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B A Gordon

Showing results (21-30 of 46) with videos related to

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Pediatric Research|March 1, 1982
Deficiency of the hexosaminidase A activator protein in a case of GM2 gangliosidosis; variant ABP Hechtman, B A Gordon, N M Ng Ying Kin
Pathology, Research and Practice|March 1, 1996
Hyperornithinemia-hyperammonemia-homocitrullinuria (HHH)-syndrome. Ultrastructural changes of mitochondria in cultured dermal fibroblasts of three patientsM D Haust, R A Dewar, D P Gatfield, et al.
Annals of Neurology|July 1, 1982
A variant form of metachromatic leukodystrophy without arylsulfatase deficiencyA F Hahn, B A Gordon, G G Hinton, et al.
The Biochemical Journal|February 1, 1990
Use of a genetic variant to study the hexose transport properties of human skin fibroblastsO T Mesmer, B A Gordon, C A Rupar, et al.
Acta Neuropathologica|January 1, 1981
The AB-variant of metachromatic leukodystrophy (postulated activator protein deficiency). Light and electron microscopic findings in a sural nerve biopsyA F Hahn, B A Gordon, J J Gilbert, et al.
Diabetes, Obesity & Metabolism|January 3, 2013
Insulin sensitivity not modulated 24 to 78 h after acute resistance exercise in type 2 diabetes patientsB A Gordon, S F Fraser, S R Bird, et al.
Diabetes Research and Clinical Practice|January 13, 2009
Resistance training improves metabolic health in type 2 diabetes: a systematic reviewB A Gordon, A C Benson, S R Bird, et al.
Diabetes Research and Clinical Practice|September 28, 2011
Reproducibility of multiple repeated oral glucose tolerance testsB A Gordon, S F Fraser, S R Bird, et al.
Journal of Endocrinological Investigation|October 6, 2011
Insulin sensitivity in response to a single resistance exercise session in apparently healthy individualsB A Gordon, S F Fraser, S R Bird, et al.
The Biochemical Journal|December 15, 1992
Purification and structure of human liver aspartylglucosaminidaseJ W Rip, M B Coulter-Mackie, C A Rupar, et al.
Pageof 5

Showing results (21-30 of 46) with videos related to

Sort By:
Pageof 5
Pediatric Research|March 1, 1982
Deficiency of the hexosaminidase A activator protein in a case of GM2 gangliosidosis; variant ABP Hechtman, B A Gordon, N M Ng Ying Kin
Pathology, Research and Practice|March 1, 1996
Hyperornithinemia-hyperammonemia-homocitrullinuria (HHH)-syndrome. Ultrastructural changes of mitochondria in cultured dermal fibroblasts of three patientsM D Haust, R A Dewar, D P Gatfield, et al.
Annals of Neurology|July 1, 1982
A variant form of metachromatic leukodystrophy without arylsulfatase deficiencyA F Hahn, B A Gordon, G G Hinton, et al.
The Biochemical Journal|February 1, 1990
Use of a genetic variant to study the hexose transport properties of human skin fibroblastsO T Mesmer, B A Gordon, C A Rupar, et al.
Acta Neuropathologica|January 1, 1981
The AB-variant of metachromatic leukodystrophy (postulated activator protein deficiency). Light and electron microscopic findings in a sural nerve biopsyA F Hahn, B A Gordon, J J Gilbert, et al.
Diabetes, Obesity & Metabolism|January 3, 2013
Insulin sensitivity not modulated 24 to 78 h after acute resistance exercise in type 2 diabetes patientsB A Gordon, S F Fraser, S R Bird, et al.
Diabetes Research and Clinical Practice|January 13, 2009
Resistance training improves metabolic health in type 2 diabetes: a systematic reviewB A Gordon, A C Benson, S R Bird, et al.
Diabetes Research and Clinical Practice|September 28, 2011
Reproducibility of multiple repeated oral glucose tolerance testsB A Gordon, S F Fraser, S R Bird, et al.
Journal of Endocrinological Investigation|October 6, 2011
Insulin sensitivity in response to a single resistance exercise session in apparently healthy individualsB A Gordon, S F Fraser, S R Bird, et al.
The Biochemical Journal|December 15, 1992
Purification and structure of human liver aspartylglucosaminidaseJ W Rip, M B Coulter-Mackie, C A Rupar, et al.
Pageof 5