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Journal of Inherited Metabolic Disease
|
June 22, 2012
Management of mucopolysaccharidosis type IH (Hurler's syndrome) presenting in infancy with severe dilated cardiomyopathy: a single institution's experience
Daniel H Wiseman, Jean Mercer, Karen Tylee, et al.
Journal of Inherited Metabolic Disease
|
January 22, 2011
Growth, final height and endocrine sequelae in a UK population of patients with Hurler syndrome (MPS1H)
Chris J Gardner, Nicola Robinson, Tim Meadows, et al.
The Journal of Heart Valve Disease
|
June 30, 2004
Thrombotic risk in patients with aortic bioprostheses
J J Edmond, S C Greaves, J K French, et al.
JIMD Reports
|
December 8, 2017
Haematopoietic Stem Cell Transplantation Arrests the Progression of Neurodegenerative Disease in Late-Onset Tay-Sachs Disease
Karolina M Stepien, Su Han Lum, J Edmond Wraith, et al.
The Journal of Biological Chemistry
|
December 5, 1986
Regulation of rat liver 3-hydroxy-3-methylglutaryl coenzyme A synthase and the chromosomal localization of the human gene
M Mehrabian, K A Callaway, C F Clarke, et al.
European Journal of Pediatrics
|
November 27, 2007
Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy
J Edmond Wraith, Maurizio Scarpa, Michael Beck, et al.
The American Journal of Cardiology
|
March 28, 2006
Frequency of recurrent ST-elevation myocardial infarction after fibrinolytic therapy in a different territory as a manifestation of multiple unstable coronary arterial plaques
John J Edmond, John K French, Ralph A H Stewart, et al.
The Journal of Biological Chemistry
|
November 1, 2014
Heparan sulfate inhibits hematopoietic stem and progenitor cell migration and engraftment in mucopolysaccharidosis I
H Angharad Watson, Rebecca J Holley, Kia J Langford-Smith, 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 I
Gregory M Pastores, Pamela Arn, Michael Beck, et al.
Pediatrics
|
January 2, 2009
Long-term efficacy and safety of laronidase in the treatment of mucopolysaccharidosis I
Lorne A Clarke, J Edmond Wraith, Michael Beck, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 108) with videos related to
Sort By:
Page
of 11
Journal of Inherited Metabolic Disease
|
June 22, 2012
Management of mucopolysaccharidosis type IH (Hurler's syndrome) presenting in infancy with severe dilated cardiomyopathy: a single institution's experience
Daniel H Wiseman, Jean Mercer, Karen Tylee, et al.
Journal of Inherited Metabolic Disease
|
January 22, 2011
Growth, final height and endocrine sequelae in a UK population of patients with Hurler syndrome (MPS1H)
Chris J Gardner, Nicola Robinson, Tim Meadows, et al.
The Journal of Heart Valve Disease
|
June 30, 2004
Thrombotic risk in patients with aortic bioprostheses
J J Edmond, S C Greaves, J K French, et al.
JIMD Reports
|
December 8, 2017
Haematopoietic Stem Cell Transplantation Arrests the Progression of Neurodegenerative Disease in Late-Onset Tay-Sachs Disease
Karolina M Stepien, Su Han Lum, J Edmond Wraith, et al.
The Journal of Biological Chemistry
|
December 5, 1986
Regulation of rat liver 3-hydroxy-3-methylglutaryl coenzyme A synthase and the chromosomal localization of the human gene
M Mehrabian, K A Callaway, C F Clarke, et al.
European Journal of Pediatrics
|
November 27, 2007
Mucopolysaccharidosis type II (Hunter syndrome): a clinical review and recommendations for treatment in the era of enzyme replacement therapy
J Edmond Wraith, Maurizio Scarpa, Michael Beck, et al.
The American Journal of Cardiology
|
March 28, 2006
Frequency of recurrent ST-elevation myocardial infarction after fibrinolytic therapy in a different territory as a manifestation of multiple unstable coronary arterial plaques
John J Edmond, John K French, Ralph A H Stewart, et al.
The Journal of Biological Chemistry
|
November 1, 2014
Heparan sulfate inhibits hematopoietic stem and progenitor cell migration and engraftment in mucopolysaccharidosis I
H Angharad Watson, Rebecca J Holley, Kia J Langford-Smith, 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 I
Gregory M Pastores, Pamela Arn, Michael Beck, et al.
Pediatrics
|
January 2, 2009
Long-term efficacy and safety of laronidase in the treatment of mucopolysaccharidosis I
Lorne A Clarke, J Edmond Wraith, Michael Beck, et al.
Page
of 11