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Lisa Feuchtbaum

Showing results (11-20 of 25) with videos related to

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Pediatrics|June 1, 2006
California's experience implementing a pilot newborn supplemental screening program using tandem mass spectrometryLisa 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 CaliforniaHao 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 studyNing 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 databaseChristina Lam, Jennifer M Carter, Stephen D Cederbaum, et al.
Pediatrics|November 18, 2015
Newborn Screening for Cystic Fibrosis in CaliforniaMartin 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 CaliforniaToki 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 ChildrenCynthia 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 interventionJamie 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 findingsCynthia F Hinton, Cara T Mai, Sarah K Nabukera, et al.
Pageof 3

Showing results (11-20 of 25) with videos related to

Sort By:
Pageof 3
Pediatrics|June 1, 2006
California's experience implementing a pilot newborn supplemental screening program using tandem mass spectrometryLisa 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 CaliforniaHao 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 studyNing 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 databaseChristina Lam, Jennifer M Carter, Stephen D Cederbaum, et al.
Pediatrics|November 18, 2015
Newborn Screening for Cystic Fibrosis in CaliforniaMartin 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 CaliforniaToki 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 ChildrenCynthia 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 interventionJamie 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 findingsCynthia F Hinton, Cara T Mai, Sarah K Nabukera, et al.
Pageof 3