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Molecular analysis of HEXA gene in Argentinean patients affected with Tay-Sachs disease: possible common origin of the prevalent c.459+5A>G mutation. Gene 2012;499(2):262-5.
. Molecular analysis of HEXA gene in Argentinean patients affected with Tay-Sachs disease: possible common origin of the prevalent c.459+5A>G mutation. Gene 2012;499(2):262-5.
. Molecular diagnosis of Usher syndrome: application of two different next generation sequencing-based procedures. PLoS One 2012;7(8):e43799.
. MYH9-related disorders: report on a patient of Greek origin presenting with macroscopic hematuria and presenile cataract, caused by an R1165C mutation. J Pediatr Hematol Oncol 2012;34(6):412-5.
. The negative prognostic value of TRAIL overexpression in oral squamous cell carcinomas does not preclude the potential therapeutic use of recombinant TRAIL. Invest New Drugs 2012;30(2):810-8.
. Peroxidase-like activity of ferruginous bodies isolated by exploiting their magnetic property. J Toxicol Environ Health A 2012;75(11):603-23.
. Polymorphisms in DC-SIGN and L-SIGN genes are associated with HIV-1 vertical transmission in a Northeastern Brazilian population. Hum Immunol 2012;73(11):1159-65.
. Potential role of TRAIL in the management of autoimmune diabetes mellitus. Curr Pharm Des 2012;18(35):5759-65.
. Recurrent fever and fitful abdominal pain in a child. Gastroenterology 2012;143(2):e11-2.
. RICH (rapidly involuting congenital hemangioma): not only a definition of wealth. J Pediatr 2012;161(2):365-365.e1.
. Sedation with intranasal midazolam of Angolan children undergoing invasive procedures. Acta Paediatr 2012;101(7):e296-8.
. Serum amyloid A and cholesterol: a pivotal role on inflammation. Amyloid 2012;19(3):163-4; author reply 165-6.
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