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Pediatrics
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December 5, 2003
The Maternal Phenylketonuria Project: a summary of progress and challenges for the future
Joe 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 disease
Joe 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 policy
Joe T R Clarke
Drugs
|
December 8, 2007
Treatment of lysosomal storage disorders : progress with enzyme replacement therapy
Marianne Rohrbach, Joe T R Clarke
Journal of Inherited Metabolic Disease
|
June 28, 2006
Ornithine transcarbamoylase deficiency presenting with acute liver failure
Ahlam 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 disease
Chantal F Morel, Joe T R Clarke
Molecular Neurobiology
|
August 4, 2005
Enzyme replacement therapy of Fabry disease
Joe T R Clarke, R Mark Iwanochko
Journal of Cutaneous Medicine and Surgery
|
September 14, 2012
Erythropoietic protoporphyria: spectrum of three cases
Janie 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 disease
Fatma Al-Jasmi, Laura Moldovan, Joe T R Clarke
Page
of 7
Search research articles
Search
Showing results (1-10 of 67) with videos related to
Sort By:
Page
of 7
Pediatrics
|
December 5, 2003
The Maternal Phenylketonuria Project: a summary of progress and challenges for the future
Joe 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 disease
Joe 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 policy
Joe T R Clarke
Drugs
|
December 8, 2007
Treatment of lysosomal storage disorders : progress with enzyme replacement therapy
Marianne Rohrbach, Joe T R Clarke
Journal of Inherited Metabolic Disease
|
June 28, 2006
Ornithine transcarbamoylase deficiency presenting with acute liver failure
Ahlam 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 disease
Chantal F Morel, Joe T R Clarke
Molecular Neurobiology
|
August 4, 2005
Enzyme replacement therapy of Fabry disease
Joe T R Clarke, R Mark Iwanochko
Journal of Cutaneous Medicine and Surgery
|
September 14, 2012
Erythropoietic protoporphyria: spectrum of three cases
Janie 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 disease
Fatma Al-Jasmi, Laura Moldovan, Joe T R Clarke
Page
of 7