Drupal-Biblio17<style face="normal" font="default" size="100%">Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Needle-related pain and distress management during needle-related procedures in children with and without intellectual disability.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Neuronal Dysfunction Associated with Cholesterol Deregulation.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">A new form of inherited thrombocytopenia due to monoallelic loss of function mutation in the thrombopoietin gene.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Non-invasive biomarkers of fetal brain development reflecting prenatal stress: An integrative multi-scale multi-species perspective on data collection and analysis.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Novel genetic associations for blood pressure identified via gene-alcohol interaction in up to 570K individuals across multiple ancestries.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Nutrient intakes in an Italian population of infants during the complementary feeding period.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Natalizumab treatment of multiple sclerosis: new insights.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Neuroimaging Changes in Menkes Disease, Part 1.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Novel Blood Pressure Locus and Gene Discovery Using Genome-Wide Association Study and Expression Data Sets From Blood and the Kidney.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">A Novel Panel of Serum Biomarkers for MPM Diagnosis.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Nationwide study of headache pain in Italy shows that pain assessment is still inadequate in paediatric emergency care.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Non-additive genome-wide association scan reveals a new gene associated with habitual coffee consumption.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Nonmuscle Myosin Heavy Chain IIA Mutation Predicts Severity and Progression of Sensorineural Hearing Loss in Patients With MYH9-Related Disease.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Nasal irrigation with saline solution significantly improves oxygen saturation in infants with bronchiolitis.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">A nationwide survey of PMM2-CDG in Italy: high frequency of a mild neurological variant associated with the L32R mutation.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">New genetic loci link adipose and insulin biology to body fat distribution.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">New lenses to look at preeclampsia.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Next-generation sequencing and its initial applications for molecular diagnosis of systemic auto-inflammatory diseases.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">NLRP1 and NLRP3 polymorphisms in mesothelioma patients and asbestos exposed individuals a population-based autopsy study from North East Italy.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Normal saline flushes performed once daily maintain peripheral intravenous catheter patency: a randomised controlled trial.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">The novel dual PI3K/mTOR inhibitor NVP-BGT226 displays cytotoxic activity in both normoxic and hypoxic hepatocarcinoma cells.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">A neonate with a 'milky' blood. What can it be?</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Neutralizing and IgG antibodies against simian virus 40 in healthy pregnant women in Italy.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Next generation sequencing in nonsyndromic intellectual disability: from a negative molecular karyotype to a possible causative mutation detection.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">NF-κB pathways in hematological malignancies.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">NLRP3 polymorphism is associated with protection against human T-lymphotropic virus 1 infection.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">No evidence of Polyomavirus and EBV infections in Italian patients with mixed cryoglobulinemia infected chronically with HCV.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Non-classical MHC-I human leukocyte antigen (HLA-G) in hepatotropic viral infections and in hepatocellular carcinoma.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">A non-complement-fixing antibody to β2 glycoprotein I as a novel therapy for antiphospholipid syndrome.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">A novel deletion mutation involving TMEM38B in a patient with autosomal recessive osteogenesis imperfecta.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Novel missense mutation in the NOD2 gene in a patient with early onset ulcerative colitis: causal or chance association?</style>Drupal-Biblio17<style face="normal" font="default" size="100%">A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">The non-genotoxic activator of the p53 pathway Nutlin-3 shifts the balance between E2F7 and E2F1 transcription factors in leukemic cells.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">A novel CRYBB2 missense mutation causing congenital autosomal dominant cataract in an Italian family.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">NALP1/NLRP1 genetic variants are associated with Alzheimer disease.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">The negative prognostic value of TRAIL overexpression in oral squamous cell carcinomas does not preclude the potential therapeutic use of recombinant TRAIL.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">New insights in the sugarcane transcriptome responding to drought stress as revealed by superSAGE.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">NF-κB as a target for modulating inflammatory responses.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">NLRP1 polymorphisms in patients with asbestos-associated mesothelioma.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Nutlin-3 differentially modulates miRNA34a and miRNA181 versus miR26a and miR155 in p53 proficient and p53 deficient B chronic lymphocytic leukemia (B-CLL) samples.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Neonatal necrotizing tracheobronchitis.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Neuromotor deficits in developmental coordination disorder: evidence from a reach-to-grasp task.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">A new case of duplication of the MDS region identified by high-density SNP arrays and a review of the literature.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Non-invasive assessment of hemispheric language dominance by optical topography during a brief passive listening test: a pilot study.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Natural isoprenoids inhibit LPS-induced-production of cytokines and nitric oxide in aminobisphosphonate-treated monocytes.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Neonatal jaundice and breastfeeding reputation.</style>