Zobrazeno 1 - 4
of 4
pro vyhledávání: '"R. P. MORSE"'
Autor:
A, Amalfitano, A R, Bengur, R P, Morse, J M, Majure, L E, Case, D L, Veerling, J, Mackey, P, Kishnani, W, Smith, A, McVie-Wylie, J A, Sullivan, G E, Hoganson, J A, Phillips, G B, Schaefer, J, Charrow, R E, Ware, E H, Bossen, Y T, Chen
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 3(2)
Infantile glycogen storage disease type II (GSD-II) is a fatal genetic muscle disorder caused by deficiency of acid alpha-glucosidase (GAA). The purpose of this study was to investigate the safety and efficacy of recombinant human GAA (rhGAA) enzyme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f1b7f6f8f0dc6d3e6e8145518b658dd3
https://pubmed.ncbi.nlm.nih.gov/22878508
https://pubmed.ncbi.nlm.nih.gov/22878508
Autor:
R P, Morse, S, Rockenmacher, R E, Pyeritz, S P, Sanders, F R, Bieber, A, Lin, P, MacLeod, B, Hall, J M, Graham
Publikováno v:
Pediatrics. 86(6)
Marfan syndrome is infrequently diagnosed early in infancy. The experience of the authors with 22 severely affected infants diagnosed as having Marfan syndrome in the first 3 months of life is described and the literature on 32 additional infants wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6f6eb708ee93bbb123fa54bdb0eeb776
https://pubmed.ncbi.nlm.nih.gov/2251026
https://pubmed.ncbi.nlm.nih.gov/2251026
Autor:
R P, Morse
Publikováno v:
Archives of Neurology. 55:1257-1258
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac33906f47a05cc38eb56daca0a20088
https://doi.org/10.1001/archneur.55.9.1257
https://doi.org/10.1001/archneur.55.9.1257