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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.
. NALP1/NLRP1 genetic variants are associated with Alzheimer disease. Alzheimer Dis Assoc Disord 2012;26(3):277-81.
. 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.
. New insights in the sugarcane transcriptome responding to drought stress as revealed by superSAGE. ScientificWorldJournal 2012;2012:821062.
. Oral rehabilitation of children with ectodermal dysplasia. BMJ Case Rep 2012;2012
. Pathergy as a cause of false-positive tuberculin skin test. Pediatr Infect Dis J 2012;31(1):104.
. Phylloid pattern of hypomelanosis closely related to chromosomal abnormalities in the 13q detected by SNP array analysis. Dermatology 2012;225(4):294-7.
. Polimorphisms in inflammasome genes are involved in the predisposition to systemic lupus erythematosus. Autoimmunity 2012;45(4):271-8.
. Polimorphisms in inflammasome genes are involved in the predisposition to systemic lupus erythematosus. Autoimmunity 2012;45(4):271-8.
. Polymorphisms in inflammasome' genes and susceptibility to HIV-1 infection. J Acquir Immune Defic Syndr 2012;59(2):121-5.
. A real-time polymerase chain reaction-based protocol for low/medium-throughput Y-chromosome microdeletions analysis. Genet Test Mol Biomarkers 2012;16(12):1349-55.
. A real-time polymerase chain reaction-based protocol for low/medium-throughput Y-chromosome microdeletions analysis. Genet Test Mol Biomarkers 2012;16(12):1349-55.
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