Export 46 results:
Autore Titolo Tipo [ Anno(Asc)]
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2016
Seraceni S, Campisciano G, Contini C, Comar M. HPV genotypes distribution in Chlamydia trachomatis co-infection in a large cohort of women from north-east Italy. J Med Microbiol 2016;65(5):406-13.
2015
Pederiva F, Guida E, Maschio M, Rigamonti W, Gregori M, Codrich D. Handlebar injury in children: The hidden danger. Surgery 2015;
Catamo E, Zupin L, Segat L, Celsi F, Crovella S. HLA-G and susceptibility to develop celiac disease. Hum Immunol 2015;76(1):36-41.
Lazzerini M, Sonego M, Pellegrin MChiara. Hypoxaemia as a Mortality Risk Factor in Acute Lower Respiratory Infections in Children in Low and Middle-Income Countries: Systematic Review and Meta-Analysis. PLoS One 2015;10(9):e0136166.
Scrimin F, Wiesenfeld U, Galati EF, Monasta L, Ricci G. Hysteroscopic chasing for endometrial cancer in a low-risk population: risks of overinvestigation. Arch Gynecol Obstet 2015;
2014
Ferrara G, Maximova N, Zennaro F, Gregori M, Tamaro P. Hematopoietic stem cell transplantation effects on spinal cord compression in Hurler. Pediatr Transplant 2014;18(3):E96-9.
Pastore S, Barbieri F, Di Leo G, Valencic E, Tommasini A, Ventura A. Hemophagocytic lymphohistiocytosis in total parenteral nutrition dependent children: description of 5 cases and practical tips for management. J Pediatr Hematol Oncol 2014;36(7):e440-2.
Vozzi D, Morgan A, Vuckovic D, D'Eustacchio A, Abdulhadi K, Rubinato E, Badii R, Gasparini P, Girotto G. Hereditary hearing loss: a 96 gene targeted sequencing protocol reveals novel alleles in a series of Italian and Qatari patients. Gene 2014;542(2):209-16.
Campioni D, Voltan R, Tisato V, Zauli G. Heterogeneity of mesenchymal stromal cells in lymphoproliferative disorders. Front Biosci (Landmark Ed) 2014;19:139-51.
Paviotti G, Bua J, De Cunto A, Travan L, Demarini S. High-frequency percussive ventilation as rescue treatment in severe hypoxemic respiratory failure in term neonates. J Crit Care 2014;29(4):662-3.
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.
Segat L, Zupin L, Kim H-Y, Catamo E, Thea DM, Kankasa C, Aldrovandi GM, Kuhn L, Crovella S. HLA-G 14 bp deletion/insertion polymorphism and mother-to-child transmission of HIV. Tissue Antigens 2014;83(3):161-7.

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