Campi, Irene

Mutations in the selenocysteine insertion sequence-binding protein 2 gene lead to a multisystem selenoprotein deficiency disorder in humans

Schoenmakers, E., Agostini, M., Mitchell, C., Schoenmakers, N., Papp, L., Rajanayagam, O., Padidela, R., Ceron-Gutierrez, L., Doffinger, R., Prevosto, C., et al. (2010) · Journal of Clinical Investigation

Selenium in Biological SystemsOrganoselenium and organotellurium chemistry

Cited by 315

Loss-of-function mutations in IGSF1 cause an X-linked syndrome of central hypothyroidism and testicular enlargement

Sun, Y., Bak, B., Schoenmakers, N., van Trotsenburg, A. S. P., Oostdijk, W., Voshol, P., Cambridge, E., White, J. K., le Tissier, P., Gharavy, S. N. M., et al. (2012) · Nature Genetics

Thyroid Disorders and TreatmentsHypothalamic control of reproductive hormones

Cited by 217

Graves’ Orbitopathy Activation after Radioactive Iodine Therapy with and without Steroid Prophylaxis

Vannucchi, G., Campi, I., Covelli, D., Dazzi, D., Currò, N., Simonetta, S., Ratiglia, R., Beck-Peccoz, P., & Salvi, M. (2009) · The Journal of Clinical Endocrinology & Metabolism

Ophthalmology and Eye DisordersMyasthenia Gravis and Thymoma

Cited by 92

Thyrotropin-Secreting Pituitary Adenomas: Outcome of Pituitary Surgery and Irradiation

Malchiodi, E., Profka, E., Ferrante, E., Sala, E., Verrua, E., Campi, I., Lania, A. G., Arosio, M., Locatelli, M., Mortini, P., et al. (2014) · The Journal of Clinical Endocrinology & Metabolism

Pituitary Gland Disorders and TreatmentsNeuroendocrine Tumor Research Advances

Cited by 89

Unusual causes of hyperthyrotropinemia and differential diagnosis of primary hypothyroidism: a revised diagnostic flowchart

Campi, I., Dell’Acqua, M., Stellaria Grassi, E., Cristina Vigone, M., & Persani, L. (2023) · European Thyroid Journal

Thyroid Disorders and TreatmentsThyroid and Parathyroid Surgery

Cited by 13