Cordeddu, Viviana

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

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Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: Molecular diversity and associated phenotypic spectrum

Sarkozy, A., Carta, C., Moretti, S., Zampino, G., Digilio, M. C., Pantaleoni, F., Scioletti, A. P., Esposito, G., Cordeddu, V., Lepri, F., et al. (2009) · Human Mutation

Protein Tyrosine PhosphatasesGenomics and Rare Diseases

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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

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Gene Therapy in Retinal Dystrophies

Ziccardi, L., Cordeddu, V., Gaddini, L., Matteucci, A., Parravano, M., Malchiodi-Albedi, F., & Varano, M. (2019) · International Journal of Molecular Sciences

Retinal Development and DisordersVirus-based gene therapy research

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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

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