology|May 5, 2016
Mandatory Assignment of Modified Wells Score Before CT Angiography for Pulmonary Embolism Fails to Improve Utilization or Percentage of Positive CasesGlenn K Geeting, Michael Beck, Michael A Bruno, et al.
Contact Dermatitis|February 9, 2010
Sensitization to dimethyl fumarate with multiple concurrent patch test reactionsKaija Lammintausta, Erik Zimerson, Sandra Winhoven, et al.
Journal of Inherited Metabolic Disease|September 25, 2013
Mucopolysaccharidosis VI: cardiac involvement and the impact of enzyme replacement therapyChristoph Kampmann, Christina Lampe, Catharina Whybra-Trümpler, et al.
Pediatric Dentistry|October 23, 2018
The Effects of Primary Canine Loss on Permanent Lower Dental Midline StabilityRobert T Christensen, Henry W Fields, John R Christensen, et al.
JIMD Reports|April 13, 2013
Development of a Scoring System to Evaluate the Severity of Craniocervical Spinal Cord Compression in Patients with Mucopolysaccharidosis IVA (Morquio A Syndrome)Christian Möllmann, Christian G Lampe, Wibke Müller-Forell, et al.
International Journal of Radiation Biology|May 23, 2013
Differential response to acute low dose radiation in primary and immortalized endothelial cellsCharlotte Rombouts, An Aerts, Michael Beck, et al.
Clinical Pediatrics|February 2, 2023
Provider Perspectives of Transitions of Care at a Tertiary Care Children's Hospital With a Hospitalist-Run Discharge ClinicAbigail Nelson, Heather Stuckey, Bethany Snyder, et al.
Pediatric Nephrology (Berlin, Germany)|July 14, 2006
IgA nephropathy in two adolescent sisters heterozygous for Fabry diseaseCatharina Whybra, Andreas Schwarting, Jörg Kriegsmann, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 15, 2011
Idursulfase treatment of Hunter syndrome in children younger than 6 years: results from the Hunter Outcome SurveyJoseph Muenzer, Michael Beck, Roberto Giugliani, et al.
Pageof 24