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Pernambuco).</style>Drupal-Biblio17<style face="normal" font="default" size="100%">A case of lymphedema-distichiasis syndrome carrying a new de novo frameshift FOXC2 mutation.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Declining HCV seroprevalence in pregnant women with HIV.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Eltrombopag for the treatment of the inherited thrombocytopenia deriving from MYH9 mutations.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Emx2 and Foxg1 inhibit gliogenesis and promote neuronogenesis.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">EULAR/PRINTO/PRES criteria for Henoch-Schönlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part I: Overall methodology and clinical characterisation.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">First case in Italy of acquired resistance to oseltamivir in an immunocompromised patient with influenza A/H1N1v infection.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Five new OTOF gene mutations and auditory neuropathy.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">A G to C transversion at the last nucleotide of exon 25 of the MYH9 gene results in a missense mutation rather than in a splicing defect.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Hepatic glycogenosis in an adolescent with diabetes.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">HLA-G*0105N allele is associated with augmented risk for HIV infection in white female patients.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">[Human papillomavirus cervical infection: viral genotyping and risk factors for high-grade squamous intraepithelial lesion and cervix cancer].</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Incidence of bacteremias and invasive mycoses in children with acute non-lymphoblastic leukemia: results from a multi-center Italian study.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Long-term observational, non-randomized study of enzyme replacement therapy in late-onset glycogenosis type II.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Methotrexate withdrawal at 6 vs 12 months in juvenile idiopathic arthritis in remission: a randomized clinical trial.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Modeling the effect of 3 missense AGXT mutations on dimerization of the AGT enzyme in primary hyperoxaluria type 1.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Molecular surveillance of pandemic influenza A(H1N1) viruses circulating in Italy from May 2009 to February 2010: association between haemagglutinin mutations and clinical outcome.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Morbidity of pandemic H1N1 influenza in children with cancer.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Multidrug resistant Pseudomonas aeruginosa infection in children undergoing chemotherapy and hematopoietic stem cell transplantation.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Predictors of poor response to methotrexate in polyarticular-course juvenile idiopathic arthritis: analysis of the PRINTO methotrexate trial.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Screening for GJB2 and GJB6 gene mutations in patients from Campania region with sensorineural hearing loss.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Therapeutic strategy in p47-phox deficient chronic granulomatous disease presenting as inflammatory bowel disease.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Transmission of hemagglutinin D222G mutant strain of pandemic (H1N1) 2009 virus.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Treatment with recombinant tumor necrosis factor-related apoptosis-inducing ligand alleviates the severity of streptozotocin-induced diabetes.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Two cases of Noonan syndrome with severe respiratory and gastroenteral involvement and the SOS1 mutation F623I.</style>