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Autore Titolo Tipo [ Anno(Asc)]
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2016
Di Sabatino A, Giuffrida P, Fornasa G, Salvatore C, Vanoli A, Naviglio S, De Leo L, Pasini A, De Amici M, Alvisi C, Not T, Rescigno M, Corazza GRoberto. Innate and adaptive immunity in self-reported nonceliac gluten sensitivity versus celiac disease. Dig Liver Dis 2016;48(7):745-52.
Di Sabatino A, Giuffrida P, Fornasa G, Salvatore C, Vanoli A, Naviglio S, De Leo L, Pasini A, De Amici M, Alvisi C, Not T, Rescigno M, Corazza GRoberto. Innate and adaptive immunity in self-reported nonceliac gluten sensitivity versus celiac disease. Dig Liver Dis 2016;48(7):745-52.
Di Sabatino A, Giuffrida P, Fornasa G, Salvatore C, Vanoli A, Naviglio S, De Leo L, Pasini A, De Amici M, Alvisi C, Not T, Rescigno M, Corazza GRoberto. Innate and adaptive immunity in self-reported nonceliac gluten sensitivity versus celiac disease. Dig Liver Dis 2016;48(7):745-52.
Travan L, Naviglio S, Cont G, Brovedani P, Davanzo R, Demarini S. Isolated hypoplasia of abdominal wall muscles associated with fetal ascites. Congenit Anom (Kyoto) 2016;56(4):184-186.
Travan L, Naviglio S, Cont G, Brovedani P, Davanzo R, Demarini S. Isolated hypoplasia of abdominal wall muscles associated with fetal ascites. Congenit Anom (Kyoto) 2016;56(4):184-186.
Rocca MS, Pecile V, Cleva L, Speltra E, Selice R, Di Mambro A, Foresta C, Ferlin A. The Klinefelter syndrome is associated with high recurrence of copy number variations on the X chromosome with a potential role in the clinical phenotype. Andrology 2016;4(2):328-34.
Ziberna F, De Lorenzo G, Schiavon V, Arnoldi F, Quaglia S, De Leo L, Vatta S, Martelossi S, Burrone OR, Ventura A, Not T. Lack of Evidence of Rotavirus-Dependent Molecular Mimicry as a Trigger of Celiac Disease. Clin Exp Immunol 2016;
Ziberna F, De Lorenzo G, Schiavon V, Arnoldi F, Quaglia S, De Leo L, Vatta S, Martelossi S, Burrone OR, Ventura A, Not T. Lack of Evidence of Rotavirus-Dependent Molecular Mimicry as a Trigger of Celiac Disease. Clin Exp Immunol 2016;
Nicchia E, Giordano P, Greco C, De Rocco D, Savoia A. Molecular diagnosis of thrombocytopenia-absent radius syndrome using next-generation sequencing. Int J Lab Hematol 2016;38(4):412-8.
Russo S, Calzari L, Mussa A, Mainini E, Cassina M, Di Candia S, Clementi M, Guzzetti S, Tabano S, Miozzo M, Sirchia S, Finelli P, Prontera P, Maitz S, Sorge G, Calcagno A, Maghnie M, Divizia MTeresa, Melis D, Manfredini E, Ferrero GBattista, Pecile V, Larizza L. A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes. Clin Epigenetics 2016;8:23.
Russo S, Calzari L, Mussa A, Mainini E, Cassina M, Di Candia S, Clementi M, Guzzetti S, Tabano S, Miozzo M, Sirchia S, Finelli P, Prontera P, Maitz S, Sorge G, Calcagno A, Maghnie M, Divizia MTeresa, Melis D, Manfredini E, Ferrero GBattista, Pecile V, Larizza L. A multi-method approach to the molecular diagnosis of overt and borderline 11p15.5 defects underlying Silver-Russell and Beckwith-Wiedemann syndromes. Clin Epigenetics 2016;8:23.
Wanderley-Nogueira ACarolina, Bezerra-Neto JPacífico, Kido ÉAkio, de Araújo FTadeu, Amorim LLindinalva, Crovella S, Benko-Iseppon AMaria. Plant Elite Squad: First Defense Line and Resistance Genes - Identification, Diversity and Functional Roles. Curr Protein Pept Sci 2016;

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