Export 21 results:
Autore Titolo Tipo [ Anno] Filtri: Autore è Bianco, Anna Monica [Clear All Filters]
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.
. 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.
. 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.
. Genetic profile of patients with early onset inflammatory bowel disease. Gene 2018;645:18-29.
.