Zobrazeno 1 - 4
of 4
pro vyhledávání: '"J G, Quinlan"'
Autor:
J G, Quinlan, D, Cambier, S, Lyden, A, Dalvi, R K, Upputuri, P, Gartside, S E, Michaels, D, Denman
Publikováno v:
Musclenerve. 20(8)
We have refined the mdx mouse as a clinical model for Duchenne dystrophy. Our power estimates, primary measures, regular sacrifice intervals, and quality checks constitute a high-speed, low-cost system for preclinically testing therapies designed to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1221926d9223c9e3735bd8c90b5b6a83
https://pubmed.ncbi.nlm.nih.gov/9236793
https://pubmed.ncbi.nlm.nih.gov/9236793
Autor:
F J, Samaha, J G, Quinlan
Publikováno v:
Journal of child neurology. 11(1)
The purpose of this review is to analyze the clinical applications of a remarkable series of advances made in molecular genetics, primarily with regard to Becker muscular dystrophy. A new classification is required to clarify such syndromes as Duchen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::83df878941409d88c7186222fc5190f6
https://pubmed.ncbi.nlm.nih.gov/8745379
https://pubmed.ncbi.nlm.nih.gov/8745379
Autor:
M S, Nussbaum, G J, Rosenthal, F J, Samaha, H T, Grinvalsky, J G, Quinlan, M, Schmerler, J E, Fischer
Publikováno v:
Surgery. 112(4)
Thymectomy has continued to gain acceptance as definitive treatment for myasthenia gravis. Because of the nature of thymic embryology with scattered rests throughout the anterior mediastinum, we advocate a transsternal thymectomy with extended anteri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::952dd74048eb48b791879a5673a62ba2
https://pubmed.ncbi.nlm.nih.gov/1411938
https://pubmed.ncbi.nlm.nih.gov/1411938
Publikováno v:
Musclenerve. 13(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c7ce7089267bc3e56de252bc8b42f7ea
https://pubmed.ncbi.nlm.nih.gov/2320049
https://pubmed.ncbi.nlm.nih.gov/2320049