Drupal-Biblio17<style face="normal" font="default" size="100%">An evaluation of the Movement ABC-2 Test for use in Italy: A comparison of data from Italy and the UK.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Anti-transglutaminase 6 Antibody Development in Children With Celiac Disease Correlates With Duration of Gluten Exposure.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Exome-chip meta-analysis identifies novel loci associated with cardiac conduction, including ADAMTS6.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genome Analyses of >200,000 Individuals Identify 58 Loci for Chronic Inflammation and Highlight Pathways that Link Inflammation and Complex Disorders.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genome-wide association meta-analysis of individuals of European ancestry identifies new loci explaining a substantial fraction of hair color variation and heritability.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">A genome-wide association study of corneal astigmatism: The CREAM Consortium.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Joint Data Analysis in Nutritional Epidemiology: Identification of Observational Studies and Minimal Requirements.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">A Large-Scale Multi-ancestry Genome-wide Study Accounting for Smoking Behavior Identifies Multiple Significant Loci for Blood Pressure.</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%">PR interval genome-wide association meta-analysis identifies 50 loci associated with atrial and atrioventricular electrical activity.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">What is the quality of the maternal near-miss case reviews in WHO European Region? Cross-sectional study in Armenia, Georgia, Latvia, Republic of Moldova and Uzbekistan.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">1000 Genomes-based meta-analysis identifies 10 novel loci for kidney function.</style>Drupal-Biblio17<style face="normal" font="default" size="100%"> and Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Antibiotic Prophylaxis for Urinary Tract Infection-Related Renal Scarring: A Systematic Review.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Child and Adolescent Health From 1990 to 2015: Findings From the Global Burden of Diseases, Injuries, and Risk Factors 2015 Study.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Climate change, emerging infections and blood donations.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Common variants in CLDN14 are associated with differential excretion of magnesium over calcium in urine.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">CYP3A genes and the association between prenatal methylmercury exposure and neurodevelopment.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Early-life nutritional exposures and lifelong health: immediate and long-lasting impacts of probiotics, vitamin D, and breastfeeding.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Fetal monitoring indications for delivery and 2-year outcome in 310 infants with fetal growth restriction delivered before 32 weeks' gestation in the TRUFFLE study.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genetic structure in the Sherpa and neighboring Nepalese populations.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genome-wide association analysis identifies novel blood pressure loci and offers biological insights into cardiovascular risk.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Gray platelet syndrome: Novel mutations of the NBEAL2 gene.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">How to monitor pregnancies complicated by fetal growth restriction and delivery before 32 weeks: post-hoc analysis of TRUFFLE study.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Immediate delivery or expectant management in gestational diabetes at term: the GINEXMAL randomised controlled trial.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">ISL1 is a major susceptibility gene for classic bladder exstrophy and a regulator of urinary tract development.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Longitudinal study of computerized cardiotocography in early fetal growth restriction.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Metastatic neuroblastoma in infants: are survival rates excellent only within the stringent framework of clinical trials?</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Mutations of RUNX1 in families with inherited thrombocytopenia.</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%">Rare and low-frequency coding variants alter human adult height.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Safety and effectiveness of oral propranolol for infantile hemangiomas started before 5 weeks and after 5 months of age: an Italian multicenter experience.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Targeted sequencing identifies novel variants involved in autosomal recessive hereditary hearing loss in Qatari families.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Training in Occupational Medicine: Jurisprudential Malfunctions in the Italian System and European Perspectives.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Association between p21 Ser31Arg polymorphism and the development of cervical lesion in women infected with high risk HPV.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">CCR2 and CCR5 genes polymorphisms in women with cervical lesions from Pernambuco, Northeast Region of Brazil: a case-control study.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Circulating levels of TNF-related apoptosis inducing-ligand are decreased in patients with large adult-type granulosa cell tumors-implications for therapeutic potential.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">CNV analysis in 169 patients with bladder exstrophy-epispadias complex.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Consensus Conference on Clinical Management of pediatric Atopic Dermatitis.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">EPG5-related Vici syndrome: a paradigm of neurodevelopmental disorders with defective autophagy.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genome-wide association study identifies 74 loci associated with educational attainment.</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%">A reference panel of 64,976 haplotypes for genotype imputation.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Somatic, hematologic phenotype, long-term outcome, and effect of hematopoietic stem cell transplantation. 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repair.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">MID2 can substitute for MID1 and control exocytosis of lytic granules in cytotoxic T cells.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Modulation of genetic associations with serum urate levels by body-mass-index in humans.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Multicohort analysis of the maternal age effect on recombination.</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%">Population genetic differentiation of height and body mass index across Europe.