Search research articles
Contact Us
Filters
Showing results (21-30 of 46) with videos related to
Page
of 5
Sort By:
Pediatric Research
|
March 1, 1982
Deficiency of the hexosaminidase A activator protein in a case of GM2 gangliosidosis; variant AB
P 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 patients
M D Haust, R A Dewar, D P Gatfield, et al.
Annals of Neurology
|
July 1, 1982
A variant form of metachromatic leukodystrophy without arylsulfatase deficiency
A 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 fibroblasts
O 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 biopsy
A 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 patients
B 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 review
B 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 tests
B 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 individuals
B A Gordon, S F Fraser, S R Bird, et al.
The Biochemical Journal
|
December 15, 1992
Purification and structure of human liver aspartylglucosaminidase
J W Rip, M B Coulter-Mackie, C A Rupar, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 46) with videos related to
Sort By:
Page
of 5
Pediatric Research
|
March 1, 1982
Deficiency of the hexosaminidase A activator protein in a case of GM2 gangliosidosis; variant AB
P 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 patients
M D Haust, R A Dewar, D P Gatfield, et al.
Annals of Neurology
|
July 1, 1982
A variant form of metachromatic leukodystrophy without arylsulfatase deficiency
A 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 fibroblasts
O 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 biopsy
A 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 patients
B 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 review
B 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 tests
B 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 individuals
B A Gordon, S F Fraser, S R Bird, et al.
The Biochemical Journal
|
December 15, 1992
Purification and structure of human liver aspartylglucosaminidase
J W Rip, M B Coulter-Mackie, C A Rupar, et al.
Page
of 5