Publications by authors named "Dawn S Peck"

7Publications

Incorporation of Second-Tier Biomarker Testing Improves the Specificity of Newborn Screening for Mucopolysaccharidosis Type I.

Int J Neonatal Screen 2020 Mar 7;6(1):10. Epub 2020 Feb 7.

Biochemical Genetics Laboratory, Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905, USA; (J.M.L.); (A.L.W.); (G.P.); (A.L.S.); (D.G.); (D.O.); (K.R.); (D.M.); (P.R.).

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March 2020

Surgical septal myectomy for relief of dynamic obstruction in Anderson-Fabry Disease.

Int J Cardiol 2019 10 19;292:91-94. Epub 2019 Jun 19.

Department of Cardiovascular Diseases, Mayo Clinic, Rochester, MN, United States of America. Electronic address:

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October 2019

Cost Efficacy of α-Galactosidase A Enzyme Screening for Fabry Disease.

Mayo Clin Proc 2019 01;94(1):84-88

Department of Cardiovascular Diseases, Mayo Clinic, Rochester, MN; Department of Pediatrics, Division of Pediatric Cardiology, Mayo Clinic, Rochester, MN; Department of Molecular Pharmacology and Experimental Therapeutics, Windland Smith Rice Sudden Death Genomics Laboratory, Mayo Clinic, Rochester, MN.

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January 2019

Fabry disease in infancy and early childhood: a systematic literature review.

Genet Med 2015 May 18;17(5):323-30. Epub 2014 Sep 18.

Division of Human Genetics, Cincinnati Children's Hospital Medical Center, Cincinnati, Missouri, USA.

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May 2015

DNA carrier testing and newborn screening for maple syrup urine disease in Old Order Mennonite communities.

Genet Test Mol Biomarkers 2010 Apr;14(2):205-8

Department of Biochemistry, University of Missouri-Columbia, Columbia, Missouri 65211, USA.

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April 2010