Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Chris Hendriksz"'
Autor:
Roberto Giugliani, Uma Ramaswami, Anna Tylki‐Szymańska, Barbara K. Burton, James Davison, Chris Hendriksz, Young Bae Sohn, Paul Harmatz, Erin Jozwiak, Torayuki Okuyama, Adriana M. Montaño, William S. Sly, Barbara Triggs‐Raine, Promita Ghosh, Marvin Natowicz
Publikováno v:
Lysosomal Storage Disorders. :155-193
Autor:
Chris Hendriksz, Atul Mehta
Publikováno v:
Lysosomal Storage Disorders. :295-298
Autor:
Christian J, Hendriksz, Roberto, Giugliani, Paul, Harmatz, Christina, Lampe, Ana Maria, Martins, Gregory M, Pastores, Robert D, Steiner, Elisa, Leão Teles, Vassili, Valayannopoulos, Chris, Hendriksz
Publikováno v:
Journal of Inherited Metabolic Disease. 36:373-384
To outline the design, baseline data, and 5-year follow-up data of patients with mucopolysaccharidosis (MPS) VI enrolled in the Clinical Surveillance Program (CSP), a voluntary, multinational, observational program.The MPS VI CSP was opened in 2005 t
Autor:
Shunji Tomatsu, Chris Hendriksz, Paul Harmatz, Michael Beck, Jones Simon, Tim Wood, Ralph Lachman, Tadao Orii
Publikováno v:
Molecular Genetics and Metabolism. 108:S90-S91
Publikováno v:
British Journal of Nursing. 18:321-322
Hunter syndrome (mucopolysaccharidosis type II) is a rare lysosomal storage disease caused by a deficiency of the lysosomal enzyme iduronate-2-sulphatase and the subsequent progressive cellular accumulation of glycosaminoglycans. Children with this d
Publikováno v:
Endocrine Abstracts. :1-1
Publikováno v:
Pediatric Research. 61:134-134