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2015
Callea M, Willoughby CE, Nieminen P, Di Stazio M, Bellacchio E, Giglio S, Sani I, Vinciguerra A, Maglione M, Tadini G, Clarich G. Identification of a novel frameshift mutation in the EDAR gene causing autosomal dominant hypohidrotic ectodermal dysplasia. J Eur Acad Dermatol Venereol 2015;29(5):1032-4.
Tognon M, Luppi M, Corallini A, Taronna A, Barozzi P, Rotondo JCharles, Comar M, Casali MVittoria, Bovenzi M, D'Agostino A, Vinante F, Rigo A, Ferrarini I, Barbanti-Brodano G, Martini F, Mazzoni E. Immunologic evidence of a strong association between non-Hodgkin lymphoma and simian virus 40. Cancer 2015;121(15):2618-26.
Polesello V, Zupin L, Di Lenarda R, Biasotto M, Ottaviani G, Gobbo M, Cecco L, Alberi G, Pozzato G, Crovella S, Segat L. Impact of DEFB1 gene regulatory polymorphisms on hBD-1 salivary concentration. Arch Oral Biol 2015;60(7):1054-8.
De Cunto A, Paviotti G, Travan L, Bua J, Cont G, Demarini S. Impact of Surgery for Neonatal Gastrointestinal Diseases on Weight and Fat Mass. J Pediatr 2015;167(3):568-71.
Parodi A, Kalli F, Svahn J, Stroppiana G, De Rocco D, Terranova P, Dufour C, Fenoglio D, Cappelli E. Impaired immune response to Candida albicans in cells from Fanconi anemia patients. Cytokine 2015;73(1):203-7.
Huang J, Howie B, McCarthy S, Memari Y, Walter K, Min JL, Danecek P, Malerba G, Trabetti E, Zheng H-F, Gambaro G, J Richards B, Durbin R, Timpson NJ, Marchini J, Soranzo N. Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel. Nat Commun 2015;6:8111.
Mezzavilla M, Vozzi D, Badii R, Alkowari MKhalifa, Abdulhadi K, Girotto G, Gasparini P. Increased rate of deleterious variants in long runs of homozygosity of an inbred population from Qatar. Hum Hered 2015;79(1):14-9.
Faganello G, Fisicaro M, Russo G, Iorio A, Mazzone C, Grande E, Humar F, Cherubini A, Pandullo C, Barbati G, Tarantini L, Benettoni A, Pozzi M, Di Lenarda A, Cioffi G. Insights from Cardiac Mechanics after Three Decades from Successfully Repaired Aortic Coarctation. Congenit Heart Dis 2015;
Zupin L, Catamo E, Polesello V, Crovella S, Segat L. Interleukin-18 gene promoter polymorphisms and celiac disease in Italian patients. Mol Biol Rep 2015;42(2):525-33.
Angelo HD, Silva IIFGomes, Oliveira RDR, Louzada-Júnior P, Donadi EA, Crovella S, Maia MMD, de Souza PRE, Sandrin-Garcia P. Interleukin-18, interleukin-12B and interferon-γ gene polymorphisms in Brazilian patients with rheumatoid arthritis: a pilot study. Tissue Antigens 2015;86(4):276-8.
Clarici A, Pellizzoni S, Guaschino S, Alberico S, Bembich S, Giuliani R, Short A, Guarino G, Panksepp J. Intranasal adminsitration of oxytocin in postnatal depression: implications for psychodynamic psychotherapy from a randomized double-blind pilot study. Front Psychol 2015;6:426.
Maso G, Piccoli M, De Seta F, Parolin S, Banco R, L Mattos C, Bogatti P, Alberico S. Intrapartum fetal heart rate monitoring interpretation in labour: a critical appraisal. Minerva Ginecol 2015;67(1):65-79.

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