Export 1151 results:
Autore Titolo Tipo [ Anno(Asc)]
Filtri: Filter è   [Clear All Filters]
2017
Callea M, Cammarata-Scalisi F, Willoughby CE, Giglio SR, Sani I, Bargiacchi S, Traficante G, Bellacchio E, Tadini G, Yavuz I, Galeotti A, Clarich G. [Clinical and molecular study in a family with autosomal dominant hypohidrotic ectodermal dysplasia]. Arch Argent Pediatr 2017;115(1):e34-e38.
Gianoncelli A, Kourousias G, Cammisuli F, Cassese D, Rizzardi C, Radillo O, Lazzarino M, Pascolo L. Combined use of AFM and soft X-ray microscopy to reveal fibres' internalization in mesothelial cells. Analyst 2017;142(11):1982-1992.
Corre T, Olinger E, Harris SE, Traglia M, Ulivi S, Lenarduzzi S, Belge H, Youhanna S, Tokonami N, Bonny O, Houillier P, Polasek O, Deary IJ, Starr JM, Toniolo D, Gasparini P, Vollenweider P, Hayward C, Bochud M, Devuyst O. Common variants in CLDN14 are associated with differential excretion of magnesium over calcium in urine. Pflugers Arch 2017;469(1):91-103.
Maximova N, Schillani G, Simeone R, Maestro A, Zanon D. Comparison of Efficacy and Safety of Caspofungin Versus Micafungin in Pediatric Allogeneic Stem Cell Transplant Recipients: A Retrospective Analysis. Adv Ther 2017;34(5):1184-1199.
Agostinis C, Vidergar R, Belmonte B, Mangogna A, Amadio L, Geri P, Borelli V, Zanconati F, Tedesco F, Confalonieri M, Tripodo C, Kishore U, Bulla R. Complement Protein C1q Binds to Hyaluronic Acid in the Malignant Pleural Mesothelioma Microenvironment and Promotes Tumor Growth. Front Immunol 2017;8:1559.
Villa N, Conconi D, D Benussi G, Tornese G, Crosti F, Sala E, Dalprà L, Pecile V. A complete duplication of X chromosome resulting in a tricentric isochromosome originated by centromere repositioning. Mol Cytogenet 2017;10:22.
Matarazzo L, Delise A, Zennaro F, Bussani R, Demarini S, Berti I, Ventura A. A congenital purplish tumour. Arch Dis Child Educ Pract Ed 2017;102(2):79-81.
Biffi S, Andolfi L, Caltagirone C, Garrovo C, Falchi AM, Lippolis V, Lorenzon A, Macor P, Meli V, Monduzzi M, Obiols-Rabasa M, Petrizza L, Prodi L, Rosa A, Schmidt J, Talmon Y, Murgia S. Cubosomes for in vivo fluorescence lifetime imaging. Nanotechnology 2017;28(5):055102.
Loganes C, Lega S, Bramuzzo M, Brumatti LVecchi, Piscianz E, Valencic E, Tommasini A, Marcuzzi A. Curcumin Anti-Apoptotic Action in a Model of Intestinal Epithelial Inflammatory Damage. Nutrients 2017;9(6)
Llop S, Tran V, Ballester F, Barbone F, Sofianou-Katsoulis A, Sunyer J, Engström K, Alhamdow A, Love TM, Watson GE, Bustamante M, Murcia M, Iñiguez C, Shamlaye CF, Rosolen V, Mariuz M, Horvat M, Tratnik JS, Mazej D, van Wijngaarden E, Davidson PW, Myers GJ, Rand MD, Broberg K. CYP3A genes and the association between prenatal methylmercury exposure and neurodevelopment. Environ Int 2017;105:34-42.
Polesello V, Zupin L, Di Lenarda R, Biasotto M, Pozzato G, Ottaviani G, Gobbo M, Crovella S, Segat L. DEFB1 polymorphisms and salivary hBD-1 concentration in Oral Lichen Planus patients and healthy subjects. Arch Oral Biol 2017;73:161-165.
Cappelli E, Cuccarolo P, Stroppiana G, Miano M, Bottega R, Cossu V, Degan P, Ravera S. Defects in mitochondrial energetic function compels Fanconi Anaemia cells to glycolytic metabolism. Biochim Biophys Acta Mol Basis Dis 2017;1863(6):1214-1221.

Amministrazione Trasparente