Export 19 results:
Autore Titolo Tipo [ Anno(Asc)]
Filtri: Autore è Girardelli, Martina  [Clear All Filters]
2018
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.
2016
Marcuzzi A, Piscianz E, Zweyer M, Bortul R, Loganes C, Girardelli M, Baj G, Monasta L, Celeghini C. Geranylgeraniol and Neurological Impairment: Involvement of Apoptosis and Mitochondrial Morphology. Int J Mol Sci 2016;17(3):365.
Kamada AJ, Bianco AM, Zupin L, Girardelli M, Matte MCC, de Medeiros RMarília, Almeida SEsteves de, Rocha MM, Segat L, Chies JAB, Kuhn L, Crovella S. Protective Role of BST2 Polymorphisms in Mother-to-Child Transmission of HIV-1 and Adult AIDS Progression. J Acquir Immune Defic Syndr 2016;72(3):237-41.
Marcuzzi A, Vozzi D, Girardelli M, Tricarico PMaura, Knowles A, Crovella S, Vuch J, Tommasini A, Piscianz E, Bianco AMonica. Putative modifier genes in mevalonate kinase deficiency. Mol Med Rep 2016;13(4):3181-9.
2015
Tricarico PMaura, Girardelli M, Kleiner G, Knowles A, Valencic E, Crovella S, Marcuzzi A. Alendronate, a double-edged sword acting in the mevalonate pathway. Mol Med Rep 2015;12(3):4238-42.
Lougaris V, Faletra F, Lanzi G, Vozzi D, Marcuzzi A, Valencic E, Piscianz E, Bianco AM, Girardelli M, Baronio M, Loganes C, Fasth A, Salvini F, Trizzino A, Moratto D, Facchetti F, Giliani S, Plebani A, Tommasini A. Altered germinal center reaction and abnormal B cell peripheral maturation in PI3KR1-mutated patients presenting with HIGM-like phenotype. Clin Immunol 2015;159(1):33-6.
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.
Bianco AMonica, Girardelli M, Tommasini A. Genetics of inflammatory bowel disease from multifactorial to monogenic forms. World J Gastroenterol 2015;21(43):12296-310.
Bianco AMonica, Faletra F, Vozzi D, Girardelli M, Knowles A, Tommasini A, Zauli G, Marcuzzi A. 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.
2014
Tricarico PMaura, Kleiner G, Valencic E, Campisciano G, Girardelli M, Crovella S, Knowles A, Marcuzzi A. Block of the mevalonate pathway triggers oxidative and inflammatory molecular mechanisms modulated by exogenous isoprenoid compounds. Int J Mol Sci 2014;15(4):6843-56.
Brumatti LVecchi, Marcuzzi A, Tricarico PMaura, Zanin V, Girardelli M, Bianco AMonica. Curcumin and inflammatory bowel disease: potential and limits of innovative treatments. Molecules 2014;19(12):21127-53.
Bianco AMonica, Girardelli M, Vozzi D, Crovella S, Kleiner G, Marcuzzi A. Mevalonate kinase deficiency and IBD: shared genetic background. Gut 2014;63(8):1367-8.

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