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BMC Neurology
|
November 8, 2008
Skin-impedance in Fabry Disease: a prospective, controlled, non-randomized clinical study
Surya N Gupta, Markus Ries, Gary J Murray, et al.
Biochemical and Biophysical Research Communications
|
May 29, 2007
Screening for pharmacological chaperones in Fabry disease
Sang-Hoon Shin, Gary J Murray, Stefanie Kluepfel-Stahl, et al.
Pharmacogenetics and Genomics
|
August 14, 2008
Prediction of response of mutated alpha-galactosidase A to a pharmacological chaperone
Sang H Shin, Stefanie Kluepfel-Stahl, Adele M Cooney, et al.
Annals of Neurology
|
March 24, 2005
Convection perfusion of glucocerebrosidase for neuronopathic Gaucher's disease
Russell R Lonser, Stuart Walbridge, Gary J Murray, et al.
Medicine
|
March 13, 2002
Natural history of Fabry renal disease: influence of alpha-galactosidase A activity and genetic mutations on clinical course
Mary H Branton, Raphael Schiffmann, Sharda G Sabnis, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 20, 2004
Bioluminescent imaging of a marking transgene and correction of Fabry mice by neonatal injection of recombinant lentiviral vectors
Makoto Yoshimitsu, Takeya Sato, Kesheng Tao, et al.
Molecular Genetics and Metabolism
|
November 22, 2016
Roscoe Owen Brady, MD: Remembrances of co-investigators and colleagues
Robert J Desnick, Norman W Barton, Scott Furbish, et al.
Pediatrics
|
February 17, 2005
Pediatric Fabry disease
Markus Ries, Surya Gupta, David F Moore, et al.
Molecular Genetics and Metabolism
|
December 17, 2008
Lysosomal Disease Network's "WORLD Symposium 2009". Introduction
Chester B Whitley, John A Barranger, Christine M Eng, et al.
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Search research articles
Search
Showing results (11-20 of 19) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 19 results.
BMC Neurology
|
November 8, 2008
Skin-impedance in Fabry Disease: a prospective, controlled, non-randomized clinical study
Surya N Gupta, Markus Ries, Gary J Murray, et al.
Biochemical and Biophysical Research Communications
|
May 29, 2007
Screening for pharmacological chaperones in Fabry disease
Sang-Hoon Shin, Gary J Murray, Stefanie Kluepfel-Stahl, et al.
Pharmacogenetics and Genomics
|
August 14, 2008
Prediction of response of mutated alpha-galactosidase A to a pharmacological chaperone
Sang H Shin, Stefanie Kluepfel-Stahl, Adele M Cooney, et al.
Annals of Neurology
|
March 24, 2005
Convection perfusion of glucocerebrosidase for neuronopathic Gaucher's disease
Russell R Lonser, Stuart Walbridge, Gary J Murray, et al.
Medicine
|
March 13, 2002
Natural history of Fabry renal disease: influence of alpha-galactosidase A activity and genetic mutations on clinical course
Mary H Branton, Raphael Schiffmann, Sharda G Sabnis, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 20, 2004
Bioluminescent imaging of a marking transgene and correction of Fabry mice by neonatal injection of recombinant lentiviral vectors
Makoto Yoshimitsu, Takeya Sato, Kesheng Tao, et al.
Molecular Genetics and Metabolism
|
November 22, 2016
Roscoe Owen Brady, MD: Remembrances of co-investigators and colleagues
Robert J Desnick, Norman W Barton, Scott Furbish, et al.
Pediatrics
|
February 17, 2005
Pediatric Fabry disease
Markus Ries, Surya Gupta, David F Moore, et al.
Molecular Genetics and Metabolism
|
December 17, 2008
Lysosomal Disease Network's "WORLD Symposium 2009". Introduction
Chester B Whitley, John A Barranger, Christine M Eng, et al.
Page
of 2