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Journal of Inherited Metabolic Disease
|
November 8, 2003
Prenatal diagnosis for arginase deficiency: a case study
S 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 centre
H C Glass, A Feigenbaum, J T R Clarke
Journal of Inherited Metabolic Disease
|
July 9, 2009
Experience with the treatment of argininosuccinic aciduria during pregnancy
L Reid, E Perreault, G Lafrance, et al.
Journal of Inherited Metabolic Disease
|
January 27, 2005
Gaucher disease: variability in phenotype among siblings
D 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 A
C 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 literature
A 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 disease
C 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 Survey
A 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 initiative
S 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 Initiative
S Sirrs, J T R Clarke, D G Bichet, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 14) with videos related to
Sort By:
Page
of 2
Journal of Inherited Metabolic Disease
|
November 8, 2003
Prenatal diagnosis for arginase deficiency: a case study
S 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 centre
H C Glass, A Feigenbaum, J T R Clarke
Journal of Inherited Metabolic Disease
|
July 9, 2009
Experience with the treatment of argininosuccinic aciduria during pregnancy
L Reid, E Perreault, G Lafrance, et al.
Journal of Inherited Metabolic Disease
|
January 27, 2005
Gaucher disease: variability in phenotype among siblings
D 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 A
C 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 literature
A 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 disease
C 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 Survey
A 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 initiative
S 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 Initiative
S Sirrs, J T R Clarke, D G Bichet, et al.
Page
of 2