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J T R Clarke

Showing results (1-10 of 14) with videos related to

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Journal of Inherited Metabolic Disease|November 8, 2003
Prenatal diagnosis for arginase deficiency: a case studyS Hewson, J T R Clarke, S Cederbaum
Journal of Inherited Metabolic Disease|April 8, 2006
A study on the nature of genetic metabolic practice at a major paediatric referral centreH C Glass, A Feigenbaum, J T R Clarke
Journal of Inherited Metabolic Disease|July 9, 2009
Experience with the treatment of argininosuccinic aciduria during pregnancyL Reid, E Perreault, G Lafrance, et al.
Journal of Inherited Metabolic Disease|January 27, 2005
Gaucher disease: variability in phenotype among siblingsD Amato, T Stachiw, J T R Clarke, et al.
Journal of Inherited Metabolic Disease|October 26, 2007
Unsuccessful treatment attempt: cord blood stem cell transplantation in a patient with Niemann-Pick disease type AC F Morel, A Gassas, J Doyle, et al.
Bone Marrow Transplantation|July 3, 2003
Life-threatening pulmonary hemorrhages post bone marrow transplantation in Hurler syndrome. Report of three cases and review of the literatureA Gassas, L Sung, J J Doyle, et al.
Journal of Inherited Metabolic Disease|January 27, 2009
Proposed high-risk screening protocol for Fabry disease in patients with renal and vascular diseaseC Auray-Blais, D S Millington, S P Young, et al.
Journal of Medical Genetics|May 29, 2009
Natural course of Fabry disease: changing pattern of causes of death in FOS - Fabry Outcome SurveyA Mehta, J T R Clarke, R Giugliani, et al.
Molecular Genetics and Metabolism|February 19, 2014
Outcomes of patients treated through the Canadian Fabry disease initiativeS M Sirrs, D G Bichet, R Casey, et al.
Molecular Genetics and Metabolism|December 22, 2009
Baseline characteristics of patients enrolled in the Canadian Fabry Disease InitiativeS Sirrs, J T R Clarke, D G Bichet, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Journal of Inherited Metabolic Disease|November 8, 2003
Prenatal diagnosis for arginase deficiency: a case studyS Hewson, J T R Clarke, S Cederbaum
Journal of Inherited Metabolic Disease|April 8, 2006
A study on the nature of genetic metabolic practice at a major paediatric referral centreH C Glass, A Feigenbaum, J T R Clarke
Journal of Inherited Metabolic Disease|July 9, 2009
Experience with the treatment of argininosuccinic aciduria during pregnancyL Reid, E Perreault, G Lafrance, et al.
Journal of Inherited Metabolic Disease|January 27, 2005
Gaucher disease: variability in phenotype among siblingsD Amato, T Stachiw, J T R Clarke, et al.
Journal of Inherited Metabolic Disease|October 26, 2007
Unsuccessful treatment attempt: cord blood stem cell transplantation in a patient with Niemann-Pick disease type AC F Morel, A Gassas, J Doyle, et al.
Bone Marrow Transplantation|July 3, 2003
Life-threatening pulmonary hemorrhages post bone marrow transplantation in Hurler syndrome. Report of three cases and review of the literatureA Gassas, L Sung, J J Doyle, et al.
Journal of Inherited Metabolic Disease|January 27, 2009
Proposed high-risk screening protocol for Fabry disease in patients with renal and vascular diseaseC Auray-Blais, D S Millington, S P Young, et al.
Journal of Medical Genetics|May 29, 2009
Natural course of Fabry disease: changing pattern of causes of death in FOS - Fabry Outcome SurveyA Mehta, J T R Clarke, R Giugliani, et al.
Molecular Genetics and Metabolism|February 19, 2014
Outcomes of patients treated through the Canadian Fabry disease initiativeS M Sirrs, D G Bichet, R Casey, et al.
Molecular Genetics and Metabolism|December 22, 2009
Baseline characteristics of patients enrolled in the Canadian Fabry Disease InitiativeS Sirrs, J T R Clarke, D G Bichet, et al.
Pageof 2