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J Rhead

Showing results (31-40 of 66) with videos related to

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Journal of Perinatology : Official Journal of the California Perinatal Association|September 1, 1991
A case of glutaric acidemia type II (severe multiple acyl-CoA dehydrogenation disorder) with subsequent prenatal exclusion in a siblingM D Medlock, W J Rhead, L Pollack, et al.
Neurology|February 5, 1999
Short-chain acyl-CoA dehydrogenase deficiency: a cause of ophthalmoplegia and multicore myopathyI Tein, R H Haslam, W J Rhead, 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.
Pediatric Research|January 1, 1989
Short-chain acyl-coenzyme A dehydrogenase deficiency in miceP A Wood, B A Amendt, W 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.
Advances in Experimental Medicine and Biology|March 10, 2000
Lessons learned from the mouse model of short-chain acyl-CoA dehydrogenase deficiencyP A Wood, C L Kelly-Kurtz, M E Hinsdale, et al.
Neurology|December 1, 1991
An atypical case of cytochrome c oxidase deficiency with biochemical heterogeneity in fibroblastsR Lutz, A Garnica, A Shires, 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.
American Journal of Human Genetics|August 1, 1995
Cloning of human very-long-chain acyl-coenzyme A dehydrogenase and molecular characterization of its deficiency in two patientsT Aoyama, M Souri, I Ueno, et al.
Molecular Genetics and Metabolism|March 27, 2002
Evaluation of liver fatty acid oxidation in the leptin-deficient obese mouseAmy E Brix, Ada Elgavish, Tim R Nagy, et al.
Pageof 7

Showing results (31-40 of 66) with videos related to

Sort By:
Pageof 7
Journal of Perinatology : Official Journal of the California Perinatal Association|September 1, 1991
A case of glutaric acidemia type II (severe multiple acyl-CoA dehydrogenation disorder) with subsequent prenatal exclusion in a siblingM D Medlock, W J Rhead, L Pollack, et al.
Neurology|February 5, 1999
Short-chain acyl-CoA dehydrogenase deficiency: a cause of ophthalmoplegia and multicore myopathyI Tein, R H Haslam, W J Rhead, 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.
Pediatric Research|January 1, 1989
Short-chain acyl-coenzyme A dehydrogenase deficiency in miceP A Wood, B A Amendt, W 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.
Advances in Experimental Medicine and Biology|March 10, 2000
Lessons learned from the mouse model of short-chain acyl-CoA dehydrogenase deficiencyP A Wood, C L Kelly-Kurtz, M E Hinsdale, et al.
Neurology|December 1, 1991
An atypical case of cytochrome c oxidase deficiency with biochemical heterogeneity in fibroblastsR Lutz, A Garnica, A Shires, 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.
American Journal of Human Genetics|August 1, 1995
Cloning of human very-long-chain acyl-coenzyme A dehydrogenase and molecular characterization of its deficiency in two patientsT Aoyama, M Souri, I Ueno, et al.
Molecular Genetics and Metabolism|March 27, 2002
Evaluation of liver fatty acid oxidation in the leptin-deficient obese mouseAmy E Brix, Ada Elgavish, Tim R Nagy, et al.
Pageof 7