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