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D Steiner

Showing results (181-190 of 356) with videos related to

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Clinica Chimica Acta; International Journal of Clinical Chemistry|October 8, 2009
ESI-MS/MS quantification of 7alpha-hydroxy-4-cholesten-3-one facilitates rapid, convenient diagnostic testing for cerebrotendinous xanthomatosisAndrea E DeBarber, William E Connor, Anuradha S Pappu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 16, 2004
Iron status of children with phenylketonuria undergoing nutrition therapy assessed by transferrin receptorsPhyllis B Acosta, Steven Yannicelli, Rani H Singh, et al.
Journal of Obstetric, Gynecologic, and Neonatal Nursing : JOGNN|September 25, 2015
Commitment to Breastfeeding in the Context of PhenylketonuriaSandra A Banta-Wright, Sheila M Kodadek, Gail M Houck, et al.
Journal of Inherited Metabolic Disease|July 24, 2008
Correlates of language impairment in children with galactosaemiaN L Potter, J-A C Lazarus, J M Johnson, et al.
Annals of Family Medicine|July 16, 2008
Community care of North Carolina: improving care through community health networksBeat D Steiner, Amy C Denham, Evan Ashkin, et al.
American Journal of Public Health|July 23, 2011
Using geographic information systems to match local health needs with public health services and programsTamara Dubowitz, Malcolm Williams, Elizabeth D Steiner, et al.
Molecular Genetics and Metabolism|June 8, 2002
Cholesterol storage defect in RSH/Smith-Lemli-Opitz syndrome fibroblastsChristopher A Wassif, Donna Vied, Maria Tsokos, et al.
Molecular Genetics and Metabolism|October 7, 2004
Lowered DHCR7 activity measured by ergosterol conversion in multiple cell types in Smith-Lemli-Opitz syndromeSharon Ginat, Kevin P Battaile, Brian C Battaile, et al.
Molecular Genetics and Metabolism Reports|June 23, 2016
Update on newborn dried bloodspot testing for cerebrotendinous xanthomatosis: An available high-throughput liquid-chromatography tandem mass spectrometry methodLisa Bleyle, Hidde H Huidekoper, Frederic M Vaz, et al.
Pediatrics|July 4, 2007
Screening and treatment for lipid disorders in children and adolescents: systematic evidence review for the US Preventive Services Task ForceElizabeth M Haney, Laurie Hoyt Huffman, Christina Bougatsos, et al.
Pageof 36

Showing results (181-190 of 356) with videos related to

Sort By:
Pageof 36
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 8, 2009
ESI-MS/MS quantification of 7alpha-hydroxy-4-cholesten-3-one facilitates rapid, convenient diagnostic testing for cerebrotendinous xanthomatosisAndrea E DeBarber, William E Connor, Anuradha S Pappu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 16, 2004
Iron status of children with phenylketonuria undergoing nutrition therapy assessed by transferrin receptorsPhyllis B Acosta, Steven Yannicelli, Rani H Singh, et al.
Journal of Obstetric, Gynecologic, and Neonatal Nursing : JOGNN|September 25, 2015
Commitment to Breastfeeding in the Context of PhenylketonuriaSandra A Banta-Wright, Sheila M Kodadek, Gail M Houck, et al.
Journal of Inherited Metabolic Disease|July 24, 2008
Correlates of language impairment in children with galactosaemiaN L Potter, J-A C Lazarus, J M Johnson, et al.
Annals of Family Medicine|July 16, 2008
Community care of North Carolina: improving care through community health networksBeat D Steiner, Amy C Denham, Evan Ashkin, et al.
American Journal of Public Health|July 23, 2011
Using geographic information systems to match local health needs with public health services and programsTamara Dubowitz, Malcolm Williams, Elizabeth D Steiner, et al.
Molecular Genetics and Metabolism|June 8, 2002
Cholesterol storage defect in RSH/Smith-Lemli-Opitz syndrome fibroblastsChristopher A Wassif, Donna Vied, Maria Tsokos, et al.
Molecular Genetics and Metabolism|October 7, 2004
Lowered DHCR7 activity measured by ergosterol conversion in multiple cell types in Smith-Lemli-Opitz syndromeSharon Ginat, Kevin P Battaile, Brian C Battaile, et al.
Molecular Genetics and Metabolism Reports|June 23, 2016
Update on newborn dried bloodspot testing for cerebrotendinous xanthomatosis: An available high-throughput liquid-chromatography tandem mass spectrometry methodLisa Bleyle, Hidde H Huidekoper, Frederic M Vaz, et al.
Pediatrics|July 4, 2007
Screening and treatment for lipid disorders in children and adolescents: systematic evidence review for the US Preventive Services Task ForceElizabeth M Haney, Laurie Hoyt Huffman, Christina Bougatsos, et al.
Pageof 36