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Rare coding variants and X-linked loci associated with age at menarche.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">A Sensitive Electrochemiluminescence Immunosensor for Celiac Disease Diagnosis Based on Nanoelectrode Ensembles.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Tumor necrosis factor (TNF) alpha and interleukin (IL) 18 genes polymorphisms are correlated with susceptibility to HPV infection in patients with and without cervical intraepithelial lesion.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopenia.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Common variants in UMOD associate with urinary uromodulin levels: a meta-analysis.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">DNA mismatch repair gene MSH6 implicated in determining age at natural menopause.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">A general approach for haplotype phasing across the full spectrum of relatedness.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genome-wide association study of sexual maturation in males and females highlights a role for body mass and menarche loci in male puberty.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Global, regional, and national incidence and mortality for HIV, tuberculosis, and malaria during 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Global, regional, and national levels and causes of maternal mortality during 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Global, regional, and national levels of neonatal, infant, and under-5 mortality during 1990-2013: a systematic analysis for the Global Burden of Disease Study 2013.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Human recombinant lysozyme downregulates advanced glycation endproduct-induced interleukin-6 production and release in an in-vitro model of human proximal tubular epithelial cells.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Midline 1 directs lytic granule exocytosis and cytotoxicity of mouse killer T cells.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Molecular analysis of Fanconi anemia: the experience of the Bone Marrow Failure Study Group of the Italian Association of Pediatric Onco-Hematology.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">MYH9-related disease: a novel prognostic model to predict the clinical evolution of the disease based on genotype-phenotype correlations.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Salt-inducible kinase 3, SIK3, is a new gene associated with hearing.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Spectrum of the mutations in Bernard-Soulier syndrome.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Trans-ethnic meta-analysis of white blood cell phenotypes.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">MYH9-related disease: five novel mutations expanding the spectrum of causative mutations and confirming genotype/phenotype correlations.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Accuracy of diagnostic antibody tests for coeliac disease in children: summary of an evidence report.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Coeliac disease diagnosis: ESPGHAN 1990 criteria or need for a change? Results of a questionnaire.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">European Society for Pediatric Gastroenterology, Hepatology, and Nutrition guidelines for the diagnosis of coeliac disease.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Evidence of inbreeding depression on human height.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genome-wide association and functional follow-up reveals new loci for kidney function.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Haematopoietic SCT in severe autoimmune diseases: updated guidelines of the European Group for Blood and Marrow Transplantation.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">International collaboration as a tool for diagnosis of patients with inherited thrombocytopenia in the setting of a developing country.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Meta-analyses identify 13 loci associated with age at menopause and highlight DNA repair and immune pathways.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">The active Zot domain (aa 288-293) increases ZO-1 and myosin 1C serine/threonine phosphorylation, alters interaction between ZO-1 and its binding partners, and induces tight junction disassembly through proteinase activated receptor 2 activation.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">ESPGHAN's 2008 recommendation for early introduction of complementary foods: how good is the evidence?</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Forkhead box protein 3 (FOXP3) mutations lead to increased TH17 cell numbers and regulatory T-cell instability.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">"GINEXMAL RCT: Induction of labour versus expectant management in gestational diabetes pregnancies".</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathways.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">High incidence of NLRP3 somatic mosaicism in patients with chronic infantile neurologic, cutaneous, articular syndrome: results of an International Multicenter Collaborative Study.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Horizontal gaze palsy and progressive scoliosis without ROBO3 mutations.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Marriage and parenthood among childhood cancer survivors: a report from the Italian AIEOP Off-Therapy Registry.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Multiple loci are associated with white blood cell phenotypes.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Therapeutic approaches in the treatment of juvenile dermatomyositis in patients with recent-onset disease and in those experiencing disease flare: an international multicenter PRINTO study.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Abatacept improves health-related quality of life, pain, sleep quality, and daily participation in subjects with juvenile idiopathic arthritis.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Anti transglutaminase antibodies cause ataxia in mice.</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%">Development of paediatric quality of inpatient care indicators for low-income countries - A Delphi study.</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%">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%">MYH9-related disease: Report on five German families and description of a novel mutation.</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%">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%">Toward a consensus on guiding principles for health systems strengthening.</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>Drupal-Biblio17<style face="normal" font="default" size="100%">Atomic models for the polypeptide backbones of myohemerythrin and hemerythrin.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Effect of chloroquine on cultured fibroblasts: release of lysosomal hydrolases and inhibition of their uptake.</style>