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Pellegrin MChiara, Naviglio S, Cattaruzzi E, Barbi E, Ventura A. A Teenager with Sudden Unilateral Breast Enlargement. J Pediatr 2017;182:394.
Pellegrin MC, Matarazzo L, Neri E, Pennesi M, Crovella S. HLA-B35, a common genetic trait, in a familial case of Henoch-Schoenlein purpura and Berger's disease. Genet Mol Res 2014;13(2):2669-73.
Pelin M, De Iudicibus S, Fusco L, Taboga E, Pellizzari G, Lagatolla C, Martelossi S, Ventura A, Decorti G, Stocco G. Role of oxidative stress mediated by glutathione-s-transferase in thiopurines' toxic effects. Chem Res Toxicol 2015;28(6):1186-95.
Pelin M, De Iudicibus S, Londero M, Spizzo R, Rossi SDei, Martelossi S, Ventura A, Decorti G, Stocco G. Thiopurine Biotransformation and Pharmacological Effects: Contribution of Oxidative Stress. Curr Drug Metab 2016;17(6):542-9.
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, 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, Guida E, Maschio M, Rigamonti W, Gregori M, Codrich D. Handlebar injury in children: The hidden danger. Surgery 2015;
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, Barbi E, Zennaro F, Neri E. Fainting Starting Parenteral Nutrition. Pediatr Emerg Care 2015;31(9):648.
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;
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, Ma X, Savoia A, Adelstein RS. MYH9: Structure, functions and role of non-muscle myosin IIA in human disease. Gene 2018;664:152-167.

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