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Pelagatti MA, Meini A, Caorsi R, Cattalini M, Federici S, Zulian F, Calcagno G, Tommasini A, Bossi G, Sormani MP, Caroli F, Plebani A, Ceccherini I, Martini A, Gattorno M. Long-term clinical profile of children with the low-penetrance R92Q mutation of the TNFRSF1A gene. Arthritis Rheum 2011;63(4):1141-50.
Pederiva F, Paloni G, Berti I. Subcutaneous Granuloma Annulare: A Diagnostic Conundrum-Learning From Mistakes. Pediatr Emerg Care 2017;33(8):e30-e31.
Pederiva F, Guida E, Codrich D, Scarpa MG, Olenik D, Schleef J. Laparoscopic orchiopexy: short term outcomes. Experience of a single centre. Minerva Pediatr 2015;
Pederiva F, Guida E, Maschio M, Rigamonti W, Gregori M, Codrich D. Handlebar injury in children: The hidden danger. Surgery 2015;
Pederiva F, Daniela C, Scarpa M-G, Guida E, Dragovic D, Martelossi S. An asymptomatic multiple magnet ingestion with transmesenteric entero-enteric fistula. APSP J Case Rep 2014;5(2):16.
Pederiva F, Barbi E, Zennaro F, Neri E. Fainting Starting Parenteral Nutrition. Pediatr Emerg Care 2015;31(9):648.
Pecci A, Ma X, Savoia A, Adelstein RS. MYH9: Structure, functions and role of non-muscle myosin IIA in human disease. Gene 2018;664:152-167.
Pecci A, Klersy C, Gresele P, Lee KJD, De Rocco D, Bozzi V, Russo G, Heller PG, Loffredo G, Ballmaier M, Fabris F, Beggiato E, Kahr WHA, Pujol-Moix N, Platokouki H, Van Geet C, Noris P, Yerram P, Hermans C, Gerber B, Economou M, De Groot M, Zieger B, De Candia E, Fraticelli V, Kersseboom R, Piccoli GB, Zimmermann S, Fierro T, Glembotsky AC, Vianello F, Zaninetti C, Nicchia E, Güthner C, Baronci C, Seri M, Knight PJ, Balduini CL, Savoia A. MYH9-related disease: a novel prognostic model to predict the clinical evolution of the disease based on genotype-phenotype correlations. Hum Mutat 2014;35(2):236-47.
Pecci A, Biino G, Fierro T, Bozzi V, Mezzasoma A, Noris P, Ramenghi U, Loffredo G, Fabris F, Momi S, Magrini U, Pirastu M, Savoia A, Balduini C, Gresele P. Alteration of liver enzymes is a feature of the MYH9-related disease syndrome. PLoS One 2012;7(4):e35986.
Pecci A, Gresele P, Klersy C, Savoia A, Noris P, Fierro T, Bozzi V, Mezzasoma AMaria, Melazzini F, Balduini CL. Eltrombopag for the treatment of the inherited thrombocytopenia deriving from MYH9 mutations. Blood 2010;116(26):5832-7.
Paviotti G, De Cunto A, Zennaro F, Boz G, Travan L, Cont G, Bua J, Demarini S. Higher growth, fat and fat-free masses correlate with larger cerebellar volumes in preterm infants at term. Acta Paediatr 2017;106(6):918-925.
Paviotti G, Demarini S, Verardi G, De Cunto A, Davanzo R. Making the first days of life safer: time for a new protocol?. J Perinatol 2014;34(12):957.

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