BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

187 related articles for article (PubMed ID: 19059852)

  • 1. Questioning the consensus: managing carrier status results generated by newborn screening.
    Miller FA; Robert JS; Hayeems RZ
    Am J Public Health; 2009 Feb; 99(2):210-5. PubMed ID: 19059852
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical obligations and public health programmes: healthcare provider reasoning about managing the incidental results of newborn screening.
    Miller FA; Hayeems RZ; Bombard Y; Little J; Carroll JC; Wilson B; Allanson J; Paynter M; Bytautas JP; Christensen R; Chakraborty P
    J Med Ethics; 2009 Oct; 35(10):626-34. PubMed ID: 19793944
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genetic Counselors' Experience with and Opinions on the Management of Newborn Screening Incidental Carrier Findings.
    Leppert K; Bisordi K; Nieto J; Maloney K; Guan Y; Dixon S; Egense A
    J Genet Couns; 2018 Dec; 27(6):1328-1340. PubMed ID: 29687313
    [TBL] [Abstract][Full Text] [Related]  

  • 4. To know or not to know, disclosure of a newborn carrier screening test result for cystic fibrosis.
    Vernooij-van Langen AM; Reijntjens S; van der Pal SM; Loeber JG; Dompeling E; Dankert-Roelse JE
    Eur J Med Genet; 2013 Apr; 56(4):192-6. PubMed ID: 23352994
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Disclosing to parents newborn carrier status identified by routine blood spot screening.
    Oliver S; Dezateux C; Kavanagh J; Lempert T; Stewart R
    Cochrane Database Syst Rev; 2004 Oct; (4):CD003859. PubMed ID: 15495068
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Parents' responses to receiving sickle cell or cystic fibrosis carrier results for their child following newborn screening.
    Ulph F; Cullinan T; Qureshi N; Kai J
    Eur J Hum Genet; 2015 Apr; 23(4):459-65. PubMed ID: 25005733
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Managing misaligned paternity findings in research including sickle cell disease screening in Kenya: 'consulting communities' to inform policy.
    Marsh V; Kombe F; Fitzpatrick R; Molyneux S; Parker M
    Soc Sci Med; 2013 Nov; 96():192-9. PubMed ID: 24034967
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Communication of carrier status information following universal newborn screening for sickle cell disorders and cystic fibrosis: qualitative study of experience and practice.
    Kai J; Ulph F; Cullinan T; Qureshi N
    Health Technol Assess; 2009 Nov; 13(57):1-82, iii. PubMed ID: 19948087
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical and ethical considerations in managing carrier detection.
    Ross LF; Clayton EW
    Am J Public Health; 2009 Aug; 99(8):1348-9. PubMed ID: 19542030
    [No Abstract]   [Full Text] [Related]  

  • 10. The ethics of deception in biomedical research.
    Sharpe G; Weisstub DN
    Health Law Can; 1996 May; 16(4):101-10. PubMed ID: 10173418
    [No Abstract]   [Full Text] [Related]  

  • 11. A systematic review of the effects of disclosing carrier results generated through newborn screening.
    Hayeems RZ; Bytautas JP; Miller FA
    J Genet Couns; 2008 Dec; 17(6):538-49. PubMed ID: 18956236
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic screening and ethics: European perspectives.
    Chadwick R; ten Have H; Husted J; Levitt M; McGleenan T; Shickle D; Wiesing U
    J Med Philos; 1998 Jun; 23(3):255-73. PubMed ID: 9736188
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Challenging the Current Recommendations for Carrier Testing in Children.
    VanNoy GE; Genetti CA; McGuire AL; Green RC; Beggs AH; Holm IA;
    Pediatrics; 2019 Jan; 143(Suppl 1):S27-S32. PubMed ID: 30600268
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Carrier detection and clinical uncertainty: the case for public health ethics.
    Miller FA; Hayeems RZ; Robert JS
    Am J Public Health; 2009 Aug; 99(8):1349-50. PubMed ID: 19542029
    [No Abstract]   [Full Text] [Related]  

  • 15. [Genomic newborn screening. Perspective from the Ethics Commission of the Spanish Society for Human Genetics. Part II: Ethical, legal and social issues (ELSIs) of the introduction of next generation sequencing technologies in a public health newborn screening program.].
    Pàmpols Ros T; Pérez Aytés A; García Sagredo JM; Díaz de Bustamante A; Blanco Guillermo I
    Rev Esp Salud Publica; 2022 Mar; 96():. PubMed ID: 35283479
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic counseling and neonatal screening for cystic fibrosis: an assessment of the communication process.
    Ciske DJ; Haavisto A; Laxova A; Rock LZ; Farrell PM
    Pediatrics; 2001 Apr; 107(4):699-705. PubMed ID: 11335747
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Implementing carrier screening for cystic fibrosis outside the clinic: ethical analysis in the light of the personalist view.
    Di Pietro ML; Teleman AA; Gonzalez-Melado FJ; Zace D; Di Raimo FR; Lucidi V; Refolo P
    Clin Ter; 2018; 169(2):e71-e76. PubMed ID: 29595869
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Informed choice and public health screening for children: the case of blood spot screening.
    Hargreaves KM; Stewart RJ; Oliver SR
    Health Expect; 2005 Jun; 8(2):161-71. PubMed ID: 15860056
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Ethical questions concerning newborn genetic screening.
    Esquerda M; Palau F; Lorenzo D; Cambra FJ; Bofarull M; Cusi V; Interdisciplinar En Bioetica G
    Clin Genet; 2021 Jan; 99(1):93-98. PubMed ID: 32779199
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Imparting carrier status results detected by universal newborn screening for sickle cell and cystic fibrosis in England: a qualitative study of current practice and policy challenges.
    Parker H; Qureshi N; Ulph F; Kai J
    BMC Health Serv Res; 2007 Dec; 7():203. PubMed ID: 18078504
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.