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Magnolato A, Pederiva F, Spagnut G, Maschio M, Ventura A, Taddio A. Three cases of Bartonella quintana infection in children. Pediatr Infect Dis J 2015;34(5):540-2.
Magurano F, Baggieri M, Filia A, Del Manso M, Lazzarotto T, Amendola A, D'Agaro P, Chironna M, Ansaldi F, Iannazzo S, Bucci P, Marchi A, Nicoletti L. Towards measles elimination in Italy: Virological surveillance and genotypes trend (2013-2015). Virus Res 2017;236:24-29.
Makar AB, McMartin KE, Palese M, Tephly TR. Formate assay in body fluids: application in methanol poisoning. Biochem Med 1975;13(2):117-26.
Manara R, D'Agata L, Rocco MC, Cusmai R, Freri E, Pinelli L, Darra F, Procopio E, Mardari R, Zanus C, Di Rosa G, Soddu C, Severino M, Ermani M, Longo D, Sartori S. Neuroimaging Changes in Menkes Disease, Part 1. AJNR Am J Neuroradiol 2017;38(10):1850-1857.
Mancini C, Giorgio E, Rubegni A, Pradotto L, Bagnoli S, Rubino E, Prontera P, Cavalieri S, Di Gregorio E, Ferrero M, Pozzi E, Riberi E, Ferrero P, Nigro P, Mauro A, Zibetti M, Tessa A, Barghigiani M, Antenora A, Sirchia F, Piacentini S, Silvestri G, De Michele G, Filla A, Orsi L, Santorelli FM, Brusco A. Prevalence and phenotype of the c.1529C>T SPG7 variant in adult-onset cerebellar ataxia in Italy. Eur J Neurol 2019;26(1):80-86.
Mandalà M, Muzzi E, Trabalzini F. Giant Cerebellar Lesion in a Patient With Purulent Ear Drainage. JAMA Otolaryngol Head Neck Surg 2016;142(6):603-4.
Mangogna A, Belmonte B, Agostinis C, Ricci G, Gulino A, Ferrara I, Zanconati F, Tripodo C, Romano F, Kishore U, Bulla R. Pathological Significance and Prognostic Value of Surfactant Protein D in Cancer. Front Immunol 2018;9:1748.
Manna F, Barbi E, Murru F, Bussani R. Lingual schwannoma in pediatric patients. J Craniofac Surg 2012;23(5):e454-6.
Mantero E, Carbone M, Calevo MG, Boero S. Diagnosis and treatment of pediatric chronic osteomyelitis in developing countries: prospective study of 96 patients treated in Kenya. Musculoskelet Surg 2011;95(1):13-8.
Maranhão RM de Albuq, Esteves FAMartins, Crovella S, Segat L, Souza PREleutér. Tumor necrosis factor-α and interleukin-6 gene polymorphism association with susceptibility to celiac disease in Italian patients. Genet Mol Res 2015;14(4):16343-52.
Marchetti F, Bua J, Tornese G, Piras G, Toffol G, Ronfani L. Management of cryptorchidism: a survey of clinical practice in Italy. BMC Pediatr 2012;12:4.
Marconi C, Di Buduo CA, LeVine K, Barozzi S, Faleschini M, Bozzi V, Palombo F, McKinstry S, Lassandro G, Giordano P, Noris P, Balduini CL, Savoia A, Balduini A, Pippucci T, Seri M, Katsanis N, Pecci A. Loss-of-function mutations in cause a new form of inherited thrombocytopenia. Blood 2019;133(12):1346-1357.

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