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Translation, Validity and Internal Consistency of the Quality of Dying and Death Questionnaire for Brazilian families of patients that died from cancer: a cross-sectional and methodological study.
Paiva BSR, Valentino TCO, Mingardi M, Oliveira MA, Franco JO, Salerno MC, Palocci H, Melo TC, Paiva CE. Paiva BSR, et al. Among authors: salerno mc. Sao Paulo Med J. 2022 Nov 21;141(4):e202285. doi: 10.1590/1516-3180.2022.0085.R2.09082022. eCollection 2022. Sao Paulo Med J. 2022. PMID: 36417658 Free PMC article.
Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients.
Garelli S, Dalla Costa M, Sabbadin C, Barollo S, Rubin B, Scarpa R, Masiero S, Fierabracci A, Bizzarri C, Crinò A, Cappa M, Valenzise M, Meloni A, De Bellis AM, Giordano C, Presotto F, Perniola R, Capalbo D, Salerno MC, Stigliano A, Radetti G, Camozzi V, Greggio NA, Bogazzi F, Chiodini I, Pagotto U, Black SK, Chen S, Rees Smith B, Furmaniak J, Weber G, Pigliaru F, De Sanctis L, Scaroni C, Betterle C. Garelli S, et al. Among authors: salerno mc. J Endocrinol Invest. 2021 Nov;44(11):2493-2510. doi: 10.1007/s40618-021-01585-6. Epub 2021 May 18. J Endocrinol Invest. 2021. PMID: 34003463 Free PMC article.
Familial neurohypophyseal diabetes insipidus in 13 kindreds and 2 novel mutations in the vasopressin gene.
Patti G, Scianguetta S, Roberti D, Di Mascio A, Balsamo A, Brugnara M, Cappa M, Casale M, Cavarzere P, Cipriani S, Corbetta S, Gaudino R, Iughetti L, Martini L, Napoli F, Peri A, Salerno MC, Salerno R, Passeri E, Maghnie M, Perrotta S, Di Iorgi N. Patti G, et al. Among authors: salerno mc. Eur J Endocrinol. 2019 Sep;181(3):233-244. doi: 10.1530/EJE-19-0299. Eur J Endocrinol. 2019. PMID: 31238300 Free article.
Stories of experiences of care for growth hormone deficiency: the CRESCERE project.
Marini MG, Chesi P, Mazzanti L, Guazzarotti L, Toni TD, Salerno MC, Officioso A, Parpagnoli M, Angeletti C, Faienza MF, Iezzi ML, Aversa T, Sacchetti C. Marini MG, et al. Among authors: salerno mc. Future Sci OA. 2016 Feb 25;2(1):FSO82. doi: 10.4155/fso.15.82. eCollection 2016 Mar. Future Sci OA. 2016. PMID: 28031934 Free PMC article.
Multiplex Ligation-Dependent Probe Amplification Accurately Detects Turner Syndrome in Girls with Short Stature.
Grandone A, Del Vecchio Blanco F, Torella A, Caruso M, De Luca F, Di Mase R, Messina MF, Salerno MC, Sallemi A, Perone L, Marzuillo P, Miraglia Del Giudice E, Nigro V, Perrone L. Grandone A, et al. Among authors: salerno mc. Horm Res Paediatr. 2016;86(5):330-336. doi: 10.1159/000452219. Epub 2016 Oct 27. Horm Res Paediatr. 2016. PMID: 27784012 Clinical Trial.
Frequency of genetic defects in combined pituitary hormone deficiency: a systematic review and analysis of a multicentre Italian cohort.
De Rienzo F, Mellone S, Bellone S, Babu D, Fusco I, Prodam F, Petri A, Muniswamy R, De Luca F, Salerno M, Momigliano-Richardi P, Bona G, Giordano M; Italian Study Group on Genetics of CPHD. De Rienzo F, et al. Clin Endocrinol (Oxf). 2015 Dec;83(6):849-60. doi: 10.1111/cen.12849. Epub 2015 Aug 6. Clin Endocrinol (Oxf). 2015. PMID: 26147833 Review.
Early-onset central diabetes insipidus is associated with de novo arginine vasopressin-neurophysin II or Wolfram syndrome 1 gene mutations.
Perrotta S, Di Iorgi N, Ragione FD, Scianguetta S, Borriello A, Allegri AE, Ferraro M, Santoro C, Napoli F, Calcagno A, Giaccardi M, Cappa M, Salerno MC, Cozzolino D, Maghnie M. Perrotta S, et al. Among authors: salerno mc. Eur J Endocrinol. 2015 Apr;172(4):461-72. doi: 10.1530/EJE-14-0942. Eur J Endocrinol. 2015. PMID: 25740874
28 results