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Joe T R Clarke

Showing results (1-10 of 67) with videos related to

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Pediatrics|December 5, 2003
The Maternal Phenylketonuria Project: a summary of progress and challenges for the futureJoe T R Clarke
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|April 19, 2005
[How to cope with new challenges in the diagnosis and management of inborn errors of metabolism]Joe T R Clarke
Annals of Internal Medicine|March 21, 2007
Narrative review: Fabry diseaseJoe T R Clarke
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|January 18, 2006
Is the current approach to reviewing new drugs condemning the victims of rare diseases to death? A call for a national orphan drug review policyJoe T R Clarke
Drugs|December 8, 2007
Treatment of lysosomal storage disorders : progress with enzyme replacement therapyMarianne Rohrbach, Joe T R Clarke
Journal of Inherited Metabolic Disease|June 28, 2006
Ornithine transcarbamoylase deficiency presenting with acute liver failureAhlam Mustafa, Joe T R Clarke
Expert Opinion on Biological Therapy|April 17, 2009
The use of agalsidase alfa enzyme replacement therapy in the treatment of Fabry diseaseChantal F Morel, Joe T R Clarke
Molecular Neurobiology|August 4, 2005
Enzyme replacement therapy of Fabry diseaseJoe T R Clarke, R Mark Iwanochko
Journal of Cutaneous Medicine and Surgery|September 14, 2012
Erythropoietic protoporphyria: spectrum of three casesJanie Bertrand, Joe T R Clarke, Dominique Hanna
BMC Medical Education|October 27, 2010
Hunter disease eClinic: interactive, computer-assisted, problem-based approach to independent learning about a rare genetic diseaseFatma Al-Jasmi, Laura Moldovan, Joe T R Clarke
Pageof 7

Showing results (1-10 of 67) with videos related to

Sort By:
Pageof 7
Pediatrics|December 5, 2003
The Maternal Phenylketonuria Project: a summary of progress and challenges for the futureJoe T R Clarke
Zhonghua Er Ke Za Zhi = Chinese Journal of Pediatrics|April 19, 2005
[How to cope with new challenges in the diagnosis and management of inborn errors of metabolism]Joe T R Clarke
Annals of Internal Medicine|March 21, 2007
Narrative review: Fabry diseaseJoe T R Clarke
CMAJ : Canadian Medical Association Journal = Journal De L'Association Medicale Canadienne|January 18, 2006
Is the current approach to reviewing new drugs condemning the victims of rare diseases to death? A call for a national orphan drug review policyJoe T R Clarke
Drugs|December 8, 2007
Treatment of lysosomal storage disorders : progress with enzyme replacement therapyMarianne Rohrbach, Joe T R Clarke
Journal of Inherited Metabolic Disease|June 28, 2006
Ornithine transcarbamoylase deficiency presenting with acute liver failureAhlam Mustafa, Joe T R Clarke
Expert Opinion on Biological Therapy|April 17, 2009
The use of agalsidase alfa enzyme replacement therapy in the treatment of Fabry diseaseChantal F Morel, Joe T R Clarke
Molecular Neurobiology|August 4, 2005
Enzyme replacement therapy of Fabry diseaseJoe T R Clarke, R Mark Iwanochko
Journal of Cutaneous Medicine and Surgery|September 14, 2012
Erythropoietic protoporphyria: spectrum of three casesJanie Bertrand, Joe T R Clarke, Dominique Hanna
BMC Medical Education|October 27, 2010
Hunter disease eClinic: interactive, computer-assisted, problem-based approach to independent learning about a rare genetic diseaseFatma Al-Jasmi, Laura Moldovan, Joe T R Clarke
Pageof 7