Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Bradford Therrell"'
Autor:
Martin Kharrazi, Charlene Sacramento, Anne Comeau, Jaime Hale, Michele Caggana, Denise Kay, Rachel Lee, Brendan Reilly, John Thompson, Samya Nasr, Mary Kleyn, Gary Hoffman, Mei Baker, Colleen Clarke, Cheryl Harris, M. Dorley, Hilary Fryman, Ankit Sutaria, Amy Hietala, Holly Winslow, Holly Richards, Bradford Therrell
Publikováno v:
International Journal of Neonatal Screening; Volume 8; Issue 4; Pages: 58
Testing immunoreactive trypsinogen (IRT) is the first step in cystic fibrosis (CF) newborn screening. While high IRT is associated with CF, some cases are missed. This survey aimed to find factors associated with missed CF cases due to IRT levels bel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e714ca4cbd8d2ace7694883a90dd800
https://pubmed.ncbi.nlm.nih.gov/36412584
https://pubmed.ncbi.nlm.nih.gov/36412584
Publikováno v:
International Journal of Neonatal Screening. 8:37
Dr [...]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ea175dc5dd031adf9856e51a0a572a3
https://doi.org/10.3390/ijns8020037
https://doi.org/10.3390/ijns8020037
Autor:
Aaron J, Goldenberg, Michele, Lloyd-Puryear, Jeffrey P, Brosco, Bradford, Therrell, Lynn, Bush, Susan, Berry, Amy, Brower, Natasha, Bonhomme, Bruce, Bowdish, Denise, Chrysler, Angus, Clarke, Thomas, Crawford, Edward, Goldman, Sally, Hiner, R Rodney, Howell, David, Orren, Benjamin S, Wilfond, Michael, Watson
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics. 21(3)
The evidence review processes for adding new conditions to state newborn screening (NBS) panels rely on data from pilot studies aimed at assessing the potential benefits and harms of screening. However, the consideration of ethical, legal, and social
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::51118008ef32307368166677be17062c
https://pubmed.ncbi.nlm.nih.gov/30100612
https://pubmed.ncbi.nlm.nih.gov/30100612
Autor:
Bradford Therrell
Publikováno v:
Seminars in Perinatology. 39:169-170
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f2bdd2a312c37c138fd4311b6bb00f0
https://doi.org/10.1053/j.semperi.2015.03.001
https://doi.org/10.1053/j.semperi.2015.03.001
Publikováno v:
The Southeast Asian journal of tropical medicine and public health. 34
Disorders of fatty acid oxidation and organic acid metabolism produce serious clinical problems including death. Introduction of MS/MS technology for newborn screening allowed detection of these disorders in a single process, more than doubling the n
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::926e6de210c7fc21e25822329d1803e9
https://pubmed.ncbi.nlm.nih.gov/15906714
https://pubmed.ncbi.nlm.nih.gov/15906714
A comparative cost analysis of newborn screening for classic congenital adrenal hyperplasia in Texas
Autor:
Brosnan, C. A., Brosnan, P., Bradford Therrell, Slater, C. H., Swint, J. M., Annegers, J. F., Riley, W. J.
Publikováno v:
Scopus-Elsevier
OBJECTIVE: Texas mandates a two-test newborn screening program for congenital adrenal hyperplasia (CAH): one test at birth and a second test at approximately one to two weeks after birth. The authors compared the dollar cost of detecting infants with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::2ee918b9761dd9769ca86e8d81c2a919
https://europepmc.org/articles/PMC1308657/
https://europepmc.org/articles/PMC1308657/
Autor:
Songya Pang, Anastasia Clark, Eurico Camargo Neto, Roberto Giugliani, Heather Dean, Jeremy Winter, Jean-Louis Dhondt, J.P Farriaux, Annette Graters, Emanuele Cacciari, Antonio Balsamo, Sandro Piazzi, Seizo Suwa, Yusuhiro Kuroda, Yoshiro Wada, Hiroshi Naruse, T Kizaki, N Ichihara, Osamu Arai, S Harada, Kenji Fujieda, Nobuo Matsuura, Satoshi Kusuda, Masaru Fukushi, Yoshikiyo Mizushima, Y Kikuti, Takio Yoyoura, Sumitaka Saisho, Kazukiko Shimozawa, Masaru Matsumoto, Dianne Webster, Laura Vilarinho, A.M Wallace, Iñaki Eguileor, I Marzana, Elena Dulin Iñiguez, A Fernandez Sanchez, C Gonzalez Gallego, Lars Hagenfeldt, Claes Guthenberg, Ulrika von Dobeln, Astrid Thilen, Agne Larsson, T Torresani, Christy LeBlond, Christine Papadea, Frank Rumph, Willie Craft, Sydney Kling, Eva Tsalikian, Jennifer Cook, J Getchell, J Susanin, Marvin Mitchell, Lindsay Hofman, Edwin Naylor, Bradford Therrell, Lois Brown, Linda Prentice, Michael Glass, Sheila Neier
Publikováno v:
Scopus-Elsevier
Congenital adrenal hyperplasia (CAH) due to 21-hydroxylase deficiency can be detected by newborn screening. The screening alone in 29 programs from 13 countries resulted in the diagnosis of CAH in 1 2 of affected newborns and expedited the diagnosis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::883667a276eab67ffc93e0cf430b6ad6
http://www.scopus.com/inward/record.url?eid=2-s2.0-0027317014&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0027317014&partnerID=MN8TOARS