Sorcini, Mariella

Diversity and functional consequences of germline and somatic PTPN11 mutations in human disease

Tartaglia, M., Martinelli, S., Stella, L., Bocchinfuso, G., Flex, E., Cordeddu, V., Zampino, G., van der Burgt, I., Palleschi, A., Petrucci, T. C., et al. (2006) · The American Journal of Human Genetics

Protein Tyrosine PhosphatasesProtein Kinase Regulation and GTPase Signaling

Cited by 415

A Population-Based Study on the Frequency of Additional Congenital Malformations in Infants with Congenital Hypothyroidism: Data from the Italian Registry for Congenital Hypothyroidism (1991–1998)

Olivieri, A., Stazi, M. A., Mastroiacovo, P., Fazzini, C., Medda, E., Spagnolo, A., De Angelis, S., Grandolfo, M. E., Taruscio, D., Cordeddu, V., et al. (2002) · The Journal of Clinical Endocrinology & Metabolism

Thyroid Disorders and TreatmentsCongenital limb and hand anomalies

Cited by 224

Role of galectin-3 in diabetic nephropathy

Iacobini, C., Amadio, L., Oddi, G., Ricci, C., Barsotti, P., Missori, S., Sorcini, M., Di Mario, U., Pricci, F., & Pugliese, G. (2003) · Journal of the American Society of Nephrology

Advanced Glycation End Products researchGalectins and Cancer Biology

Cited by 99

High Risk of Congenital Hypothyroidism in Multiple Pregnancies

Olivieri, A., Medda, E., De Angelis, S., Valensise, H., De Felice, M., Fazzini, C., Cascino, I., Cordeddu, V., Sorcini, M., & Stazi, M. A. (2007) · The Journal of Clinical Endocrinology & Metabolism

Thyroid Disorders and TreatmentsAssisted Reproductive Technology and Twin Pregnancy

Cited by 70