Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Harris Naemi"'
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 12, Pp n/a-n/a (2019)
Abstract Background Fragile X syndrome (FXS) is the most common inherited form of intellectual disability. Many providers offer preconception or prenatal FXS carrier screening. However, guidelines recommend screening only for those with a family hist
Externí odkaz:
https://doaj.org/article/254a09885edf47c59ce8cdf2227ae2d0
Autor:
Duy K. Duong, Salma Shariff-Marco, Iona Cheng, Harris Naemi, Lisa M. Moy, Robert Haile, Baldeep Singh, Ann Leung, Ann Hsing, Viswam S. Nair
Publikováno v:
Preventive Medicine Reports, Vol 6, Iss C, Pp 17-22 (2017)
Low dose CT (LDCT) for lung cancer screening is an evidence-based, guideline recommended, and Medicare approved test but uptake requires further study. We therefore conducted patient and provider surveys to elucidate factors associated with utilizati
Externí odkaz:
https://doaj.org/article/2ccd24d87930473aa4583776db7868f7
Autor:
Ann N. Leung, Ann W. Hsing, Lisa M. Moy, Harris Naemi, Viswam S. Nair, Iona Cheng, Robert W. Haile, Salma Shariff-Marco, Baldeep Singh, Duy K. Duong
Publikováno v:
Preventive Medicine Reports, Vol 6, Iss C, Pp 17-22 (2017)
Preventive Medicine Reports
Preventive Medicine Reports
Low dose CT (LDCT) for lung cancer screening is an evidence-based, guideline recommended, and Medicare approved test but uptake requires further study. We therefore conducted patient and provider surveys to elucidate factors associated with utilizati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5b4da62bbb210f54e6e4e3e26c1d6cc
http://www.sciencedirect.com/science/article/pii/S221133551730013X
http://www.sciencedirect.com/science/article/pii/S221133551730013X
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 7, Iss 12, Pp n/a-n/a (2019)
Molecular Genetics & Genomic Medicine, Vol 7, Iss 12, Pp n/a-n/a (2019)
Background Fragile X syndrome (FXS) is the most common inherited form of intellectual disability. Many providers offer preconception or prenatal FXS carrier screening. However, guidelines recommend screening only for those with a family history or un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4086b8b93eb471c0a5ec86a49607ce1
http://europepmc.org/articles/PMC6900367
http://europepmc.org/articles/PMC6900367
Publikováno v:
Fertility and Sterility. 112:e261-e262
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c70aa57c27d415e3b16a91e2a3eb236
https://doi.org/10.1016/j.fertnstert.2019.07.789
https://doi.org/10.1016/j.fertnstert.2019.07.789
Publikováno v:
Chest. 150:733A
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::953e2238a901bdca144589ea414fe87c
https://doi.org/10.1016/j.chest.2016.08.828
https://doi.org/10.1016/j.chest.2016.08.828