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Results: 1 to 20 of 102

1.

What questions should newborn screening long-term follow-up be able to answer? A statement of the US Secretary for Health and Human Services' Advisory Committee on Heritable Disorders in Newborns and Children.

Hinton CF, Feuchtbaum L, Kus CA, Kemper AR, Berry SA, Levy-Fisch J, Luedtke J, Kaye C, Boyle CA.

Genet Med. 2011 Oct;13(10):861-5. doi: 10.1097/GIM.0b013e3182209f09.

PMID:
21716119
[PubMed - indexed for MEDLINE]
2.

Long-term follow-up after diagnosis resulting from newborn screening: statement of the US Secretary of Health and Human Services' Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children.

Kemper AR, Boyle CA, Aceves J, Dougherty D, Figge J, Fisch JL, Hinman AR, Greene CL, Kus CA, Miller J, Robertson D, Telfair J, Therrell B, Lloyd-Puryear M, van Dyck PC, Howell RR.

Genet Med. 2008 Apr;10(4):259-61. doi: 10.1097/GIM.0b013e31816b64f9. Erratum in: Genet Med. 2008 May;10(5):368. Telfair, Joseph [added].

PMID:
18414208
[PubMed - indexed for MEDLINE]
3.

Including the initial newborn screening bloodspot collection device serial number on birth certificates: basis and recommendations from the Secretary of Health and Human Services' Advisory Committee on Heritable Disorders in Newborns and Children.

Therrell BL, Wu C; Secretary of Health and Human Services Advisory Committee on Heritable Disorders in Newborns and Children; SACHDNC Subcommittee on Long Term Follow-up and Treatment.

Genet Med. 2013 Mar;15(3):229-33. doi: 10.1038/gim.2012.121. Epub 2012 Oct 4.

PMID:
23037933
[PubMed - indexed for MEDLINE]
4.

From developing guidelines to implementing legislation: actions of the US Advisory Committee on Heritable Disorders in Newborns and Children toward advancing and improving newborn screening.

Howell RR, Lloyd-Puryear MA.

Semin Perinatol. 2010 Apr;34(2):121-4. doi: 10.1053/j.semperi.2009.12.004.

PMID:
20207261
[PubMed - indexed for MEDLINE]
5.
6.

Committee report: Considerations and recommendations for national guidance regarding the retention and use of residual dried blood spot specimens after newborn screening.

Therrell BL Jr, Hannon WH, Bailey DB Jr, Goldman EB, Monaco J, Norgaard-Pedersen B, Terry SF, Johnson A, Howell RR.

Genet Med. 2011 Jul;13(7):621-4. doi: 10.1097/GIM.0b013e3182147639.

PMID:
21602691
[PubMed - indexed for MEDLINE]
7.

Good laboratory practices for biochemical genetic testing and newborn screening for inherited metabolic disorders.

Centers for Disease Control and Prevention (CDC).

MMWR Recomm Rep. 2012 Apr 6;61(RR-2):1-44.

PMID:
22475884
[PubMed - indexed for MEDLINE]
Free Article
8.

Newborn dried bloodspot screening: mapping the clinical and public health components and activities.

Hinman AR, Mann MY, Singh RH; NDBS Business Process Analysis Workgroup.

Genet Med. 2009 Jun;11(6):418-24. doi: 10.1097/GIM.0b013e31819f1b33. Erratum in: Genet Med. 2009 Aug;11(8):594.

PMID:
19369886
[PubMed - indexed for MEDLINE]
9.

The context and approach for the California newborn screening short- and long-term follow-up data system: preliminary findings.

Feuchtbaum L, Dowray S, Lorey F.

Genet Med. 2010 Dec;12(12 Suppl):S242-50. doi: 10.1097/GIM.0b013e3181fe5d66.

PMID:
21150370
[PubMed - indexed for MEDLINE]
10.

Advisory committee on heritable disorders and genetic diseases in newborns and children.

