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Fred Lorey

Showing results (31-40 of 41) with videos related to

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Birth Defects Research. Part A, Clinical and Molecular Teratology|May 30, 2013
A pilot study using residual newborn dried blood spots to assess the potential role of cytomegalovirus and Toxoplasma gondii in the etiology of congenital hydrocephalusRegina M Simeone, Sonja A Rasmussen, Joanne V Mei, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 1, 2010
Effect of specimen storage conditions on newborn dried blood spots used to assess Toxoplasma gondii immunoglobulin M (IgM)Joanne V Mei, LiXia Li, Sonja A Rasmussen, et al.
Molecular Genetics and Metabolism|May 9, 2009
Newborn screening for X-linked adrenoleukodystrophy (X-ALD): validation of a combined liquid chromatography-tandem mass spectrometric (LC-MS/MS) methodWalter C Hubbard, Ann B Moser, Anita C Liu, et al.
Molecular Genetics and Metabolism|March 20, 2012
Biochemical, molecular, and clinical characteristics of children with short chain acyl-CoA dehydrogenase deficiency detected by newborn screening in CaliforniaNatalie M Gallant, Karen Leydiker, Hao Tang, et al.
Epidemiology (Cambridge, Mass.)|April 20, 2002
DNA banking for epidemiologic studies: a review of current practicesKaren Steinberg, Jeanne Beck, Deborah Nickerson, et al.
The Journal of Pediatrics|April 17, 2010
Two-tier approach to the newborn screening of methylenetetrahydrofolate reductase deficiency and other remethylation disorders with tandem mass spectrometrySilvia Tortorelli, Coleman T Turgeon, James S Lim, et al.
The Journal of Allergy and Clinical Immunology|July 2, 2013
Newborn screening for severe combined immunodeficiency and T-cell lymphopenia in California: results of the first 2 yearsAntonia Kwan, Joseph A Church, Morton J Cowan, et al.
International Journal of Neonatal Screening|August 18, 2020
A Comparative Effectiveness Study of Newborn Screening Methods for Four Lysosomal Storage DisordersKaren A Sanders, Dimitar K Gavrilov, Devin Oglesbee, et al.
JAMA|August 21, 2014
Newborn screening for severe combined immunodeficiency in 11 screening programs in the United StatesAntonia Kwan, Roshini S Abraham, Robert Currier, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 7, 2012
Enhanced interpretation of newborn screening results without analyte cutoff valuesGregg Marquardt, Robert Currier, David M S McHugh, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
Birth Defects Research. Part A, Clinical and Molecular Teratology|May 30, 2013
A pilot study using residual newborn dried blood spots to assess the potential role of cytomegalovirus and Toxoplasma gondii in the etiology of congenital hydrocephalusRegina M Simeone, Sonja A Rasmussen, Joanne V Mei, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 1, 2010
Effect of specimen storage conditions on newborn dried blood spots used to assess Toxoplasma gondii immunoglobulin M (IgM)Joanne V Mei, LiXia Li, Sonja A Rasmussen, et al.
Molecular Genetics and Metabolism|May 9, 2009
Newborn screening for X-linked adrenoleukodystrophy (X-ALD): validation of a combined liquid chromatography-tandem mass spectrometric (LC-MS/MS) methodWalter C Hubbard, Ann B Moser, Anita C Liu, et al.
Molecular Genetics and Metabolism|March 20, 2012
Biochemical, molecular, and clinical characteristics of children with short chain acyl-CoA dehydrogenase deficiency detected by newborn screening in CaliforniaNatalie M Gallant, Karen Leydiker, Hao Tang, et al.
Epidemiology (Cambridge, Mass.)|April 20, 2002
DNA banking for epidemiologic studies: a review of current practicesKaren Steinberg, Jeanne Beck, Deborah Nickerson, et al.
The Journal of Pediatrics|April 17, 2010
Two-tier approach to the newborn screening of methylenetetrahydrofolate reductase deficiency and other remethylation disorders with tandem mass spectrometrySilvia Tortorelli, Coleman T Turgeon, James S Lim, et al.
The Journal of Allergy and Clinical Immunology|July 2, 2013
Newborn screening for severe combined immunodeficiency and T-cell lymphopenia in California: results of the first 2 yearsAntonia Kwan, Joseph A Church, Morton J Cowan, et al.
International Journal of Neonatal Screening|August 18, 2020
A Comparative Effectiveness Study of Newborn Screening Methods for Four Lysosomal Storage DisordersKaren A Sanders, Dimitar K Gavrilov, Devin Oglesbee, et al.
JAMA|August 21, 2014
Newborn screening for severe combined immunodeficiency in 11 screening programs in the United StatesAntonia Kwan, Roshini S Abraham, Robert Currier, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 7, 2012
Enhanced interpretation of newborn screening results without analyte cutoff valuesGregg Marquardt, Robert Currier, David M S McHugh, et al.
Pageof 5