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Autore Titolo Tipo [ Anno(Asc)]
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2015
Chiurco A, Montico M, Brovedani P, Monasta L, Davanzo R. An IBCLC in the Maternity Ward of a Mother and Child Hospital: A Pre- and Post-Intervention Study. Int J Environ Res Public Health 2015;12(8):9938-51.
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.
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.
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.
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.
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.
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.
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;
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.

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