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Clinical Genetics|March 1, 1985
4-Methylumbelliferyl alpha-N-acetylglucosaminidase activity for diagnosis of Sanfilippo B diseaseJ Marsh, A H FensomClinical Genetics|October 1, 1986
The arylsulphatases of chorionic villi: potential problems in the first-trimester diagnosis of metachromatic leucodystrophy and Maroteaux-Lamy diseaseN Sanguinetti, J Marsh, M Jackson, et al.Clinical Genetics|August 1, 1988
First-trimester diagnosis of metachromatic leucodystrophyA H Fensom, J Marsh, M Jackson, et al.Clinical Genetics|November 1, 1986
Multiple sulphatase deficiency presenting at birthM Burch, A H Fensom, M Jackson, et al.Acta Psychiatrica Scandinavica|July 1, 1990
Leucocyte arylsulphatase A activity and subtypes of chronic schizophreniaA M Heavey, M P Philpot, A H Fensom, et al.Biological Psychiatry|September 1, 1986
Sodium-potassium, magnesium, and calcium ATPase activities in erythrocyte membranes from manic-depressive patients responding to lithiumD R Alexander, M Deeb, F Bitar, et al.Experimental and Clinical Immunogenetics|January 1, 1985
Transplantation of amniotic epithelial membranes in patients with mucopolysaccharidosesC Akle, I McColl, M Dean, et al.Journal of Inherited Metabolic Disease|January 1, 1985
Diagnosis of classical Morquio's disease: N-acetylgalactosamine 6-sulphate sulphatase activity in cultured fibroblasts, leukocytes, amniotic cells and chorionic villiM Yuen, A H FensomClinica Chimica Acta; International Journal of Clinical Chemistry|July 23, 1975
Assay of galactose-1-phosphate uridyl transferase in cultured amniotic cells for prenatal diagnosis of galactosaemiaA H Fensom, P F BensonTransplantation|September 1, 1986
Transplantation of fetal fibroblasts and correction of enzymatic deficiencies in patients with Hunter's or Hurler's disordersM Adinolfi, I McColl, D Chase, et al.Pageof 420