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William J Rhead

Showing results (1-10 of 18) with videos related to

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Journal of Inherited Metabolic Disease|June 10, 2006
Newborn screening for medium-chain acyl-CoA dehydrogenase deficiency: a global perspectiveWilliam J Rhead
Pediatric Clinics of North America|May 26, 2004
The call from the newborn screening laboratory: frustration in the afternoonWilliam J Rhead, Mira Irons
Methods in Molecular Biology (Clifton, N.J.)|January 16, 2010
Identification of urine organic acids for the detection of inborn errors of metabolism using urease and gas chromatography-mass spectrometry (GC-MS)Stanley F Lo, Velta Young, William J Rhead
Methods in Molecular Biology (Clifton, N.J.)|September 20, 2022
Identification of Urine Organic Acids for the Detection of Inborn Errors of Metabolism Using Urease and Gas Chromatography-Mass Spectrometry (GC/MS)Stanley F Lo, Keely Pierzchalski, Velta Young, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 22, 2008
Creating genetics-based infusion centers: a case study of two modelsDawn J Laney, Amy L White, William J Rhead, et al.
American Journal of Medical Genetics. Part A|September 2, 2003
Genitopatellar syndrome: expanding the phenotypeCaroline A Lifchez, William J Rhead, Steven R Leuthner, et al.
Critical Care Clinics|October 18, 2005
Nutritional management of urea cycle disordersRani H Singh, William J Rhead, Wendy Smith, et al.
Critical Care Clinics|October 18, 2005
Considerations in the difficult-to-manage urea cycle disorder patientBrendan Lee, Rani H Singh, William J Rhead, et al.
Critical Care Clinics|October 18, 2005
Genetic counseling issues in urea cycle disordersLisa Sniderman King, Rani H Singh, William J Rhead, et al.
Molecular Genetics and Metabolism|November 21, 2007
Rescue from neonatal death in the murine model of hereditary tyrosinemia by glutathione monoethylester and vitamin C treatmentChantale Langlois, Rossana Jorquera, Diana Orejuela, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
Journal of Inherited Metabolic Disease|June 10, 2006
Newborn screening for medium-chain acyl-CoA dehydrogenase deficiency: a global perspectiveWilliam J Rhead
Pediatric Clinics of North America|May 26, 2004
The call from the newborn screening laboratory: frustration in the afternoonWilliam J Rhead, Mira Irons
Methods in Molecular Biology (Clifton, N.J.)|January 16, 2010
Identification of urine organic acids for the detection of inborn errors of metabolism using urease and gas chromatography-mass spectrometry (GC-MS)Stanley F Lo, Velta Young, William J Rhead
Methods in Molecular Biology (Clifton, N.J.)|September 20, 2022
Identification of Urine Organic Acids for the Detection of Inborn Errors of Metabolism Using Urease and Gas Chromatography-Mass Spectrometry (GC/MS)Stanley F Lo, Keely Pierzchalski, Velta Young, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 22, 2008
Creating genetics-based infusion centers: a case study of two modelsDawn J Laney, Amy L White, William J Rhead, et al.
American Journal of Medical Genetics. Part A|September 2, 2003
Genitopatellar syndrome: expanding the phenotypeCaroline A Lifchez, William J Rhead, Steven R Leuthner, et al.
Critical Care Clinics|October 18, 2005
Nutritional management of urea cycle disordersRani H Singh, William J Rhead, Wendy Smith, et al.
Critical Care Clinics|October 18, 2005
Considerations in the difficult-to-manage urea cycle disorder patientBrendan Lee, Rani H Singh, William J Rhead, et al.
Critical Care Clinics|October 18, 2005
Genetic counseling issues in urea cycle disordersLisa Sniderman King, Rani H Singh, William J Rhead, et al.
Molecular Genetics and Metabolism|November 21, 2007
Rescue from neonatal death in the murine model of hereditary tyrosinemia by glutathione monoethylester and vitamin C treatmentChantale Langlois, Rossana Jorquera, Diana Orejuela, et al.
Pageof 2