Pubblicazioni

Polygenic inheritance of cryptorchidism susceptibility in the LE/orl rat

2016 - MOLECULAR HUMAN REPRODUCTION

Barthold, Julia Spencer; Pugarelli, Joan; Macdonald, Madolyn L.; Ren, Jia; Adetunji, Modupeore O.; Polson, Shawn W.; Mateson, Abigail; Wang, Yanping; Sol Church, Katia; Mccahan, Suzanne M.; Akins, Robert E.; Devoto, Marcella; Erobbins, Alan K.

Congenital immunodeficiency in an individual with WiedemannÃ¢ÂÂSteiner syndrome due to a novel missense mutation in KMT2A

2016 - AMERICAN JOURNAL OF MEDICAL GENETICS. PART A

Stellacci, Emilia; Onesimo, Roberta; Bruselles, Alessandro; Pizzi, Simone; Battaglia, Domenica; Leoni, Chiara; Zampino, Giuseppe; Tartaglia, Marco

The PPARÎ³2 P12A polymorphism is not associated with all-cause mortality in patients with type 2 diabetes mellitus

2016 - ENDOCRINE

Pacilli, Antonio; Prudente, Sabrina; Copetti, Massimiliano; Fontana, Andrea; Mercuri, Luana; Bacci, Simonetta; Marucci, Antonella; Alberico, Federica; Viti, Raffaella; Palena, Antonio; Lamacchia, Olga; Cignarelli, Mauro; De Cosmo, Salvatore; Trischitta, Vincenzo

GALNT2 mRNA levels are associated with serum triglycerides in humans

2016 - ENDOCRINE

Marucci, Antonella; Mangiacotti, Davide; Trischitta, Vincenzo; Di Paola, Rosa

Evidence of a causal relationship between high serum adiponectin levels and increased cardiovascular mortality rate in patients with type 2 diabetes

2016 - CARDIOVASCULAR DIABETOLOGY

Ortega Moreno, Lorena; Copetti, Massimiliano; Fontana, Andrea; Bonis, Concetta; Salvemini, Lucia; Trischitta, Vincenzo; Menzaghi, Claudia

Characterization of endocrine features and genotype-phenotypes correlations in blepharophimosis-ptosis-epicanthus inversus syndrome type 1

2016 - JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION

Nuovo, S.; Passeri, M.; Di Benedetto, E.; Calanchini, M.; Meldolesi, I.; Di Giacomo, M. C.; Petruzzi, D.; Piemontese, M. R.; Zelante, L.; Sangiuolo, F.; Novelli, G.; Fabbri, A.; Brancati, F.