Krabbe's globoid cell leucodystrophy. Studies on galactosylceramide beta-galactosidase and non-specific beta-galactosidase of leucocytes, cultured skin fibroblasts, and amniotic fl...

por Besley, G T, Bain, A D
Publicado 1976

Studies on human N-acetyl-Beta-d-hexosaminidase C separated from neonatal brain.

por Besley, G T, Broadhead, D M
Publicado 1976

Effect of vasopressin on the uptake of calcium ions by kidney mitochondria and on the concentration of adenosine 3':5'-cyclic monophosphate in toad bladder.

por Besley, G T, Snart, R N
Publicado 1971

Histochemical diagnosis of Hirschsprung's disease and a comparison of the histochemical and biochemical activity of acetylcholinesterase in rectal mucosal biopsies.

por Patrick, W J, Besley, G T, Smith, I I
Publicado 1980

Inhibition of the motility of gill cilia of Dreissensia by plasma of cystic fibrosis patients and their parents.

por Besley, G T, Patrick, A D, Norman, A P
Publicado 1969

Lysosomal enzyme abnormalities in preleukaemic Sweet's disease: case report.

por Judge, M, Moss, S E, Besley, G T, Parker, A C
Publicado 1987

Correlation of lysosomal enzyme abnormalities in various forms of adult leukaemia.

por Besley, G T, Moss, S E, Bain, A D, Dewar, A E
Publicado 1983

Enzyme markers in acute non-lymphoid leukaemia.

por Besley, G T, Moss, S E, Dewar, A E, Eden, O B
Publicado 1985

Sea blue histiocytosis in a patient with chronic non-neuropathic Niemann-Pick disease.

por Dewhurst, N, Besley, G T, Finlayson, N D, Parker, A C
Publicado 1979

Sialic acid storage disease.

por Cameron, P D, Dubowitz, V, Besley, G T, Fensom, A H
Publicado 1990

Five cases of isolated glycerol kinase deficiency, including two families: failure to find genotype:phenotype correlation

por Sargent, C., Kidd, A., Moore, S., Dean, J., Besley, G., Affara, N.
Publicado 2000

Adult Gaucher disease in association with acute leukaemia.

por Corbett, G. M., Darbyshire, P. J., Besley, G. T., Parker, A. C.
Publicado 1987

Generalised uridine diphosphate galactose-4-epimerase deficiency

por Walter, J, Roberts, R, Besley, G, Wraith, J, Cleary, M, Holton, J, MacFaul, R
Publicado 1999

Acid maltase deficiency presenting with a myopathy and exercise induced urinary incontinence in a 68 year old male.

por Chancellor, A M, Warlow, C P, Webb, J N, Lucas, M G, Besley, G T, Broadhead, D M
Publicado 1991

Defective PEX gene products correlate with the protein import, biochemical abnormalities, and phenotypic heterogeneity in peroxisome biogenesis disorders

por Shimozawa, N., Imamura, A., Zhang, Z., Suzuki, Y., Orii, T., Tsukamoto, T., Osumi, T., Fujiki, Y., Wanders, R., Besley, G., Kondo, N.
Publicado 1999

Skewed X inactivation is associated with phenotype in a female with adrenal hypoplasia congenita

por Shaikh, M G, Boyes, L, Kingston, H, Collins, R, Besley, G T N, Padmakumar, B, Ismayl, O, Hughes, I, Hall, C M, Hellerud, C, Achermann, J C, Clayton, P E
Publicado 2008

Long-term in vitro correction of alpha-L-iduronidase deficiency (Hurler syndrome) in human bone marrow.

por Fairbairn, L J, Lashford, L S, Spooncer, E, McDermott, R H, Lebens, G, Arrand, J E, Arrand, J R, Bellantuono, I, Holt, R, Hatton, C E, Cooper, A, Besley, G T, Wraith, J E, Anson, D S, Hopwood, J J, Dexter, T M
Publicado 1996