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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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Type 2 Diabetes Mellitus Medicine & Life Sciences
Insulin Resistance Medicine & Life Sciences
Insulin Medicine & Life Sciences
Genes Medicine & Life Sciences
Mutation Medicine & Life Sciences
Ataxia Telangiectasia Medicine & Life Sciences
Single Nucleotide Polymorphism Medicine & Life Sciences
Italy Medicine & Life Sciences

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Research Output 1994 2019

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
Myocardial Infarction
Genes
Nitric Oxide
Alleles
Genome-Wide Association Study

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
Branched Chain Amino Acids
branched chain amino acids
amino acid metabolism
metabolic syndrome
Metabolism

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

Tunisia
Mutation
Genes
Inheritance Patterns
Genetic Testing

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

Familial Partial Lipodystrophy
PPAR gamma
Lamin Type A
Mutation
Computer Simulation

Insights from molecular characterization of adult patients of families with multigenerational diabetes

Pezzilli, S., Ludovico, O., Biagini, T., Mercuri, L., Alberico, F., Lauricella, E., Dallali, H., Capocefalo, D., Carella, M., Miccinilli, E., Piscitelli, P., Scarale, M. G., Mazza, T., Trischitta, V. & Prudente, S., Jan 1 2018, In : Diabetes. 67, 1, p. 137-145 9 p.

Research output: Contribution to journalArticle

Genes
Mutation
Pedigree
Research
Hyperglycemia