Braccesi G - Search Results

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Clinical and molecular characterization of a novel INS mutation identified in patients with MODY phenotype.

Piccini B, Artuso R, Lenzi L, Guasti M, Braccesi G, Barni F, Casalini E, Giglio S, Toni S. Piccini B, et al. Among authors: braccesi g. Eur J Med Genet. 2016 Nov;59(11):590-595. doi: 10.1016/j.ejmg.2016.09.016. Epub 2016 Sep 19. Eur J Med Genet. 2016. PMID: 27659712

Continuous subcutaneous infusion of protein C concentrate using an insulin pump in a newborn with congenital protein C deficiency.

Piccini B, Capirchio L, Lenzi L, Guasti M, Braccesi G, Bresci C, Casalini E, Fiorini P, Agostini E, Toni S. Piccini B, et al. Among authors: braccesi g. Blood Coagul Fibrinolysis. 2014 Jul;25(5):522-6. doi: 10.1097/MBC.0000000000000079. Blood Coagul Fibrinolysis. 2014. PMID: 24509341

Sydenham's chorea in a girl with juvenile idiopathic arthritis treated with anti-TNFalpha therapy.

Cimaz R, Gana S, Braccesi G, Guerrini R. Cimaz R, et al. Among authors: braccesi g. Mov Disord. 2010 Mar 15;25(4):511-4. doi: 10.1002/mds.22923. Mov Disord. 2010. PMID: 20014056 No abstract available.

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