Howell RR; Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children.

Ment Retard Dev Disabil Res Rev. 2006;12(4):313-5. No abstract available.

PMID:
17183571
[PubMed - indexed for MEDLINE]
11.

Long-term follow-up in newborn screening: A systems approach for improving health outcomes.

Lloyd-Puryear MA, Brower A.

Genet Med. 2010 Dec;12(12 Suppl):S256-60. doi: 10.1097/GIM.0b013e3181fe5d9c.

PMID:
21150372
[PubMed - indexed for MEDLINE]
12.

Committee Report: advancing the current recommended panel of conditions for newborn screening.

Green NS, Rinaldo P, Brower A, Boyle C, Dougherty D, Lloyd-Puryear M, Mann MY, Howell RR; Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children.

Genet Med. 2007 Nov;9(11):792-6.

PMID:
18007148
[PubMed - indexed for MEDLINE]
13.

Long-term follow-up of children with confirmed newborn screening disorders using record linkage.

Wang Y, Caggana M, Sango-Jordan M, Sun M, Druschel CM.

Genet Med. 2011 Oct;13(10):881-6. doi: 10.1097/GIM.0b013e31821e485b.

PMID:
21637103
[PubMed - indexed for MEDLINE]
14.

Assuring clinical genetic services for newborns identified through U.S. newborn screening programs.

Kaye CI, Livingston J, Canfield MA, Mann MY, Lloyd-Puryear MA, Therrell BL Jr.

Genet Med. 2007 Aug;9(8):518-27.

PMID:
17700390
[PubMed - indexed for MEDLINE]
15.

Long-term follow-up to ensure quality care of individuals diagnosed with newborn screening conditions: early experience in New England.

Sahai I, Eaton RB, Hale JE, Mulcahy EA, Comeau AM.

Genet Med. 2010 Dec;12(12 Suppl):S220-7. doi: 10.1097/GIM.0b013e3181fe5d37.

PMID:
21150368
[PubMed - indexed for MEDLINE]
16.

Impact of expanded newborn screening--United States, 2006.

Centers for Disease Control and Prevention (CDC).

MMWR Morb Mortal Wkly Rep. 2008 Sep 19;57(37):1012-5.

PMID:
18802410
[PubMed - indexed for MEDLINE]
Free Article
17.

Committee report: Method for evaluating conditions nominated for population-based screening of newborns and children.

Calonge N, Green NS, Rinaldo P, Lloyd-Puryear M, Dougherty D, Boyle C, Watson M, Trotter T, Terry SF, Howell RR; Advisory Committee on Heritable Disorders in Newborns and Children.

Genet Med. 2010 Mar;12(3):153-9. doi: 10.1097/GIM.0b013e3181d2af04.

PMID:
20154628
[PubMed - indexed for MEDLINE]
18.

Newborn dried bloodspot screening: long-term follow-up activities and information system requirements.

Singh RH, Hinman AR.

Genet Med. 2010 Dec;12(12 Suppl):S261-6. doi: 10.1097/GIM.0b013e3181fe5f6c.

PMID:
21150373
[PubMed - indexed for MEDLINE]
19.

Secretary's Advisory Committee on Heritable Disorders in Newborns and Children response to the President's Council on Bioethics report: the changing moral focus of newborn screening.

Trotter TL, Fleischman AR, Howell RR, Lloyd-Puryear M; Secretary's Advisory Committee on Heritable Disorders in Newborns and Children.

Genet Med. 2011 Apr;13(4):301-4. doi: 10.1097/GIM.0b013e318210655d. No abstract available.

PMID:
21407080
[PubMed - indexed for MEDLINE]
20.

Examination of the communication practices between state newborn screening programs and the medical home.

Kim S, Lloyd-Puryear MA, Tonniges TF.

Pediatrics. 2003 Feb;111(2):E120-6.

PMID:
12563084
[PubMed - indexed for MEDLINE]

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