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Journal of Inherited Metabolic Disease|June 19, 2001
Amino acids: analytical aspectsP D Mayne, G Roche, D DeverellThrombosis and Haemostasis|May 11, 1999
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 deficiencyS Yap, K A O'Donnell, C O'Neill, et al.Human Mutation|April 24, 2001
Rapid detection of the R408W and I65T mutations in phenylketonuria by glycosylase mediated polymorphism detectionK A O'Donnell, O Tighe, C O'Neill, et al.Journal of Inherited Metabolic Disease|November 20, 1998
Homocystinuria due to cystathionine beta-synthase deficiency in Ireland: 25 years' experience of a newborn screened and treated population with reference to clinical outcome and biochemical controlS Yap, E NaughtenJournal of Inherited Metabolic Disease|January 1, 1990
Maternal phenylketonuria--the Irish experienceE Naughten, I P SaulLancet (London, England)|October 8, 1977
Vitamin D and human lactationA Fairney, E Naughten, T E OppéAnnals of Clinical Biochemistry|March 1, 1991
Calcium and phosphorus metabolism in the premature infantP D Mayne, I Z KovarIrish Medical Journal|December 6, 2006
Mitochondrial cytopathies, phenotypic heterogeneity and a high incidenceE Ryan, M D King, P Rustin, et al.American Journal of Diseases of Children (1960)|August 1, 1982
At what age do diabetic children give their own injections?E Naughten, M A Smith, J D BaumPageof 225