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S Packman

Showing results (11-20 of 98) with videos related to

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Journal of Nutritional Science and Vitaminology|December 1, 1991
Biotin transport in the rat central nervous systemW Lo, T Kadlecek, S Packman
Nature Genetics|July 1, 1997
Deletion of the promoter region in the Atp7a gene of the mottled dappled mouseB Levinson, S Packman, J Gitschier
The Surgical Clinics of North America|June 1, 1995
Indications for parathyroidectomy and extent of treatment for patients with secondary hyperparathyroidismK S Packman, M J Demeure
Human Molecular Genetics|July 1, 1997
Developmental expression of the mouse mottled and toxic milk genes suggests distinct functions for the Menkes and Wilson disease copper transportersY M Kuo, J Gitschier, S Packman
Journal of Inherited Metabolic Disease|November 20, 2009
Psychological aspects of patients with Fabry diseaseT Wilson Crosbie, Wendy Packman, S Packman
Biochemical Genetics|February 1, 1982
Biochemical evidence for diverse etiologies in biotin-responsive multiple carboxylase deficiencyS Packman, N M Caswell, H Baker
Advances in Experimental Medicine and Biology|March 18, 1999
Developmental expression of the mouse mottled and toxic milk genesY M Kuo, J Gitschier, S Packman
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|April 28, 2001
Hyperammonemia in urea cycle disorders: role of the nephrologistR S Mathias, D Kostiner, S Packman
The Journal of Pediatrics|September 1, 1981
The neonatal form of biotin-responsive multiple carboxylase deficiencyS Packman, L Sweetman, H Baker, et al.
American Journal of Medical Genetics|November 1, 1992
Neonatal hemochromatosis: genetic counseling based on retrospective pathologic diagnosisL Ferrell, K Schmidt, V Sheffield, et al.
Pageof 10

Showing results (11-20 of 98) with videos related to

Sort By:
Pageof 10
Journal of Nutritional Science and Vitaminology|December 1, 1991
Biotin transport in the rat central nervous systemW Lo, T Kadlecek, S Packman
Nature Genetics|July 1, 1997
Deletion of the promoter region in the Atp7a gene of the mottled dappled mouseB Levinson, S Packman, J Gitschier
The Surgical Clinics of North America|June 1, 1995
Indications for parathyroidectomy and extent of treatment for patients with secondary hyperparathyroidismK S Packman, M J Demeure
Human Molecular Genetics|July 1, 1997
Developmental expression of the mouse mottled and toxic milk genes suggests distinct functions for the Menkes and Wilson disease copper transportersY M Kuo, J Gitschier, S Packman
Journal of Inherited Metabolic Disease|November 20, 2009
Psychological aspects of patients with Fabry diseaseT Wilson Crosbie, Wendy Packman, S Packman
Biochemical Genetics|February 1, 1982
Biochemical evidence for diverse etiologies in biotin-responsive multiple carboxylase deficiencyS Packman, N M Caswell, H Baker
Advances in Experimental Medicine and Biology|March 18, 1999
Developmental expression of the mouse mottled and toxic milk genesY M Kuo, J Gitschier, S Packman
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|April 28, 2001
Hyperammonemia in urea cycle disorders: role of the nephrologistR S Mathias, D Kostiner, S Packman
The Journal of Pediatrics|September 1, 1981
The neonatal form of biotin-responsive multiple carboxylase deficiencyS Packman, L Sweetman, H Baker, et al.
American Journal of Medical Genetics|November 1, 1992
Neonatal hemochromatosis: genetic counseling based on retrospective pathologic diagnosisL Ferrell, K Schmidt, V Sheffield, et al.
Pageof 10