Search research articles
Contact Us
Filters
Showing results (101-110 of 108) with videos related to
Page
of 11
Sort By:
You have reached the last page of results.
This site can display upto 108 results.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
June 11, 2013
Myeloid/Microglial driven autologous hematopoietic stem cell gene therapy corrects a neuronopathic lysosomal disease
Ana Sergijenko, Alexander Langford-Smith, Ai Y Liao, et al.
Hepatology (Baltimore, Md.)
|
January 26, 2013
Clinical effect and safety profile of recombinant human lysosomal acid lipase in patients with cholesteryl ester storage disease
Manisha Balwani, Catherine Breen, Gregory M Enns, et al.
European Heart Journal
|
May 15, 2007
Variations in the use of emergency PCI for the treatment of re-infarction following intravenous fibrinolytic therapy: impact on outcomes in HERO-2
J J Edmond, J K French, P E G Aylward, et al.
The Journal of Pediatrics
|
May 2, 2006
Enzyme replacement therapy for mucopolysaccharidosis VI: a phase 3, randomized, double-blind, placebo-controlled, multinational study of recombinant human N-acetylgalactosamine 4-sulfatase (recombinant human arylsulfatase B or rhASB) and follow-on, open-label extension study
Paul Harmatz, Roberto Giugliani, Ida Schwartz, et al.
Molecular Genetics and Metabolism
|
May 27, 2008
Long-term follow-up of endurance and safety outcomes during enzyme replacement therapy for mucopolysaccharidosis VI: Final results of three clinical studies of recombinant human N-acetylgalactosamine 4-sulfatase
Paul Harmatz, Roberto Giugliani, Ida Vanessa D Schwartz, et al.
Journal of Pediatric Rehabilitation Medicine
|
July 17, 2010
Enzyme replacement therapy for mucopolysaccharidosis VI: Growth and pubertal development in patients treated with recombinant human N-acetylgalactosamine 4-sulfatase
Celeste Decker, Zi-Fan Yu, Roberto Giugliani, et al.
Orphanet Journal of Rare Diseases
|
April 25, 2012
Capturing phenotypic heterogeneity in MPS I: results of an international consensus procedure
Minke H de Ru, Quirine Ga Teunissen, Johanna H van der Lee, et al.
Journal of Inherited Metabolic Disease
|
February 9, 2010
Enzyme replacement therapy for mucopolysaccharidosis VI: evaluation of long-term pulmonary function in patients treated with recombinant human N-acetylgalactosamine 4-sulfatase
Paul Harmatz, Zi-Fan Yu, Roberto Giugliani, et al.
Page
of 11
Search research articles
Search
Showing results (101-110 of 108) with videos related to
Sort By:
Page
of 11
You have reached the last page of results.
This site can display upto 108 results.
Molecular Therapy : the Journal of the American Society of Gene Therapy
|
June 11, 2013
Myeloid/Microglial driven autologous hematopoietic stem cell gene therapy corrects a neuronopathic lysosomal disease
Ana Sergijenko, Alexander Langford-Smith, Ai Y Liao, et al.
Hepatology (Baltimore, Md.)
|
January 26, 2013
Clinical effect and safety profile of recombinant human lysosomal acid lipase in patients with cholesteryl ester storage disease
Manisha Balwani, Catherine Breen, Gregory M Enns, et al.
European Heart Journal
|
May 15, 2007
Variations in the use of emergency PCI for the treatment of re-infarction following intravenous fibrinolytic therapy: impact on outcomes in HERO-2
J J Edmond, J K French, P E G Aylward, et al.
The Journal of Pediatrics
|
May 2, 2006
Enzyme replacement therapy for mucopolysaccharidosis VI: a phase 3, randomized, double-blind, placebo-controlled, multinational study of recombinant human N-acetylgalactosamine 4-sulfatase (recombinant human arylsulfatase B or rhASB) and follow-on, open-label extension study
Paul Harmatz, Roberto Giugliani, Ida Schwartz, et al.
Molecular Genetics and Metabolism
|
May 27, 2008
Long-term follow-up of endurance and safety outcomes during enzyme replacement therapy for mucopolysaccharidosis VI: Final results of three clinical studies of recombinant human N-acetylgalactosamine 4-sulfatase
Paul Harmatz, Roberto Giugliani, Ida Vanessa D Schwartz, et al.
Journal of Pediatric Rehabilitation Medicine
|
July 17, 2010
Enzyme replacement therapy for mucopolysaccharidosis VI: Growth and pubertal development in patients treated with recombinant human N-acetylgalactosamine 4-sulfatase
Celeste Decker, Zi-Fan Yu, Roberto Giugliani, et al.
Orphanet Journal of Rare Diseases
|
April 25, 2012
Capturing phenotypic heterogeneity in MPS I: results of an international consensus procedure
Minke H de Ru, Quirine Ga Teunissen, Johanna H van der Lee, et al.
Journal of Inherited Metabolic Disease
|
February 9, 2010
Enzyme replacement therapy for mucopolysaccharidosis VI: evaluation of long-term pulmonary function in patients treated with recombinant human N-acetylgalactosamine 4-sulfatase
Paul Harmatz, Zi-Fan Yu, Roberto Giugliani, et al.
Page
of 11