Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Katharine B. Harris"'
Autor:
Jennifer N. Kraszewski, Katharine B. Harris, Jill F. Shuger, Michele A. Lloyd-Puryear, Susan A. Berry, Mary Kay Kenney, Coleen A. Boyle, Jill Levy-Fisch, Rani H. Singh, Carol L. Greene, Cynthia A. Cameron
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics
Purpose Treatment of inherited metabolic disorders is accomplished by use of specialized diets employing medical foods and medically necessary supplements. Families seeking insurance coverage for these products express concern that coverage is often
Autor:
John Berninger, Scott D. Grosse, Katharine B. Harris, Michele Caggana, Mary M. Hulihan, Regina Zimmerman, Sanil Thomas, Althea M. Grant, Joseph Kennedy, Ying Wang, Suzette O. Oyeku, Nancy S. Green
Publikováno v:
Genetics in Medicine. 15:222-228
Sickle cell disease is estimated to occur in 1:300–400 African-American births, with higher rates among immigrants from Africa and the Caribbean, and is less common among Hispanic births. This study determined sickle cell disease incidence among Ne
Autor:
Susan A. Berry, Celia I. Kaye, Cynthia F. Hinton, Amy Brower, Anne Marie Comeau, Andrea Williams, Kathryn L. Hassell, Jana Monaco, Bradford L. Therrell, Denise Dougherty, Robert J. Ostrander, Christine Brown, Katharine B. Harris, Lisa Feuchtbaum, Carol L. Greene, Nancy S. Green, Charles J. Homer, Alexis A. Thompson, Alan E. Zuckerman
Publikováno v:
Molecular genetics and metabolism. 118(4)
Newborn screening (NBS) is intended to identify congenital conditions prior to the onset of symptoms in order to provide early intervention that leads to improved outcomes. NBS is a public health success, providing reduction in mortality and improved
Autor:
Fred Lorey, Jill Wallace, Cynthia F. Hinton, Lynette Borgfeld, Roger B. Eaton, Kenneth A. Pass, Bradford L. Therrell, Margaret Drummond-Borg, Katharine B. Harris
Publikováno v:
Pediatrics. 125:S37-S47
Primary congenital hypothyroidism (CH) is a common and preventable cause of intellectual disability. The incidence rate of CH has been reported to be increasing in the United States, but the factors behind the observed rate increase are not known. We
Autor:
Corinna Tempelis, Fred Lorey, Dana C. Crawford, Michele Caggana, Claudia Nash, Katharine B. Harris, Richard S. Olney, Kenneth A. Pass
Publikováno v:
Genetics in Medicine. 4:328-335
Purpose: A population-based cohort from three state newborn screening programs was used to describe β-globin gene cluster variation. Methods: Blood spots from newborns homozygous for HbS were genotyped for five restriction fragment length polymorphi
Autor:
Kenneth A. Pass, Katharine B. Harris
Publikováno v:
Molecular genetics and metabolism. 91(3)
Mandated screening of newborns for congenital hypothyroidism (CH) in NYS was initiated in l978. Currently, every newborn screening program in the U.S. includes CH in its panel. Between 1978 and 2005, 7.4 million newborns were screened for CH in NYS.
Autor:
Kenneth A. Pass, Katharine B. Harris
Publikováno v:
Molecular Genetics and Metabolism. 94:140
Autor:
K Pass, Muin J. Khoury, R Choi, Katharine B. Harris, C Moore, S S Wang, S Kling, R Olne, Fred Lorey
Publikováno v:
Genetics in Medicine. 2:67
Children affected with sickle cell disease (SCD) are at increased risk for morbidity and mortality, especially in the first three years of life. Newborn screening programs for SCD currently operate in over 40 states. To assess the effectiveness of ne