Michele Lloyd-Puryear
Overview
Explore the profile of Michele Lloyd-Puryear including associated specialties, affiliations and a list of published articles.
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22
Citations
431
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Recent Articles
11.
Lloyd-Puryear M, Brower A, Berry S, Brosco J, Bowdish B, Watson M
Genet Med
. 2018 Nov;
21(6):1271-1279.
PMID: 30393376
In the past 20 years, several policy activities were undertaken that shaped today's newborn screening (NBS) programs and their associated NBS research activities: the Newborn Screening Task Force Report; the...
12.
Goldenberg A, Lloyd-Puryear M, Brosco J, Therrell B, Bush L, Berry S, et al.
Genet Med
. 2018 Aug;
21(3):525-533.
PMID: 30100612
Background: 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...
13.
Lin B, Edelman E, McInerney J, OLeary J, Edelson V, Hughes K, et al.
Per Med
. 2018 May;
10(3):307-318.
PMID: 29768747
In the age of genomic medicine, family health history (FHH) remains an important tool for personalized risk assessment as it can inform approaches to disease prevention and management. In primary...
14.
Mendell J, Lloyd-Puryear M
Muscle Nerve
. 2013 May;
48(1):21-6.
PMID: 23716304
This report summarizes the progress made in newborn screening for Duchenne muscular dystrophy (DMD). This subject was discussed fully at a symposium held on September 11-12, 2012, in Bethesda, Maryland,...
15.
Trotter T, Fleischman A, Howell R, Lloyd-Puryear M
Genet Med
. 2011 Mar;
13(4):301-4.
PMID: 21407080
No abstract available.
16.
Gitlin J, Fischbeck K, Crawford T, Cwik V, Fleischman A, Gonye K, et al.
Genet Med
. 2010 Sep;
12(10):621-2.
PMID: 20808230
Spinal muscular atrophy is the most common fatal hereditary disease among newborns and infants. There is as yet no effective treatment. Although a carrier test is available, currently there is...
17.
Calonge N, Green N, Rinaldo P, Lloyd-Puryear M, Dougherty D, Boyle C, et al.
Genet Med
. 2010 Feb;
12(3):153-9.
PMID: 20154628
The Secretary's Advisory Committee on Heritable Disorders in Newborns and Children is charged with evaluating conditions nominated for addition to the uniform screening panel and consequently making recommendations to the...
18.
Kemper A, Boyle C, Aceves J, Dougherty D, Figge J, Fisch J, et al.
Genet Med
. 2008 Apr;
10(4):259-61.
PMID: 18414208
The US Secretary of Health and Human Services' Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children provides guidance to reduce the morbidity and mortality associated with...
19.
Green N, Rinaldo P, Brower A, Boyle C, Dougherty D, Lloyd-Puryear M, et al.
Genet Med
. 2007 Nov;
9(11):792-6.
PMID: 18007148
The Advisory Committee on Heritable Disorders and Genetic Diseases in Newborns and Children is charged with advising the Secretary of the US Department of Health and Human Services in areas...
20.
Kemper A, Hwu W, Lloyd-Puryear M, Kishnani P
Pediatrics
. 2007 Nov;
120(5):e1327-34.
PMID: 17974725
Background: Pompe disease is a lysosomal storage disorder that leads to the accumulation of glycogen and subsequently to muscle weakness, organ damage, and death. Pompe disease is detectable through newborn...