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QJM : Monthly Journal of the Association of Physicians|February 20, 1999
Hereditary juvenile haemochromatosis: a genetically heterogeneous life-threatening iron-storage diseaseA L Kelly, D A Rhodes, J M Roland, et al.The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society|January 20, 2000
Osteoclastic tartrate-resistant acid phosphatase (Acp 5): its localization to dendritic cells and diverse murine tissuesA R Hayman, A J Bune, J R Bradley, et al.QJM : Monthly Journal of the Association of Physicians|January 1, 1997
Pro-inflammatory cytokines and the pathogenesis of Gaucher's disease: increased release of interleukin-6 and interleukin-10M J Allen, B J Myer, A M Khokher, et al.Journal of Neurochemistry|January 1, 1997
The tau protein in human cerebrospinal fluid in Alzheimer's disease consists of proteolytically derived fragmentsG V Johnson, P Seubert, T M Cox, et al.JPEN. Journal of Parenteral and Enteral Nutrition|January 1, 1997
Skeletal muscle weakness and dysphagia caused by acid maltase deficiency: nutritional consequences of coincident celiac sprueT S King, J R Anderson, E P Wraight, et al.Human Genetics|October 1, 1990
Molecular analysis of the human MHC class I region in hereditary haemochromatosis. A study by pulsed-field gel electrophoresisD K Lord, I Dunham, R D Campbell, et al.Gut|July 1, 1979
Rôle of calcitonin in diarrhoea associated with medullary carcinoma of the thyroidT M Cox, E A Fagan, C J Hillyard, et al.Journal of Medical Genetics|June 1, 1994
Null alleles of the aldolase B gene in patients with hereditary fructose intoleranceM Ali, G Tunçman, N C Cross, et al.Infection and Immunity|April 1, 1993
Schistosoma japonicum-infected mice show reduced hepatic fibrosis and eosinophilia and selective inhibition of interleukin-5 secretion by CD4+ cells after treatment with anti-interleukin-2 antibodiesA W Cheever, Y Xu, A Sher, et al.Lancet (London, England)|April 11, 1992
Genetic diagnosis of Gaucher's diseaseP K Mistry, S J Smith, M Ali, et al.Pageof 12