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Filtri: Autore è Bianco, Anna Monica [Clear All Filters]
Genetic profile of patients with early onset inflammatory bowel disease. Gene 2018;645:18-29.
. Iron signature in asbestos-induced malignant pleural mesothelioma: A population-based autopsy study. J Toxicol Environ Health A 2016;79(3):129-41.
. Putative modifier genes in mevalonate kinase deficiency. Mol Med Rep 2016;13(4):3181-9.
. The diagnostic challenge of very early-onset enterocolitis in an infant with XIAP deficiency. BMC Pediatr 2015;15(1):208.
. Fever tree revisited: From malaria to autoinflammatory diseases. World J Clin Pediatr 2015;4(4):106-12.
. Genetics of inflammatory bowel disease from multifactorial to monogenic forms. World J Gastroenterol 2015;21(43):12296-310.
. Two‑gene mutation in a single patient: Biochemical and functional analysis for a correct interpretation of exome results. Mol Med Rep 2015;12(4):6128-32.
. Curcumin and inflammatory bowel disease: potential and limits of innovative treatments. Molecules 2014;19(12):21127-53.
. F402L variant in NLRP12 in subjects with undiagnosed periodic fevers and in healthy controls. Clin Exp Rheumatol 2014;32(6):993-4.
. Mevalonate kinase deficiency and IBD: shared genetic background. Gut 2014;63(8):1367-8.
. 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.
. Family history in early-onset inflammatory bowel disease. J Gastroenterol 2013;48(1):144.
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