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A new mutation in the CAVIN1/PTRF gene in two siblings with congenital generalized lipodystrophy type 4: case reports and review of the literature.
Mancioppi V, Daffara T, Romanisio M, Ceccarini G, Pelosini C, Santini F, Bellone S, Mellone S, Baricich A, Rabbone I, Aimaretti G, Akinci B, Giordano M, Prodam F. Mancioppi V, et al. Among authors: ceccarini g. Front Endocrinol (Lausanne). 2023 Jul 12;14:1212729. doi: 10.3389/fendo.2023.1212729. eCollection 2023. Front Endocrinol (Lausanne). 2023. PMID: 37501786 Free PMC article. Review.
Role for inner ring deiodination preventing transcutaneous passage of thyroxine.
Santini F, Vitti P, Chiovato L, Ceccarini G, Macchia M, Montanelli L, Gatti G, Rosellini V, Mammoli C, Martino E, Chopra IJ, Safer JD, Braverman LE, Pinchera A. Santini F, et al. Among authors: ceccarini g. J Clin Endocrinol Metab. 2003 Jun;88(6):2825-30. doi: 10.1210/jc.2002-021439. J Clin Endocrinol Metab. 2003. PMID: 12788895
Genetic screening for melanocortin-4 receptor mutations in a cohort of Italian obese patients: description and functional characterization of a novel mutation.
Santini F, Maffei M, Ceccarini G, Pelosini C, Scartabelli G, Rosellini V, Chiellini C, Marsili A, Lisi S, Tonacchera M, Agretti P, Chiovato L, Mammoli C, Vitti P, Pinchera A. Santini F, et al. Among authors: ceccarini g. J Clin Endocrinol Metab. 2004 Feb;89(2):904-8. doi: 10.1210/jc.2003-031175. J Clin Endocrinol Metab. 2004. PMID: 14764812
Serum insulin-like growth factor-1 concentrations are reduced in severely obese women and raise after weight loss induced by laparoscopic adjustable gastric banding.
Galli G, Pinchera A, Piaggi P, Fierabracci P, Giannetti M, Querci G, Scartabelli G, Manetti L, Ceccarini G, Martinelli S, Di Salvo C, Anselmino M, Bogazzi F, Landi A, Vitti P, Maffei M, Santini F. Galli G, et al. Among authors: ceccarini g. Obes Surg. 2012 Aug;22(8):1276-80. doi: 10.1007/s11695-012-0669-1. Obes Surg. 2012. PMID: 22648796
Frequency of the GPR7 Tyr135Phe allelic variant in lean and obese subjects.
Pelosini C, Maffei M, Ceccarini G, Marchi M, Marsili A, Galli G, Scartabelli G, Tamberi A, Latrofa F, Fierabracci P, Vitti P, Pinchera A, Santini F. Pelosini C, et al. Among authors: ceccarini g. J Endocrinol Invest. 2013 Oct;36(9):712-5. doi: 10.3275/8929. Epub 2013 Apr 8. J Endocrinol Invest. 2013. PMID: 23563248
Identification of a novel mutation in the polymerase delta 1 (POLD1) gene in a lipodystrophic patient affected by mandibular hypoplasia, deafness, progeroid features (MDPL) syndrome.
Pelosini C, Martinelli S, Ceccarini G, Magno S, Barone I, Basolo A, Fierabracci P, Vitti P, Maffei M, Santini F. Pelosini C, et al. Among authors: ceccarini g. Metabolism. 2014 Nov;63(11):1385-9. doi: 10.1016/j.metabol.2014.07.010. Epub 2014 Jul 25. Metabolism. 2014. PMID: 25131834
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