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

par Besley, G T, Bain, A D
Publié 1976

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

par Besley, G T, Broadhead, D M
Publié 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.

par Besley, G T, Snart, R N
Publié 1971

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

par Patrick, W J, Besley, G T, Smith, I I
Publié 1980

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

par Besley, G T, Patrick, A D, Norman, A P
Publié 1969

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

par Judge, M, Moss, S E, Besley, G T, Parker, A C
Publié 1987

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

par Besley, G T, Moss, S E, Bain, A D, Dewar, A E
Publié 1983

Enzyme markers in acute non-lymphoid leukaemia.

par Besley, G T, Moss, S E, Dewar, A E, Eden, O B
Publié 1985

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

par Dewhurst, N, Besley, G T, Finlayson, N D, Parker, A C
Publié 1979

Sialic acid storage disease.

par Cameron, P D, Dubowitz, V, Besley, G T, Fensom, A H
Publié 1990

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

par Sargent, C., Kidd, A., Moore, S., Dean, J., Besley, G., Affara, N.
Publié 2000

Adult Gaucher disease in association with acute leukaemia.

par Corbett, G. M., Darbyshire, P. J., Besley, G. T., Parker, A. C.
Publié 1987

Generalised uridine diphosphate galactose-4-epimerase deficiency

par Walter, J, Roberts, R, Besley, G, Wraith, J, Cleary, M, Holton, J, MacFaul, R
Publié 1999

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

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

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

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

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

par 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
Publié 2008

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

par 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
Publié 1996