19942019

Research output per year

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Fingerprint Dive into the research topics where Sabrina Prudente is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

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Research Output

A functional variant of the dimethylarginine dimethylaminohydrolase-2 gene is associated with myocardial infarction in type 2 diabetic patients

Mannino, G. C., Pezzilli, S., Averta, C., Fuoco, A., Spiga, R., Mancuso, E., Di Fatta, C., Perticone, F., Prudente, S., Trischitta, V., Andreozzi, F. & Sesti, G., Aug 13 2019, In : Cardiovascular Diabetology. 18, 1, 102.

Research output: Contribution to journalArticle

Open Access
  • Fine-scale haplotype mapping of MUT, AACS, SLC6A15 and PRKCA genes indicates association with insulin resistance of metabolic syndrome and relationship with branched chain amino acid metabolism or regulation

    Haydar, S., Grigorescu, F., Vintilă, M., Cogne, Y., Lautier, C., Tutuncu, Y., Brun, J. F., Robine, J. M., Pugeat, M., Normand, C., Poucheret, P., Gheorghiu, M. L., Georgescu, C., Badiu, C., Băculescu, N., Renard, E., Ylli, D., Badiou, S., Sutra, T., Cristol, J. P. & 20 others, Mercier, J., Gomis, R., Macias, J. M., Litvinov, S., Khusnutdinova, E., Poiana, C., Pasquali, R., Lauro, D., Sesti, G., Prudente, S., Trischitta, V., Tsatsoulis, A., Abdelhak, S., Barakat, A., Zenati, A., Ylli, A., Satman, I., Kanninen, T., Rinato, Y. & Missoni, S., Mar 1 2019, In : PLoS One. 14, 3, e0214122.

    Research output: Contribution to journalArticle

    Open Access
  • Genetic characterization of suspected MODY patients in Tunisia by targeted next-generation sequencing

    Dallali, H., Pezzilli, S., Hechmi, M., Sallem, O. K., Elouej, S., Jmel, H., Ben Halima, Y., Chargui, M., Gharbi, M., Mercuri, L., Alberico, F., Mazza, T., Bahlous, A., Ben Ahmed, M., Jamoussi, H., Abid, A., Trischitta, V., Abdelhak, S., Prudente, S. & Kefi, R., Jan 1 2019, (Accepted/In press) In : Acta Diabetologica.

    Research output: Contribution to journalArticle

  • The novel loss of function Ile354Val mutation in PPARG causes familial partial lipodystrophy

    Padova, G., Prudente, S., Vinciguerra, F., Sudano, D., Baratta, R., Bellacchio, E., Trischitta, V., Vallone, A., Sciacca, L. & Frittitta, L., Dec 20 2019, In : Acta Diabetologica.

    Research output: Contribution to journalArticle

  • The novel loss of function Ile354Val mutation in PPARG causes familial partial lipodystrophy

    Padova, G., Prudente, S., Vinciguerra, F., Sudano, D., Baratta, R., Bellacchio, E., Trischitta, V., Vallone, A., Sciacca, L. & Frittitta, L., Jan 1 2019, (Accepted/In press) In : Acta Diabetologica.

    Research output: Contribution to journalArticle