Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Jenifer Gentle"'
Autor:
Alison H. Howie, Kylie Tingley, Michal Inbar-Feigenberg, John J. Mitchell, Kim Angel, Jenifer Gentle, Maureen Smith, Martin Offringa, Nancy J. Butcher, Philippe M. Campeau, Pranesh Chakraborty, Alicia Chan, Dean Fergusson, Eva Mamak, Peyton McClelland, Saadet Mercimek-Andrews, Aizeddin Mhanni, Zeinab Moazin, Cheryl Rockman-Greenberg, C. Anthony Rupar, Becky Skidmore, Sylvia Stockler, Kednapa Thavorn, Alexandra Wyatt, Beth K. Potter, INFORM RARE Network
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-15 (2024)
Abstract Background To inform the development of a core outcome set (COS) for children and youth with mucopolysaccharidoses (MPS), we aimed to identify all outcomes and associated outcome measurement instruments that are reported in recent clinical t
Externí odkaz:
https://doaj.org/article/3f5faa2b5e894b579d9b0f0a9ed05831
Autor:
Alison H. Howie, Kylie Tingley, Michal Inbar-Feigenberg, John J. Mitchell, Nancy J. Butcher, Martin Offringa, Maureen Smith, Kim Angel, Jenifer Gentle, Alexandra Wyatt, Philippe M. Campeau, Alicia Chan, Pranesh Chakraborty, Farah El Turk, Eva Mamak, Aizeddin Mhanni, Becky Skidmore, Rebecca Sparkes, Sylvia Stockler, Beth K. Potter, in collaboration with the INFORM RARE Network
Publikováno v:
Trials, Vol 22, Iss 1, Pp 1-11 (2021)
Abstract Background Mucopolysaccharidoses (MPS) are a group of inherited metabolic diseases characterized by chronic, progressive multi-system manifestations with varying degrees of severity. Disease-modifying therapies exist to treat some types of M
Externí odkaz:
https://doaj.org/article/57f0bc46d0ab4e048db0a236ad6299b8
Autor:
Alison H. Howie, Kylie Tingley, Michal Inbar-Feigenberg, John J. Mitchell, Nancy J. Butcher, Martin Offringa, Maureen Smith, Kim Angel, Jenifer Gentle, Alexandra Wyatt, Philippe M. Campeau, Alicia Chan, Pranesh Chakraborty, Farah El Turk, Eva Mamak, Aizeddin Mhanni, Becky Skidmore, Rebecca Sparkes, Sylvia Stockler, Beth K. Potter, in collaboration with the INFORM RARE Network
Publikováno v:
Trials, Vol 22, Iss 1, Pp 1-1 (2021)
Externí odkaz:
https://doaj.org/article/4e45347f368f4cd3bf5cabb416165f8e
Autor:
Alexandra Wyatt, Michal Inbar-Feigenberg, Aizeddin A. Mhanni, Kim Angel, Pranesh Chakraborty, Jenifer Gentle, Alison H. Howie, Beth K. Potter, Philippe M. Campeau, Rebecca Sparkes, Farah El Turk, Maureen Smith, Martin Offringa, John J. Mitchell, Sylvia Stockler, Kylie Tingley, Nancy J. Butcher, Becky Skidmore, Eva Mamak, Alicia Chan
Publikováno v:
Trials, Vol 22, Iss 1, Pp 1-11 (2021)
Trials
Trials
Background Mucopolysaccharidoses (MPS) are a group of inherited metabolic diseases characterized by chronic, progressive multi-system manifestations with varying degrees of severity. Disease-modifying therapies exist to treat some types of MPS; howev
Autor:
Alison H. Howie, Alexandra Wyatt, Michal Inbar-Feigenberg, John J. Mitchell, Maureen Smith, Kim Angel, Jenifer Gentle, Nancy J. Butcher, Martin Offringa, Philippe M. Campeau, Alicia K. Chan, Pranesh Chakraborty, Andrea Chow, Farah El Turk, Cheryl R. Greenberg, Eva Mamak, Aziz Mhanni, Tony Rupar, Rebecca Sparkes, Kednapa Thavorn, Kylie Tingley, Beth K. Potter
Publikováno v:
Molecular Genetics and Metabolism. 138:107154