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International Journal of Neonatal Screening
|
October 19, 2020
Duchenne Muscular Dystrophy Newborn Screening, a Case Study for Examining Ethical and Legal Issues for Pilots for Emerging Disorders: Considerations and Recommendations
Michele A Lloyd-Puryear, Thomas O Crawford, Amy Brower, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 16, 2010
Committee report: Method for evaluating conditions nominated for population-based screening of newborns and children
Ned Calonge, Nancy S Green, Piero Rinaldo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 24, 2011
Committee report: Considerations and recommendations for national guidance regarding the retention and use of residual dried blood spot specimens after newborn screening
Bradford L Therrell, W Harry Hannon, Donald B Bailey, et al.
JAMA Neurology
|
May 21, 2019
Maximizing the Benefit of Life-Saving Treatments for Pompe Disease, Spinal Muscular Atrophy, and Duchenne Muscular Dystrophy Through Newborn Screening: Essential Steps
Mei Baker, Robert Griggs, Barry Byrne, et al.
World Journal of Pediatrics : WJP
|
May 4, 2017
Newborn screening for Duchenne muscular dystrophy in China: follow-up diagnosis and subsequent treatment
Qing Ke, Zheng-Yan Zhao, Robert Griggs, et al.
Pediatrics
|
October 12, 2011
Strategies for implementing screening for critical congenital heart disease
Alex R Kemper, William T Mahle, Gerard R Martin, et al.
Journal of Neuromuscular Diseases
|
April 5, 2018
Treatment Algorithm for Infants Diagnosed with Spinal Muscular Atrophy through Newborn Screening
Jacqueline Glascock, Jacinda Sampson, Amanda Haidet-Phillips, et al.
International Journal of Neonatal Screening
|
June 25, 2025
ISNS General Guidelines for Neonatal Bloodspot Screening 2025
Dianne Webster, Amy Gaviglio, Aysha Habib Khan, et al.
Journal of Neuromuscular Diseases
|
February 3, 2020
Revised Recommendations for the Treatment of Infants Diagnosed with Spinal Muscular Atrophy Via Newborn Screening Who Have 4 Copies of SMN2
Jacqueline Glascock, Jacinda Sampson, Anne M Connolly, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 14, 2018
Including ELSI research questions in newborn screening pilot studies
Aaron J Goldenberg, Michele Lloyd-Puryear, Jeffrey P Brosco, et al.
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of 5
Search research articles
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Showing results (31-40 of 46) with videos related to
Sort By:
Page
of 5
International Journal of Neonatal Screening
|
October 19, 2020
Duchenne Muscular Dystrophy Newborn Screening, a Case Study for Examining Ethical and Legal Issues for Pilots for Emerging Disorders: Considerations and Recommendations
Michele A Lloyd-Puryear, Thomas O Crawford, Amy Brower, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
February 16, 2010
Committee report: Method for evaluating conditions nominated for population-based screening of newborns and children
Ned Calonge, Nancy S Green, Piero Rinaldo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 24, 2011
Committee report: Considerations and recommendations for national guidance regarding the retention and use of residual dried blood spot specimens after newborn screening
Bradford L Therrell, W Harry Hannon, Donald B Bailey, et al.
JAMA Neurology
|
May 21, 2019
Maximizing the Benefit of Life-Saving Treatments for Pompe Disease, Spinal Muscular Atrophy, and Duchenne Muscular Dystrophy Through Newborn Screening: Essential Steps
Mei Baker, Robert Griggs, Barry Byrne, et al.
World Journal of Pediatrics : WJP
|
May 4, 2017
Newborn screening for Duchenne muscular dystrophy in China: follow-up diagnosis and subsequent treatment
Qing Ke, Zheng-Yan Zhao, Robert Griggs, et al.
Pediatrics
|
October 12, 2011
Strategies for implementing screening for critical congenital heart disease
Alex R Kemper, William T Mahle, Gerard R Martin, et al.
Journal of Neuromuscular Diseases
|
April 5, 2018
Treatment Algorithm for Infants Diagnosed with Spinal Muscular Atrophy through Newborn Screening
Jacqueline Glascock, Jacinda Sampson, Amanda Haidet-Phillips, et al.
International Journal of Neonatal Screening
|
June 25, 2025
ISNS General Guidelines for Neonatal Bloodspot Screening 2025
Dianne Webster, Amy Gaviglio, Aysha Habib Khan, et al.
Journal of Neuromuscular Diseases
|
February 3, 2020
Revised Recommendations for the Treatment of Infants Diagnosed with Spinal Muscular Atrophy Via Newborn Screening Who Have 4 Copies of SMN2
Jacqueline Glascock, Jacinda Sampson, Anne M Connolly, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 14, 2018
Including ELSI research questions in newborn screening pilot studies
Aaron J Goldenberg, Michele Lloyd-Puryear, Jeffrey P Brosco, et al.
Page
of 5