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J E Wraith

Showing results (1-10 of 115) with videos related to

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Developmental Medicine and Child Neurology|September 26, 2001
Advances in the treatment of lysosomal storage diseaseJ E Wraith
Journal of Inherited Metabolic Disease|June 19, 2001
Enzyme replacement therapy in mucopolysaccharidosis type I: progress and emerging difficultiesJ E Wraith
Journal of Inherited Metabolic Disease|January 1, 1996
Non-kinetic hyperglycinaemia: prolonged survival in a patient with a mild variantJ E Wraith
Archives of Disease in Childhood|October 1, 1992
Diagnosis and management of inborn errors of metabolism--an updateJ E Wraith
International Journal of Clinical Pharmacology and Therapeutics|December 31, 2009
Enzyme replacement therapy for the management of the mucopolysaccharidosesJ E Wraith
Archives of Disease in Childhood|October 1, 1989
Diagnosis and management of inborn errors of metabolismJ E Wraith
Archives of Disease in Childhood|December 22, 2000
Ornithine carbamoyltransferase deficiencyJ E Wraith
Archives of Disease in Childhood|March 1, 1995
The mucopolysaccharidoses: a clinical review and guide to managementJ E Wraith
Seminars in Neonatology : SN|June 19, 2002
Lysosomal disordersJ E Wraith
Journal of Inherited Metabolic Disease|June 10, 2006
Limitations of enzyme replacement therapy: current and futureJ E Wraith
Pageof 12

Showing results (1-10 of 115) with videos related to

Sort By:
Pageof 12
Developmental Medicine and Child Neurology|September 26, 2001
Advances in the treatment of lysosomal storage diseaseJ E Wraith
Journal of Inherited Metabolic Disease|June 19, 2001
Enzyme replacement therapy in mucopolysaccharidosis type I: progress and emerging difficultiesJ E Wraith
Journal of Inherited Metabolic Disease|January 1, 1996
Non-kinetic hyperglycinaemia: prolonged survival in a patient with a mild variantJ E Wraith
Archives of Disease in Childhood|October 1, 1992
Diagnosis and management of inborn errors of metabolism--an updateJ E Wraith
International Journal of Clinical Pharmacology and Therapeutics|December 31, 2009
Enzyme replacement therapy for the management of the mucopolysaccharidosesJ E Wraith
Archives of Disease in Childhood|October 1, 1989
Diagnosis and management of inborn errors of metabolismJ E Wraith
Archives of Disease in Childhood|December 22, 2000
Ornithine carbamoyltransferase deficiencyJ E Wraith
Archives of Disease in Childhood|March 1, 1995
The mucopolysaccharidoses: a clinical review and guide to managementJ E Wraith
Seminars in Neonatology : SN|June 19, 2002
Lysosomal disordersJ E Wraith
Journal of Inherited Metabolic Disease|June 10, 2006
Limitations of enzyme replacement therapy: current and futureJ E Wraith
Pageof 12