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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..
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..
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..
The diagnostic challenge of very early-onset enterocolitis in an infant with XIAP deficiency. BMC Pediatr 2015;15(1):208..
Genetic profile of patients with early onset inflammatory bowel disease. Gene 2018;645:18-29..
NLRP1 polymorphisms in patients with asbestos-associated mesothelioma. Infect Agent Cancer 2012;7(1):25..
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..
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..
Accuracy of diagnostic antibody tests for coeliac disease in children: summary of an evidence report. J Pediatr Gastroenterol Nutr 2012;54(2):229-41..
Combined use of AFM and soft X-ray microscopy to reveal fibres' internalization in mesothelial cells. Analyst 2017;142(11):1982-1992..
Mutations in TTC19 cause mitochondrial complex III deficiency and neurological impairment in humans and flies. Nat Genet 2011;43(3):259-63..
Severe X-linked mitochondrial encephalomyopathy associated with a mutation in apoptosis-inducing factor. Am J Hum Genet 2010;86(4):639-49..