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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 Cutaneous Medicine and Surgery
|
September 14, 2012
Erythropoietic protoporphyria: spectrum of three cases
Janie Bertrand, Joe T R Clarke, Dominique Hanna
The Journal of Steroid Biochemistry and Molecular Biology
|
June 1, 1995
The murine 3 beta-hydroxysteroid dehydrogenase multigene family: structure, function and tissue-specific expression
A H Payne, T R Clarke, P A Bain
Nursing Homes
|
April 12, 1978
Make "paper care" demonstrate patient care
T R Clarke, W L Distasi, C J Wallace
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
BMC Medical Education
|
October 27, 2010
Hunter disease eClinic: interactive, computer-assisted, problem-based approach to independent learning about a rare genetic disease
Fatma Al-Jasmi, Laura Moldovan, Joe T R Clarke
Health & Social Work
|
February 1, 1978
Developing a multidisciplinary conference
T R Clarke, W L Distasi, C J Wallace
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.
The West Indian Medical Journal
|
March 2, 2011
A possible case of spinal tuberculosis in a HIV-positive male
T R Clarke, G Barrow, D T Gilbert, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 21, 2007
The pharmacology of multiple regimens of agalsidase alfa enzyme replacement therapy for Fabry disease
Joe T R Clarke, Michael L West, Jan Bultas, et al.
Page
of 12
Search research articles
Search
Showing results (21-30 of 119) with videos related to
Sort By:
Page
of 12
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 Cutaneous Medicine and Surgery
|
September 14, 2012
Erythropoietic protoporphyria: spectrum of three cases
Janie Bertrand, Joe T R Clarke, Dominique Hanna
The Journal of Steroid Biochemistry and Molecular Biology
|
June 1, 1995
The murine 3 beta-hydroxysteroid dehydrogenase multigene family: structure, function and tissue-specific expression
A H Payne, T R Clarke, P A Bain
Nursing Homes
|
April 12, 1978
Make "paper care" demonstrate patient care
T R Clarke, W L Distasi, C J Wallace
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
BMC Medical Education
|
October 27, 2010
Hunter disease eClinic: interactive, computer-assisted, problem-based approach to independent learning about a rare genetic disease
Fatma Al-Jasmi, Laura Moldovan, Joe T R Clarke
Health & Social Work
|
February 1, 1978
Developing a multidisciplinary conference
T R Clarke, W L Distasi, C J Wallace
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.
The West Indian Medical Journal
|
March 2, 2011
A possible case of spinal tuberculosis in a HIV-positive male
T R Clarke, G Barrow, D T Gilbert, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 21, 2007
The pharmacology of multiple regimens of agalsidase alfa enzyme replacement therapy for Fabry disease
Joe T R Clarke, Michael L West, Jan Bultas, et al.
Page
of 12