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Zanin V, Segat L, Bianco AMonica, Padovan L, Tavares Nde Alencar, Crovella S. DEFB1 gene 5' untranslated region (UTR) polymorphisms in inflammatory bowel diseases. Clinics (Sao Paulo) 2012;67(4):395-8.
Secchiero P, Perri P, Melloni E, Martini A, Lamberti G, Sebastiani A, Zauli G. Decreased levels of soluble TNF-related apoptosis-inducing ligand (TRAIL) in the conjunctival sac fluid of patients with diabetes affected by proliferative retinopathy. Diabet Med 2011;28(10):1277-8.
Marcuzzi A, Decorti G, Pontillo A, Ventura A, Tommasini A. Decreased cholesterol levels reflect a consumption of anti-inflammatory isoprenoids associated with an impaired control of inflammation in a mouse model of mevalonate kinase deficiency. Inflamm Res 2010;59(5):335-8.
Floridia M, Tamburrini E, Anzidei G, Tibaldi C, Muggiasca ML, Guaraldi G, Fiscon M, Vimercati A, Martinelli P, Donisi A, Dalzero S, Ravizza M. Declining HCV seroprevalence in pregnant women with HIV. Epidemiol Infect 2010;138(9):1317-21.
Bibalo C, Longo G, Ventura A. Decline in Lung Function in Childhood Asthma. N Engl J Med 2016;375(7):e13.
Taddio A, Rosé C, Lepore L, Ventura A. Dealing with abdominal pain in children affected by systemic lupus erythematosus. Semin Arthritis Rheum 2012;41(4):e3-4.
Bonaglia MClara, Kurtas NEdibe, Errichiello E, Bertuzzo S, Beri S, Mehrjouy MM, Provenzano A, Vergani D, Pecile V, Novara F, Reho P, Di Giacomo MCarmela, Discepoli G, Giorda R, Aldred MA, Santos-Rebouças CBarros, Goncalves APereira, Abuelo DN, Giglio S, Ricca I, Franchi F, Patsalis P, Sismani C, Morí MAngeles, Nevado J, Tommerup N, Zuffardi O. De novo unbalanced translocations have a complex history/aetiology. Hum Genet 2018;137(10):817-829.
Perrone MD, Rocca MS, Bruno I, Faletra F, Pecile V, Gasparini P. De novo 911 Kb interstitial deletion on chromosome 1q43 in a boy with mental retardation and short stature. Eur J Med Genet 2012;55(2):117-9.
Fabretto A, Rocca MSanta, Perrone MDolores, Skabar A, Pecile V, Gasparini P. De novo 6.9 Mb interstitial deletion on chromosome 4q31.1-q32.1 in a girl with severe speech delay and dysmorphic features. Am J Med Genet A 2012;158A(4):882-7.
da Silva RCelerino, Tavares Nde Alencar, Moura R, Coelho A, Guimarães RLima, Araújo J, Crovella S, Brandão LAndré Cav, Silva Jde Azevêd. DC-SIGN polymorphisms are associated to type 1 diabetes mellitus. Immunobiology 2014;219(11):859-65.
Zauli G, Voltan R, Bosco R, Melloni E, Marmiroli S, Rigolin GMatteo, Cuneo A, Secchiero P. Dasatinib plus Nutlin-3 shows synergistic antileukemic activity in both p53 wild-type and p53 mutated B chronic lymphocytic leukemias by inhibiting the Akt pathway. Clin Cancer Res 2011;17(4):762-70.
Wolfler A, Calderoni E, Ottonello G, Conti G, Baroncini S, Santuz P, Vitale P, Salvo I. Daily practice of mechanical ventilation in Italian pediatric intensive care units: a prospective survey. Pediatr Crit Care Med 2011;12(2):141-6.

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