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Acute cardiac valvular involvement in Kawasaki Disease. Clin Exp Rheumatol 2011;29(1 Suppl 64):S140.
. HLA-B35, a common genetic trait, in a familial case of Henoch-Schoenlein purpura and Berger's disease. Genet Mol Res 2014;13(2):2669-73.
. Managing children under 36 months of age with febrile urinary tract infection: a new approach. Pediatr Nephrol 2012;27(4):611-5.
. Endoscopic treatment of primary vesicoureteral reflux. N Engl J Med 2012;367(1):88; author reply 89.
. Congenital aplasia of the optic chiasm and esophageal atresia: a case report. J Med Case Rep 2011;5:335.
. A Spotted Bone. J Pediatr 2016;176:220-220.e1.
. Genomic profiling by whole-genome single nucleotide polymorphism arrays in Wilms tumor and association with relapse. Genes Chromosomes Cancer 2012;51(7):644-53.
. TNF-related apoptosis inducing ligand in ocular cancers and ocular diabetic complications. Biomed Res Int 2015;2015:424019.
. 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.
. DNA mismatch repair gene MSH6 implicated in determining age at natural menopause. Hum Mol Genet 2014;23(9):2490-7.
. Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. Nature 2014;514(7520):92-7.
. Prevalence of celiac disease in patients with severe food allergy. Allergy 2015;70(10):1346-9.
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