Koulouri, Olympia

Pitfalls in the measurement and interpretation of thyroid function tests

Koulouri, O., Moran, C., Halsall, D., Chatterjee, K., & Gurnell, M. (2013) · Best Practice & Research Clinical Endocrinology & Metabolism

Thyroid Disorders and TreatmentsClinical Laboratory Practices and Quality Control

Cited by 282

Diagnosis and treatment of hypothyroidism in TSH deficiency compared to primary thyroid disease: pituitary patients are at risk of under-replacement with levothyroxine: Diagnosis and treatment of TSH deficiency

Koulouri, O., Auldin, M. A., Agarwal, R., Kieffer, V., Robertson, C., Falconer Smith, J., Levy, M. J., & Howlett, T. A. (2011) · Clinical Endocrinology

Thyroid Disorders and TreatmentsPituitary Gland Disorders and Treatments

Cited by 75

Liver dysfunction in Turner's syndrome: prevalence, natural history and effect of exogenous oestrogen

Koulouri, O., Ostberg, J., & Conway, G. S. (2008) · Clinical Endocrinology

Genetic and Clinical Aspects of Sex Determination and Chromosomal AbnormalitiesSexual Differentiation and Disorders

Cited by 71

A Novel Thyrotropin-Releasing Hormone Receptor Missense Mutation (P81R) in Central Congenital Hypothyroidism

Koulouri, O., Nicholas, A. K., Schoenmakers, E., Mokrosinski, J., Lane, F., Cole, T., Kirk, J., Farooqi, I. S., Chatterjee, V. K., Gurnell, M., et al. (2016) · The Journal of Clinical Endocrinology & Metabolism

Thyroid Disorders and TreatmentsGenomics and Rare Diseases

Cited by 32

A novel IGSF 1 mutation in a large Irish kindred highlights the need for familial screening in the IGSF 1 deficiency syndrome

Roche, E. F., McGowan, A., Koulouri, O., Turgeon, M., Nicholas, A. K., Heffernan, E., El‐Khairi, R., Abid, N., Lyons, G., Halsall, D., et al. (2018) · Clinical Endocrinology

Thyroid Disorders and TreatmentsGenomics and Rare Diseases

Cited by 29