Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Shelley Collins"'
Autor:
Saad K. Anjum, Karna Mangrola, Garrett Fitzpatrick, Kimberly Stockdale, Laura Matthias, Ibne Karim M. Ali, Jennifer R. Cope, Kevin O’Laughlin, Shelley Collins, Stacy G. Beal, Frances M. Saccoccio
Publikováno v:
IDCases, Vol 25, Iss , Pp e01208- (2021)
Primary amebic meningoencephalitis is a rare, usually fatal disease, caused by Naegleria fowleri. This case highlights the challenging clinicopathologic diagnosis in a 13-year-old boy who swam in freshwater in northern Florida where a previous case h
Externí odkaz:
https://doaj.org/article/c8795c4445cc4c958ca7e40e6907fd1e
Autor:
Kimberly Stockdale, Karna Mangrola, Kevin O’Laughlin, Laura Matthias, Stacy G. Beal, Ibne Karim M. Ali, Saad K. Anjum, Frances M. Saccoccio, Garrett Fitzpatrick, Shelley Collins, Jennifer R. Cope
Publikováno v:
IDCases, Vol 25, Iss, Pp e01208-(2021)
IDCases
IDCases
Primary amebic meningoencephalitis is a rare, usually fatal disease, caused by Naegleria fowleri. This case highlights the challenging clinicopathologic diagnosis in a 13-year-old boy who swam in freshwater in northern Florida where a previous case h
Autor:
Kalen Manasco, John Vila, William Bortcosh, Renad Abu-Sawwa, Charles Peloquin, Silvana Carr, Mohammad Alshaer, Shelley Collins, Kathryn DeSear, Barbara Santevecchi, Veena Venugopalan
Publikováno v:
Critical Care Medicine. 50:348-348
Publikováno v:
Medical Science Educator. 27:549-554
Collaborative learning groups have evolved into learning communities at the University of Florida College of Medicine (UF COM) as part of a new integrated curriculum. The article provides an outline of how to develop and use a learning community as a
Autor:
Barbara K. Smith, Barry J. Byrne, Saleem Islam, A. Daniel Martin, Shelley Collins, Jordan Marcus, Lee Ann Lawson, Nadeem I. Shafi, Manuela Corti, Valerie Vernot
Publikováno v:
Experimental Neurology. 287:216-224
Pompe disease is an inherited disorder due to a mutation in the gene that encodes acid α-glucosidase (GAA). Children with infantile-onset Pompe disease develop progressive hypotonic weakness and cardiopulmonary insufficiency that may eventually requ
Autor:
Torrey Baines, Shelley Collins, Daniel Moas, Jennifer Munoz Pareja, Stacy G. Beal, Frances M. Saccoccio, Zasha Francheska Vazquez-Colon, Jose De Cardenas, Natalia Martinez Schlurmann
Publikováno v:
Critical Care Medicine. 49:316-316
Publikováno v:
American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists. 75(22)
Purpose The results of a study to determine if rates of poor response differ in patients receiving continuous nebulized albuterol (CNA) therapy with or without the preservative benzalkonium chloride are presented. Methods A retrospective analysis of
Autor:
Saleem Islam, Cristina Liberati, Roland W. Herzog, Shelley Collins, Lee Ann Lawson, Ibrahim Sacit Tuna, Barry J. Byrne, David D. Fuller, Kirsten E. Coleman, Manuela Corti, Thomas J. Conlon, Barbara K. Smith
Publikováno v:
Human gene therapy. Clinical development. 28(4)
A first-in-human trial of diaphragmatic gene therapy (AAV1-CMV-GAA) to treat respiratory and neural dysfunction in early-onset Pompe disease was conducted. The primary objective of this study was to assess the safety of rAAV1-CMV-hGAA vector delivere
Autor:
Anatole D. Martin, Saleem Islam, Lee Ann Lawson, Brian Cleaver, David D. Fuller, Barbara K. Smith, Cathryn Mah, Thomas J. Conlon, Barry J. Byrne, Nathalie Clement, Nicole Dobjia, Dawn Phillips, Shelley Collins
Publikováno v:
Human Gene Therapy. 24:630-640
Pompe disease is an inherited neuromuscular disease caused by deficiency of lysosomal acid alpha-glucosidase (GAA) leading to glycogen accumulation in muscle and motoneurons. Cardiopulmonary failure in infancy leads to early mortality, and GAA enzyme
Publikováno v:
Hospital pediatrics. 6(7)
In the face of unspeakable tragedy, one can find hope. That is the beginning of the story and the journey at our children’s hospital, which highlights patient centeredness, safety, and quality. In 2012, a child was transferred from an urgent care c