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Results: 1-5 |
Results: 5

Authors: Kafil-Hussain, NA Monavari, A Bowell, R Thornton, P Naughten, E O'Keefe, M
Citation: Na. Kafil-hussain et al., Ocular findings in glutaric aciduria type 1, J PEDIAT OP, 37(5), 2000, pp. 289-293

Authors: Boers, GHJ Yap, S Naughten, E Wilcken, B
Citation: Ghj. Boers et al., The treatment of high homocysteine concentrations in homocystinuria: Biochemical control in patients and their vascular outcome, DEV CARD M, 230, 2000, pp. 389-411

Authors: Murphy, M McHugh, B Tighe, O Mayne, P O'Neill, C Naughten, E Croke, DT
Citation: M. Murphy et al., Genetic basis of transferase-deficient galactosaemia in Ireland and the population history of the Irish Travellers, EUR J HUM G, 7(5), 1999, pp. 549-554

Authors: Yap, S O'Donnell, KA O'Neill, C Mayne, PD Thornton, P Naughten, E
Citation: S. Yap et al., Factor V Leiden (Arg506Gln), a confounding genetic risk factor but not mandatory for the occurrence of venous thromboembolism in homozygotes and obligate heterozygotes for cystathionine beta-synthase deficiency, THROMB HAEM, 81(4), 1999, pp. 502-505

Authors: Gallagher, PM Naughten, E Hanson, NQ Schwichtenberg, K Bignell, M Yuan, M Ward, P Yap, S Whitehead, AS Tsai, MY
Citation: Pm. Gallagher et al., Characterization of mutations in the cystathionine beta-synthase gene in Irish patients with homocystinuria, MOL GEN MET, 65(4), 1998, pp. 298-302
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