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G T Besley

Showing results (31-40 of 69) with videos related to

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Journal of Inherited Metabolic Disease|January 1, 1991
First trimester diagnosis of inherited metabolic disease: experience in the UKG T Besley, E P Young, A H Fensom, et al.
Acta Neuropathologica|January 1, 1985
Niemann-Pick disease type C. Study on the nature of the cerebral storage processM Elleder, A Jirásek, F Smíd, et al.
European Journal of Pediatrics|October 1, 1989
Phosphorylase b kinase deficiency in a boy with glycogenosis affecting both liver and muscleM Madlom, G T Besley, P T Cohen, et al.
Prenatal Diagnosis|January 1, 1983
Amylo-1,6-glucosidase activity in cultured cells: a deficiency in type III glycogenosis with prenatal studiesG T Besley, P T Cohen, M J Faed, et al.
Journal of Clinical Pathology|November 1, 1979
Sea blue histiocytosis in a patient with chronic non-neuropathic Niemann-Pick diseaseN Dewhurst, G T Besley, N D Finlayson, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Common MCAD mutation in a healthy parent of two affected siblingsL E Heptinstall, J Till, J E Wraith, et al.
Archives of Disease in Childhood|March 1, 1990
Sialic acid storage diseaseP D Cameron, V Dubowitz, G T Besley, et al.
Journal of Clinical Pathology|September 1, 1983
Correlation of lysosomal enzyme abnormalities in various forms of adult leukaemiaG T Besley, S E Moss, A D Bain, et al.
Journal of Clinical Pathology|September 1, 1985
Enzyme markers in acute non-lymphoid leukaemiaG T Besley, S E Moss, A E Dewar, et al.
Postgraduate Medical Journal|October 1, 1987
Adult Gaucher disease in association with acute leukaemiaG M Corbett, P J Darbyshire, G T Besley, et al.
Pageof 7

Showing results (31-40 of 69) with videos related to

Sort By:
Pageof 7
Journal of Inherited Metabolic Disease|January 1, 1991
First trimester diagnosis of inherited metabolic disease: experience in the UKG T Besley, E P Young, A H Fensom, et al.
Acta Neuropathologica|January 1, 1985
Niemann-Pick disease type C. Study on the nature of the cerebral storage processM Elleder, A Jirásek, F Smíd, et al.
European Journal of Pediatrics|October 1, 1989
Phosphorylase b kinase deficiency in a boy with glycogenosis affecting both liver and muscleM Madlom, G T Besley, P T Cohen, et al.
Prenatal Diagnosis|January 1, 1983
Amylo-1,6-glucosidase activity in cultured cells: a deficiency in type III glycogenosis with prenatal studiesG T Besley, P T Cohen, M J Faed, et al.
Journal of Clinical Pathology|November 1, 1979
Sea blue histiocytosis in a patient with chronic non-neuropathic Niemann-Pick diseaseN Dewhurst, G T Besley, N D Finlayson, et al.
Journal of Inherited Metabolic Disease|January 1, 1995
Common MCAD mutation in a healthy parent of two affected siblingsL E Heptinstall, J Till, J E Wraith, et al.
Archives of Disease in Childhood|March 1, 1990
Sialic acid storage diseaseP D Cameron, V Dubowitz, G T Besley, et al.
Journal of Clinical Pathology|September 1, 1983
Correlation of lysosomal enzyme abnormalities in various forms of adult leukaemiaG T Besley, S E Moss, A D Bain, et al.
Journal of Clinical Pathology|September 1, 1985
Enzyme markers in acute non-lymphoid leukaemiaG T Besley, S E Moss, A E Dewar, et al.
Postgraduate Medical Journal|October 1, 1987
Adult Gaucher disease in association with acute leukaemiaG M Corbett, P J Darbyshire, G T Besley, et al.
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