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MYH9-related disease: Report on five German families and description of a novel mutation. Ann Hematol 2010;89(10):1057-9.
. MYH9-related disease: Report on five German families and description of a novel mutation. Ann Hematol 2010;89(10):1057-9.
. Pharmacogenomics in pediatric leukemia. Curr Opin Pediatr 2010;22(6):703-10.
. Predictors of poor response to methotrexate in polyarticular-course juvenile idiopathic arthritis: analysis of the PRINTO methotrexate trial. Ann Rheum Dis 2010;69(8):1479-83.
. Severe X-linked mitochondrial encephalomyopathy associated with a mutation in apoptosis-inducing factor. Am J Hum Genet 2010;86(4):639-49.
. Splenomegaly as presentation of a wandering spleen. J Pediatr 2010;157(5):859.e1.
. State of the art and recommendations. Kangaroo mother care: application in a high-tech environment. Breastfeed Rev 2010;18(3):21-8.
. State of the art and recommendations. Kangaroo mother care: application in a high-tech environment. Acta Paediatr 2010;99(6):812-9.
. [Strategies for cardiovascular prevention in children]. G Ital Cardiol (Rome) 2010;11(5 Suppl 3):87S-89S.
. Structural aspects of plant antimicrobial peptides. Curr Protein Pept Sci 2010;11(3):210-9.
. Therapeutic strategy in p47-phox deficient chronic granulomatous disease presenting as inflammatory bowel disease. J Allergy Clin Immunol 2010;125(4):943-946.e1.
. Therapeutic strategy in p47-phox deficient chronic granulomatous disease presenting as inflammatory bowel disease. J Allergy Clin Immunol 2010;125(4):943-946.e1.
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