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Pediatrics
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June 1, 2006
California's experience implementing a pilot newborn supplemental screening program using tandem mass spectrometry
Lisa Feuchtbaum, Fred Lorey, Lisa Faulkner, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 5, 2017
Genomic sequencing in cystic fibrosis newborn screening: what works best, two-tier predefined CFTR mutation panels or second-tier CFTR panel followed by third-tier sequencing?
Robert J Currier, Stan Sciortino, Ruiling Liu, et al.
International Journal of Neonatal Screening
|
October 19, 2020
The First Year Experience of Newborn Screening for Pompe Disease in California
Hao Tang, Lisa Feuchtbaum, Stanley Sciortino, et al.
Paediatric and Perinatal Epidemiology
|
February 18, 2015
Undiagnosed metabolic dysfunction and sudden infant death syndrome--a case-control study
Ning An Rosenthal, Robert J Currier, Rebecca J Baer, et al.
Molecular Genetics and Metabolism
|
October 10, 2013
Analysis of cases of 3-methylcrotonyl CoA carboxylase deficiency (3-MCCD) in the California newborn screening program reported in the state database
Christina Lam, Jennifer M Carter, Stephen D Cederbaum, et al.
Pediatrics
|
November 18, 2015
Newborn Screening for Cystic Fibrosis in California
Martin Kharrazi, Juan Yang, Tracey Bishop, et al.
The Journal of Pediatrics
|
July 29, 2023
First Three Years' Experience of Mucopolysaccharidosis Type-I Newborn Screening in California
Toki Fillman, Jamie Matteson, Hao Tang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 1, 2011
What questions should newborn screening long-term follow-up be able to answer? A statement of the US Secretary for Health and Human Services' Advisory Committee on Heritable Disorders in Newborns and Children
Cynthia F Hinton, Lisa Feuchtbaum, Christopher A Kus, et al.
Journal of Neuromuscular Diseases
|
October 24, 2022
California's experience with SMA newborn screening: A successful path to early intervention
Jamie Matteson, Cindy H Wu, Deepika Mathur, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 7, 2013
Developing a public health-tracking system for follow-up of newborn screening metabolic conditions: a four-state pilot project structure and initial findings
Cynthia F Hinton, Cara T Mai, Sarah K Nabukera, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 25) with videos related to
Sort By:
Page
of 3
Pediatrics
|
June 1, 2006
California's experience implementing a pilot newborn supplemental screening program using tandem mass spectrometry
Lisa Feuchtbaum, Fred Lorey, Lisa Faulkner, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 5, 2017
Genomic sequencing in cystic fibrosis newborn screening: what works best, two-tier predefined CFTR mutation panels or second-tier CFTR panel followed by third-tier sequencing?
Robert J Currier, Stan Sciortino, Ruiling Liu, et al.
International Journal of Neonatal Screening
|
October 19, 2020
The First Year Experience of Newborn Screening for Pompe Disease in California
Hao Tang, Lisa Feuchtbaum, Stanley Sciortino, et al.
Paediatric and Perinatal Epidemiology
|
February 18, 2015
Undiagnosed metabolic dysfunction and sudden infant death syndrome--a case-control study
Ning An Rosenthal, Robert J Currier, Rebecca J Baer, et al.
Molecular Genetics and Metabolism
|
October 10, 2013
Analysis of cases of 3-methylcrotonyl CoA carboxylase deficiency (3-MCCD) in the California newborn screening program reported in the state database
Christina Lam, Jennifer M Carter, Stephen D Cederbaum, et al.
Pediatrics
|
November 18, 2015
Newborn Screening for Cystic Fibrosis in California
Martin Kharrazi, Juan Yang, Tracey Bishop, et al.
The Journal of Pediatrics
|
July 29, 2023
First Three Years' Experience of Mucopolysaccharidosis Type-I Newborn Screening in California
Toki Fillman, Jamie Matteson, Hao Tang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 1, 2011
What questions should newborn screening long-term follow-up be able to answer? A statement of the US Secretary for Health and Human Services' Advisory Committee on Heritable Disorders in Newborns and Children
Cynthia F Hinton, Lisa Feuchtbaum, Christopher A Kus, et al.
Journal of Neuromuscular Diseases
|
October 24, 2022
California's experience with SMA newborn screening: A successful path to early intervention
Jamie Matteson, Cindy H Wu, Deepika Mathur, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
December 7, 2013
Developing a public health-tracking system for follow-up of newborn screening metabolic conditions: a four-state pilot project structure and initial findings
Cynthia F Hinton, Cara T Mai, Sarah K Nabukera, et al.
Page
of 3