Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Terry B. White"'
Publikováno v:
Neumología Pediátrica. 13:72-74
En algunos casos el diagnóstico de fibrosis quística (FQ) aún constituye un desafío. Con el tiempo la genética de esta enfermedad se ha ido aclarando y por otro lado se cuenta con tamizaje neonatal, lo que ha provocado reconsiderar los criterios
Autor:
Terry B. White, Philip M. Farrell
Publikováno v:
The Journal of Pediatrics. 181:S1-S3
Autor:
Bruce C. Marshall, Kevin W Southern, Susanna A. McColley, Nico Derichs, Frank J. Accurso, Michael J. Rock, Patrick R. Sosnay, Philip M. Farrell, Michelle S. Howenstine, Terry B. White, Margaret Rosenfeld, Sarah E. Hempstead, Clement L. Ren, Isabelle Sermet-Gaudelus
Publikováno v:
JOURNAL OF PEDIATRICS
Objective Cystic fibrosis (CF), caused by mutations in the CF transmembrane conductance regulator ( CFTR ) gene, continues to present diagnostic challenges. Newborn screening and an evolving understanding of CF genetics have prompted a reconsideratio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ab71ce30ef18d52007719f303c7b321
Autor:
Terry B. White, Carlo Castellani, Karen S. Raraigh, Patrick R. Sosnay, Emmanuelle Girodon, Philip M. Farrell, Clement L. Ren, Danieli Salinas
Publikováno v:
The Journal of pediatrics.
Objective As a Mendelian disease, genetics plays an integral role in the diagnosis of cystic fibrosis (CF). The identification of 2 disease-causing mutations in the CF transmembrane conductance regulator (CFTR) in an individual with a phenotype provi
Objective Because cystic fibrosis (CF) can be difficult to diagnose, and because information about the genetic complexities and pathologic basis of the disease has grown so rapidly over the decades, several consensus conferences have been held by the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6df23dc573248db86c52be7f3e5d37b
http://hdl.handle.net/11562/981404
http://hdl.handle.net/11562/981404
Autor:
Randall L. Rosenblatt, Daniel Rosenbluth, Marcia Katz, Henry L. Dorkin, Patrick A. Flume, Moira L. Aitken, Michelle S. Howenstine, Manu Jain, David C. McGiffin, Joseph M. Pilewski, Ahmet Uluer, Craig W. Lillehei, Beryl J. Rosenstein, Hector H. Gutierrez, Terry B. White, James D. Acton, Randall K. Young, Thomas M. Egan, Kathryn A. Sabadosa, Steven Strausbaugh, Mary K Lester, Sally E. Mitchell, Douglas S. Holsclaw, Bruce C. Marshall, Mike Mulligan, David M. Orenstein, Donna Beth Willey-Courand, Peter J. Mogayzel, Susanna A. McColley, Souheil Saddekni, Melissa Chin, Lynne M. Quittell, Paul Mohabir, Christopher M. Oermann, James R. Yankaskas, Michael P. Boyle, Robert J. Kuhn, R. Duane Davis, Jill Fleige, Michael J. Rock, Elizabeth Tullis, Anne M Downs, James L. Cunningham, Peter J Murphy, John L. Colombo, Linda L. Wolfenden, Thomas W. Ferkol, Patricia M. Joseph, Jeffrey S. Wagener, George Z. Retsch-Bogart, Christopher H. Goss, Karen A. Robinson, Carlos Milla, Felix Ratjen, Michael S. Schechter, Patricia E. Burrows, Aruna Sannuti, Charles B. Huddleston, Robert L. Vender, Leslie Hazle, Mark J. Sands, Charles T. Burke, Wickii T. Vigneswaran, Ronald C. Rubenstein, Guillermo A. doPico, Jerry A. Nick, Wyn Hoover, Mark H. Wholey
Publikováno v:
American Journal of Respiratory and Critical Care Medicine. 182:298-306
Cystic fibrosis (CF) is a recessive genetic disease characterized by dehydration of the airway surface liquid and impaired mucociliary clearance. As a result, individuals with the disease have difficulty clearing pathogens from the lung and experienc
Autor:
Karen A. Robinson, Richard B. Parad, Suzanne H. Michel, Drucy Borowitz, Frank J. Accurso, Bruce C. Marshall, Margaret Rosenfeld, Philip M. Farrell, Terry B. White, Stephanie D. Davis, Stephanie L. Spear, Kathryn A. Sabadosa
Publikováno v:
The Journal of Pediatrics. 155:S73-S93
Newborn screening for cystic fibrosis (CF) offers the opportunity for early medical and nutritional intervention that can lead to improved outcomes. Management of the asymptomatic infant diagnosed with CF through newborn screening, prenatal diagnosis
Autor:
Carlo Castellani, Philip M. Farrell, Peter R. Durie, Garry R. Cutting, Terry B. White, Beryl J. Rosenstein, Frank J. Accurso, John Massie, Michael J. Rock, Vicky A. LeGrys, Preston W. Campbell, Richard B. Parad
Publikováno v:
The Journal of Pediatrics. 153:S4-S14
Newborn screening (NBS) for cystic fibrosis (CF) is increasingly being implemented and is soon likely to be in use throughout the United States, because early detection permits access to specialized medical care and improves outcomes. The diagnosis o
Autor:
Terry B. White, Ronald J. Sokol, Carroll E. Cross, André M. Cantin, Henry Jay Forman, Drucy Borowitz
Publikováno v:
Free Radical Biology and Medicine. 42:15-31
Although great strides are being made in the care of individuals with cystic fibrosis (CF), this condition remains the most common fatal hereditary disease in North America. Numerous links exist between progression of CF lung disease and oxidative st
Autor:
Robert M. Aris, Sarah L. Elkin, Elizabeth Tullis, Theresa A. Guise, Micheal P. Boyle, Nelson B. Watts, Drucy Borowitz, Laura K. Bachrach, Terry B. White, Dana S. Hardin, Patricia M. Joseph, Peter A. Merkel, Michael F. Holick, Charles S. Haworth, Kimberly O. O'Brien
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 90:1888-1896
Cystic fibrosis (CF) is the most common genetic disease within the Caucasian population and leads to premature respiratory failure. Approximately 60,000 individuals are currently living with CF in North America and Europe, 40% of whom are adults. The