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C M Eng

Showing results (31-40 of 35) with videos related to

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Journal of Inherited Metabolic Disease|March 10, 2007
Fabry disease: baseline medical characteristics of a cohort of 1765 males and females in the Fabry RegistryC M Eng, J Fletcher, W R Wilcox, et al.
Molecular Genetics and Metabolism|November 26, 2008
Expanded clinical and molecular spectrum of guanidinoacetate methyltransferase (GAMT) deficiencyS U Dhar, F Scaglia, F-Y Li, et al.
American Journal of Human Genetics|February 17, 2001
A phase 1/2 clinical trial of enzyme replacement in fabry disease: pharmacokinetic, substrate clearance, and safety studiesC M Eng, M Banikazemi, R E Gordon, et al.
Pediatrics|November 11, 2009
Multidisciplinary management of Hunter syndromeJoseph Muenzer, M Beck, C M Eng, et al.
Clinical and Experimental Immunology|July 22, 2014
Vaccine-associated varicella and rubella infections in severe combined immunodeficiency with isolated CD4 lymphocytopenia and mutations in IL7R detected by tandem whole exome sequencing and chromosomal microarrayD K Bayer, C A Martinez, H S Sorte, et al.
Pageof 4

Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
Journal of Inherited Metabolic Disease|March 10, 2007
Fabry disease: baseline medical characteristics of a cohort of 1765 males and females in the Fabry RegistryC M Eng, J Fletcher, W R Wilcox, et al.
Molecular Genetics and Metabolism|November 26, 2008
Expanded clinical and molecular spectrum of guanidinoacetate methyltransferase (GAMT) deficiencyS U Dhar, F Scaglia, F-Y Li, et al.
American Journal of Human Genetics|February 17, 2001
A phase 1/2 clinical trial of enzyme replacement in fabry disease: pharmacokinetic, substrate clearance, and safety studiesC M Eng, M Banikazemi, R E Gordon, et al.
Pediatrics|November 11, 2009
Multidisciplinary management of Hunter syndromeJoseph Muenzer, M Beck, C M Eng, et al.
Clinical and Experimental Immunology|July 22, 2014
Vaccine-associated varicella and rubella infections in severe combined immunodeficiency with isolated CD4 lymphocytopenia and mutations in IL7R detected by tandem whole exome sequencing and chromosomal microarrayD K Bayer, C A Martinez, H S Sorte, et al.
Pageof 4