14 results on '"Fiona Ryan"'
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2. Variability in the diagnosis of growth hormone deficiency using dynamic tests. Time for robust pre-test criteria?
3. The use of urinary steroid profiles in monitoring therapy in children with 21-hydroxylase deficiency - results from the CAH-UK cohort study
4. Management of cranial Diabetes Insipidus in a paediatric tertiary centre - clinical outcomes and patient perception of care
5. Management of cranial Diabetes Insipidus in a tertiary centre - clinical outcomes and patient perception of care
6. Health status of children aged 8-18 years with 21-hydroxylase deficiency in the United Kingdom: results of a multi-centre cohort study
7. Implementation of a novel non-invasive test for monitoring control in individuals with congenital adrenal hyperplasia
8. A case of Idiopathic Infantile Hypercalcaemia (IIH) persisting into adulthood, caused by compound heterozygous mutations of 1,25-dihydroxyvitamin D2 24-hydroxylase (CYP24A1)
9. Uniparental isodisomy as a cause of the autoimmune polyendocrinopathy candidiasis ectodermal dystrophy (APECED) syndrome
10. Rationalising the number of cortisol assays in our low dose synacthen test
11. Idiopathic Infantile Hypercalcaemia (IHH) caused by a missense mutation of 1,25-dihydroxyvitamin D2 24-hydroxylase (CYP24A1)
12. Steroid sick day rules: an audit of caregiver education and confidence levels
13. A case of a rare adrenocortical tumour mimicking neuroblastoma
14. A rare thyrotropinoma complicated by cerebral salt wasting: a case report
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