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B Winchester

Showing results (101-110 of 159) with videos related to

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The American Journal of Pathology|December 7, 2000
Reduced heparan sulfate accumulation in enterocytes contributes to protein-losing enteropathy in a congenital disorder of glycosylationV Westphal, S Murch, S Kim, et al.
Biochemical Society Transactions|February 1, 1995
The carbohydrate-deficient glycoprotein syndrome: an experiment of nature in glycosylationB Winchester, P Clayton, N Mian, et al.
Journal of Strength and Conditioning Research|November 17, 2005
Influence of contraction velocity in untrained individuals over the initial early phase of resistance trainingChristopher M Neils, Brian E Udermann, Glenn A Brice, et al.
The Surgical Clinics of North America|October 1, 1991
Laparoscopy and the general surgeonT A Gaskin, J H Isobe, J L Mathews, et al.
Canada Communicable Disease Report = Releve Des Maladies Transmissibles Au Canada|April 3, 1999
Respiratory virus surveillance. FluWatch projectL Pelletier, P Buck, S Herman, et al.
Molecular Genetics and Metabolism|October 10, 2008
Enzyme replacement therapy in Fabry disease: towards a better understanding of the implications of antibody formation and doseC E M Hollak, A C Vedder, B Winchester, et al.
Neuropathology and Applied Neurobiology|April 28, 2006
Autophagic vacuolar myopathy in twin girlsJ L Holton, C Beesley, M Jackson, et al.
Archives of Disease in Childhood|September 1, 1991
Olivopontocerebellar atrophy of neonatal onset and disialotransferrin developmental deficiency syndromeS P Horslen, P T Clayton, B N Harding, et al.
Journal of Inherited Metabolic Disease|August 1, 1997
A novel acid alpha-glucosidase mutation identified in a Pakistani family with glycogen storage disease type IIM A Kroos, A E Waitfield, M Joosse, et al.
Research Quarterly for Exercise and Sport|April 25, 2013
Balance comparisons between female dancers and active nondancersJatin P Ambegaonkar, Shane V Caswell, Jason B Winchester, et al.
Pageof 16

Showing results (101-110 of 159) with videos related to

Sort By:
Pageof 16
The American Journal of Pathology|December 7, 2000
Reduced heparan sulfate accumulation in enterocytes contributes to protein-losing enteropathy in a congenital disorder of glycosylationV Westphal, S Murch, S Kim, et al.
Biochemical Society Transactions|February 1, 1995
The carbohydrate-deficient glycoprotein syndrome: an experiment of nature in glycosylationB Winchester, P Clayton, N Mian, et al.
Journal of Strength and Conditioning Research|November 17, 2005
Influence of contraction velocity in untrained individuals over the initial early phase of resistance trainingChristopher M Neils, Brian E Udermann, Glenn A Brice, et al.
The Surgical Clinics of North America|October 1, 1991
Laparoscopy and the general surgeonT A Gaskin, J H Isobe, J L Mathews, et al.
Canada Communicable Disease Report = Releve Des Maladies Transmissibles Au Canada|April 3, 1999
Respiratory virus surveillance. FluWatch projectL Pelletier, P Buck, S Herman, et al.
Molecular Genetics and Metabolism|October 10, 2008
Enzyme replacement therapy in Fabry disease: towards a better understanding of the implications of antibody formation and doseC E M Hollak, A C Vedder, B Winchester, et al.
Neuropathology and Applied Neurobiology|April 28, 2006
Autophagic vacuolar myopathy in twin girlsJ L Holton, C Beesley, M Jackson, et al.
Archives of Disease in Childhood|September 1, 1991
Olivopontocerebellar atrophy of neonatal onset and disialotransferrin developmental deficiency syndromeS P Horslen, P T Clayton, B N Harding, et al.
Journal of Inherited Metabolic Disease|August 1, 1997
A novel acid alpha-glucosidase mutation identified in a Pakistani family with glycogen storage disease type IIM A Kroos, A E Waitfield, M Joosse, et al.
Research Quarterly for Exercise and Sport|April 25, 2013
Balance comparisons between female dancers and active nondancersJatin P Ambegaonkar, Shane V Caswell, Jason B Winchester, et al.
Pageof 16