-
1
-
-
33747591403
-
MS, Mann MY, Lloyd-Puryear MA, Rinaldo P, Howell RR, editors. Newborn screening: toward a uniform screening panel and system.
-
Watson MS, Mann MY, Lloyd-Puryear MA, Rinaldo P, Howell RR, editors. Newborn screening: toward a uniform screening panel and system. Genet Med 2006;8(suppl 1):1S-252S.
-
(2006)
Genet Med
, vol.8
-
-
-
2
-
-
44849139821
-
Expanding newborn screening: process, policy, and priorities.
-
Moyer VA, Calonge N, Teutsch SM, Botkin JR. Expanding newborn screening: process, policy, and priorities. Hastings Cent Rep 2008;38:32-39.
-
(2008)
Hastings Cent Rep
, vol.38
, pp. 32-39
-
-
Moyer, V.A.1
Calonge, N.2
Teutsch, S.M.3
Botkin, J.R.4
-
3
-
-
33646843914
-
We need expanded newborn screening.
-
Howell RR. We need expanded newborn screening. Pediatrics 2006;117:1800-1805.
-
(2006)
Pediatrics
, vol.117
, pp. 1800-1805
-
-
Howell, R.R.1
-
4
-
-
33646853843
-
Newborn screening technology: proceed with caution.
-
Botkin JR, Clayton EW, Fost NC, et al. Newborn screening technology: proceed with caution. Pediatrics 2006;117:1793-1799.
-
(2006)
Pediatrics
, vol.117
, pp. 1793-1799
-
-
Botkin, J.R.1
Clayton, E.W.2
Fost, N.C.3
-
5
-
-
33744814955
-
American Academy of Pediatrics Newborn Screening Task Force Recommendations: how far have we come?
-
Lloyd-Puryear MA, Tonniges T, Van Dyck PC, et al. American Academy of Pediatrics Newborn Screening Task Force Recommendations: how far have we come? Pediatrics 2006;117:S194-S211.
-
(2006)
Pediatrics
, vol.117
-
-
Lloyd-Puryear, M.A.1
Tonniges, T.2
Van Dyck, P.C.3
-
6
-
-
36249029975
-
Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children. Committee report: advancing the current recommended panel of conditions for newborn screening.
-
Green NS, Rinaldo P, Brower A, et al; Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children. Committee report: advancing the current recommended panel of conditions for newborn screening. Genet Med 2007;9:792-796.
-
(2007)
Genet Med
, vol.9
, pp. 792-796
-
-
Green, N.S.1
Rinaldo, P.2
Brower, A.3
-
7
-
-
85026167580
-
-
Available at: http://www.cdc.gov/genomics/gtesting/EGAPP/index.htm. Accessed January 9, 2009.
-
Available at: http://www.cdc.gov/genomics/gtesting/EGAPP/index.htm. Accessed January 9, 2009.
-
-
-
-
8
-
-
0035318124
-
Current methods of the US Preventive Services Task Force: a review of the process.
-
Methods Work Group, Third US Preventive Services Task Force. Current methods of the US Preventive Services Task Force: a review of the process. Am J Prev Med 2001;20:21-35.
-
(2001)
Am J Prev Med
, vol.20
, pp. 21-35
-
-
-
9
-
-
34547099816
-
Current processes of the US Preventive Services Task Force: refining evidence-based recommendation development.
-
Guirguis-Blake J, Calonge N, Miller T, Siu A, Teutsch S, Whitlock E; U.S. Preventive Services Task Force. Current processes of the US Preventive Services Task Force: refining evidence-based recommendation development. Ann Intern Med 2007;147:117-122.
-
(2007)
Ann Intern Med
, vol.147
, pp. 117-122
-
-
Guirguis-Blake, J.1
Calonge, N.2
Miller, T.3
Siu, A.4
Teutsch, S.5
Whitlock, E.6
-
10
-
-
0018178436
-
Problems of spectrum and bias in evaluating the efficacy of diagnostic tests.
