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
1.
Maloney B, Park S, Sowizral M, Brackett I, Moslehi R, Chung W, et al.
Clin Biochem
. 2023 Jul;
118:110614.
PMID: 37479106
Introduction: Newborn screening for Duchenne muscular dystrophy can be performed via a first-tier creatine kinase-MM measurement followed by reflex testing to second-tier molecular analysis of the DMD gene. In order...
2.
Piel F, Rees D, DeBaun M, Nnodu O, Ranque B, Thompson A, et al.
Lancet Haematol
. 2023 Jul;
10(8):e633-e686.
PMID: 37451304
No abstract available.
3.
Tavakoli N, Gruber D, Armstrong N, Chung W, Maloney B, Park S, et al.
Ann Clin Transl Neurol
. 2023 Jun;
10(8):1383-1396.
PMID: 37350320
Objective: Duchenne muscular dystrophy (DMD) is an X-linked disorder resulting in progressive muscle weakness and atrophy, cardiomyopathy, and in late stages, cardiorespiratory impairment, and death. As treatments for DMD have...
4.
Gruber D, Lloyd-Puryear M, Armstrong N, Scavina M, Tavakoli N, Brower A, et al.
Am J Med Genet C Semin Med Genet
. 2022 Sep;
190(2):197-205.
PMID: 36152336
Duchenne muscular dystrophy (DMD) is the most common pediatric-onset form of muscular dystrophy, occurring in 1 in 5,000 live male births. DMD is a multi-system disease resulting in muscle weakness...
5.
Chung W, Berg J, Botkin J, Brenner S, Brosco J, Brothers K, et al.
Am J Med Genet C Semin Med Genet
. 2022 Jul;
190(2):222-230.
PMID: 35838066
In the US, newborn screening (NBS) is a unique health program that supports health equity and screens virtually every baby after birth, and has brought timely treatments to babies since...
6.
Boudar Z, Sehli S, El Janahi S, Al Idrissi N, Hamdi S, Dini N, et al.
Front Pediatr
. 2022 Jul;
10:886627.
PMID: 35799697
Early infancy is critical for the development of an infant's gut flora. Many factors can influence microbiota development during the pre- and postnatal periods, including maternal factors, antibiotic exposure, mode...
7.
Timonen A, Lloyd-Puryear M, Hougaard D, Merio L, Makinen P, Laitala V, et al.
Int J Neonatal Screen
. 2020 Oct;
5(3):27.
PMID: 33072986
Duchenne muscular dystrophy (DMD/Duchenne) is a progressive X-linked disease and is the most common pediatric-onset form of muscular dystrophy, affecting approximately 1:5000 live male births. DNA testing for mutations in...
8.
Al-Zaidy S, Lloyd-Puryear M, Kennedy A, Lopez V, Mendell J
Int J Neonatal Screen
. 2019 Oct;
3(2):8.
PMID: 31588416
Duchenne muscular dystrophy (DMD) is the most common childhood form of muscular dystrophy, with an estimated frequency of 1:5000 live births. The impact of the disease presents as early as...
9.
Kaye C, Bodurtha J, Edick M, Ginsburg S, Keehn A, Lloyd-Puryear M, et al.
Genet Med
. 2019 Sep;
22(1):241.
PMID: 31551579
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
10.
Kaye C, Bodurtha J, Edick M, Ginsburg S, Keehn A, Lloyd-Puryear M, et al.
Genet Med
. 2019 Sep;
22(2):381-388.
PMID: 31488898
Purpose: To outline structures for regional genetic services support centers that improve access to clinical genetic services. Methods: A workgroup (WG) and advisory committee (AC) (1) conducted a comprehensive review...