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Acta Paediatrica (Oslo, Norway : 1992)
|
February 28, 2006
Clinical manifestations of Fabry disease in children: data from the Fabry Outcome Survey
Uma 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 Cases
Glenn K Geeting, Michael Beck, Michael A Bruno, et al.
Contact Dermatitis
|
February 9, 2010
Sensitization to dimethyl fumarate with multiple concurrent patch test reactions
Kaija 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 therapy
Christoph Kampmann, Christina Lampe, Catharina Whybra-Trümpler, et al.
Pediatric Dentistry
|
October 23, 2018
The Effects of Primary Canine Loss on Permanent Lower Dental Midline Stability
Robert 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 cells
Charlotte 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 Clinic
Abigail Nelson, Heather Stuckey, Bethany Snyder, et al.
Pediatric Nephrology (Berlin, Germany)
|
July 14, 2006
IgA nephropathy in two adolescent sisters heterozygous for Fabry disease
Catharina 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 Survey
Joseph Muenzer, Michael Beck, Roberto Giugliani, et al.
Page
of 24
Search research articles
Search
Showing results (131-140 of 233) with videos related to
Sort By:
Page
of 24
Acta Paediatrica (Oslo, Norway : 1992)
|
February 28, 2006
Clinical manifestations of Fabry disease in children: data from the Fabry Outcome Survey
Uma 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 Cases
Glenn K Geeting, Michael Beck, Michael A Bruno, et al.
Contact Dermatitis
|
February 9, 2010
Sensitization to dimethyl fumarate with multiple concurrent patch test reactions
Kaija 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 therapy
Christoph Kampmann, Christina Lampe, Catharina Whybra-Trümpler, et al.
Pediatric Dentistry
|
October 23, 2018
The Effects of Primary Canine Loss on Permanent Lower Dental Midline Stability
Robert 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 cells
Charlotte 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 Clinic
Abigail Nelson, Heather Stuckey, Bethany Snyder, et al.
Pediatric Nephrology (Berlin, Germany)
|
July 14, 2006
IgA nephropathy in two adolescent sisters heterozygous for Fabry disease
Catharina 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 Survey
Joseph Muenzer, Michael Beck, Roberto Giugliani, et al.
Page
of 24