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A singular case of congenital self-healing histiocytosis with skin, liver and atypical eye involvement. Ocul Immunol Inflamm 2011;19(5):337-9.
. Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome. Nat Genet 2011;43(12):1256-61.
. Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome. Nat Genet 2011;43(12):1256-61.
. Splicing mutations in glycogen-storage disease type II: evaluation of the full spectrum of mutations and their relation to patients' phenotypes. Eur J Hum Genet 2011;19(4):422-31.
. Splicing mutations in glycogen-storage disease type II: evaluation of the full spectrum of mutations and their relation to patients' phenotypes. Eur J Hum Genet 2011;19(4):422-31.
. Successful treatment of acne with isotretinoin in chronic granulomatous disease. Eur J Dermatol 2011;21(1):111-2.
. Successful treatment of acne with isotretinoin in chronic granulomatous disease. Eur J Dermatol 2011;21(1):111-2.
. Thromboembolism in pediatric inflammatory bowel disease: systematic review. Inflamm Bowel Dis 2011;17(10):2174-83.
. Adverse effects during specific oral tolerance induction: in home phase. Allergol Immunopathol (Madr) 2012;40(1):41-50.
. Adverse effects during specific oral tolerance induction: in home phase. Allergol Immunopathol (Madr) 2012;40(1):41-50.
. Adverse effects during specific oral tolerance induction: in-hospital "rush" phase. Eur Ann Allergy Clin Immunol 2012;44(1):18-25.
. Adverse effects during specific oral tolerance induction: in-hospital "rush" phase. Eur Ann Allergy Clin Immunol 2012;44(1):18-25.
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