-
Ransohoff DF, Feinstein AR. Problems of spectrum and bias in evaluating the efficacy of diagnostic tests. N Engl J Med 1978;299:926-930.
-
(1978)
N Engl J Med
, vol.299
, pp. 926-930
-
-
Ransohoff, D.F.1
Feinstein, A.R.2
-
11
-
-
85026157516
-
-
See Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children, minutes of meeting 10, “Process for nominating and evaluating conditions for inclusion on the uniform newborn screening panel.” Available at: http://www.hrsa.gov/heritabledisorderscommittee/meetings/2007may/minutes0507.htmc. Accessed August 1, 2009.
-
See Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children, minutes of meeting 10, “Process for nominating and evaluating conditions for inclusion on the uniform newborn screening panel.” Available at: http://www.hrsa.gov/heritabledisorderscommittee/meetings/2007may/minutes0507.htmc. Accessed August 1, 2009.
-
-
-
-
12
-
-
33845972665
-
Making the case for objective performance metrics in newborn screening by tandem mass spectrometry.
-
Rinaldo P, Zafari S, Tortorelli S, Matern D. Making the case for objective performance metrics in newborn screening by tandem mass spectrometry. Ment Retard Dev Disabil Res Rev 2006;12:255-261.
-
(2006)
Ment Retard Dev Disabil Res Rev
, vol.12
, pp. 255-261
-
-
Rinaldo, P.1
Zafari, S.2
Tortorelli, S.3
Matern, D.4
-
13
-
-
33845968875
-
Pilot programs in newborn screening.
-
Pass K, Green N, Lorey F, Sherwin J, Comeau AM. Pilot programs in newborn screening. Ment Retard Dev Disabil Res Rev 2006;12:4:293- 300.
-
(2006)
Ment Retard Dev Disabil Res Rev
, vol.12
, Issue.4
, pp. 293-300
-
-
Pass, K.1
Green, N.2
Lorey, F.3
Sherwin, J.4
Comeau, A.M.5
-
14
-
-
85026160325
-
-
NHS Center for Reviews and Dissemination March 2001. Accessed October 17, 2008.
-
NHS Center for Reviews and Dissemination March 2001. Accessed October 17, 2008.
-
-
-
-
15
-
-
17344383506
-
Clinical effectiveness and cost-effectiveness of neonatal screening for inborn errors of metabolism using tandem mass spectrometry: a systematic review.
-
Pandor A, Eastham J, Beverley C, Chilcott J, Paisley S. Clinical effectiveness and cost-effectiveness of neonatal screening for inborn errors of metabolism using tandem mass spectrometry: a systematic review. Health Technol Assess 2004;8:12.
-
(2004)
Health Technol Assess
, vol.8
, pp. 12
-
-
Pandor, A.1
Eastham, J.2
Beverley, C.3
Chilcott, J.4
Paisley, S.5
-
16
-
-
17144470109
-
Neonatal screening for inborn errors of metabolism: cost, yield and outcome.
-
Pollitt RJ, Green A, McCabe CJ, et al. Neonatal screening for inborn errors of metabolism: cost, yield and outcome. Health Technol Assess 1997;1:i-iv, 1-202.
-
(1997)
Health Technol Assess
, vol.1
-
-
Pollitt, R.J.1
Green, A.2
McCabe, C.J.3
-
17
-
-
85026157401
-
-
See Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children, Committee Reports. Available at: http://www.hrsa.gov/heritabledisorderscommittee/reports/, listed as KrabbeEvidenceReviewFinalDraft.pdf, evidencereviewSCID/default.htm, evidenceReviewPompeOct2008.htm. Accessed October 1, 2009.
-
See Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children, Committee Reports. Available at: http://www.hrsa.gov/heritabledisorderscommittee/reports/, listed as KrabbeEvidenceReviewFinalDraft.pdf, evidencereviewSCID/default.htm, evidenceReviewPompeOct2008.htm. Accessed October 1, 2009.
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