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Girotto G, Pirastu N, Sorice R, Biino G, Campbell H, d'Adamo AP, Hastie ND, Nutile T, Polasek O, Portas L, Rudan I, Ulivi S, Zemunik T, Wright AF, Ciullo M, Hayward C, Pirastu M, Gasparini P. Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathways. J Med Genet 2011;48(6):369-74.
Girardi D, Falco A, De Carlo A, Benevene P, Comar M, Tongiorgi E, Bartolucci GBattista. The mediating role of interpersonal conflict at work in the relationship between negative affectivity and biomarkers of stress. J Behav Med 2015;38(6):922-31.
Girardelli M, Bianco AM, Marcuzzi A, Crovella S. A comparative analysis of serologic parameters and oxidative stress in osteoarthritis and rheumatoid arthritis: reply to Mishra and colleagues. Rheumatol Int 2013;33(9):2445-6.
Girardelli M, Arrigo S, Barabino A, Loganes C, Morreale G, Crovella S, Tommasini A, Bianco AMonica. The diagnostic challenge of very early-onset enterocolitis in an infant with XIAP deficiency. BMC Pediatr 2015;15(1):208.
Girardelli M, Basaldella F, Paolera SDella, Vuch J, Tommasini A, Martelossi S, Crovella S, Bianco AMonica. Genetic profile of patients with early onset inflammatory bowel disease. Gene 2018;645:18-29.
Girardelli M, Maestri I, Rinaldi RR, Tognon M, Boldorini R, Bovenzi M, Crovella S, Comar M. NLRP1 polymorphisms in patients with asbestos-associated mesothelioma. Infect Agent Cancer 2012;7(1):25.
Girardelli M, Vuch J, Tommasini A, Crovella S, Bianco AMonica. Novel missense mutation in the NOD2 gene in a patient with early onset ulcerative colitis: causal or chance association?. Int J Mol Sci 2014;15(3):3834-41.
Giordano P, Saracco P, Grassi M, Luciani M, Banov L, Carraro F, Crocoli A, Cesaro S, Zanazzo GAndrea, Molinari AClaudio. Recommendations for the use of long-term central venous catheter (CVC) in children with hemato-oncological disorders: management of CVC-related occlusion and CVC-related thrombosis. On behalf of the coagulation defects working group and the supportive the. Ann Hematol 2015;94(11):1765-76.
Giersiepen K, Lelgemann M, Stuhldreher N, Ronfani L, Husby S, Koletzko S, Korponay-Szabó IR. Accuracy of diagnostic antibody tests for coeliac disease in children: summary of an evidence report. J Pediatr Gastroenterol Nutr 2012;54(2):229-41.
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.
Ghezzi D, Arzuffi P, Zordan M, Da Re C, Lamperti C, Benna C, d'Adamo P, Diodato D, Costa R, Mariotti C, Uziel G, Smiderle C, Zeviani M. Mutations in TTC19 cause mitochondrial complex III deficiency and neurological impairment in humans and flies. Nat Genet 2011;43(3):259-63.
Ghezzi D, Sevrioukova I, Invernizzi F, Lamperti C, Mora M, d'Adamo P, Novara F, Zuffardi O, Uziel G, Zeviani M. Severe X-linked mitochondrial encephalomyopathy associated with a mutation in apoptosis-inducing factor. Am J Hum Genet 2010;86(4):639-49.

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