GENNARI, MONIA
GENNARI, MONIA
ARAG - AREA FINANZA E CONTABILITÀ
Collaboratori
Gennari M.; M. GENNARI
Measles virus and cytomegalovirus co-infection, in a child with recent SARS-CoV-2 infection, during COVID-19 pandemic: a case report
2023 Piccirilli, Giulia; Gennari, Monia; Gabrielli, Liliana; Leone, Marta; Borgatti, Eva Caterina; Cantiani, Alessia; Lanna, Federica; Magurano, Fabio; Baggieri, Melissa; Marangoni, Antonella; Lanari, Marcello; Lazzarotto, Tiziana
Visceral Leishmaniasis: Epidemiology, Diagnosis, and Treatment Regimens in Different Geographical Areas with a Focus on Pediatrics
2022 Scarpini S.; Dondi A.; Totaro C.; Biagi C.; Melchionda F.; Zama D.; Pierantoni L.; Gennari M.; Campagna C.; Prete A.; Lanari M.
Childhood medical history and psychosis in adult life: Findings from the Bologna EU-GEI incidence and case–control study
2021 D'Andrea G.; Suprani F.; Tolomelli E.; Gennari M.; Lanari M.; Faldella G.; Muratori R.; Berardi D.; Tarricone I.
Impact of guidelines publication on acute bronchiolitis management: 10-year experience from a tertiary care center in Italy
2021 Biagi C.; Scarpini S.; Paleari C.; Fabi M.; Dondi A.; Gabrielli L.; Gennari M.; Lanari M.; Pierantoni L.
When the Woman Is the Mother: The Work of Pediatrician for Caring Mothers and Children
2019 Lanari, Marcello; Gennari, Monia; Biagi, Carlotta
Gastrite erosiva da allergia alle proteine del latte vaccino: una patologia rara ma non troppo.
2018 Arianna Giannetti, Barbara Bendandi, Tommaso Gargano, Monia Gennari, Francesca Cipriani
Growing Up with Type 1 narcolepsy: Its anthropometric and endocrine features
2016 Ponziani, Virginia; Gennari, Monia; Pizza, Fabio; Balsamo, Antonio; Bernardi, Filippo; Plazzi, Giuseppe
Early corticosteroid treatment in 4 Duchenne muscular dystrophy patients: 14-years follow-up
2012 Merlini L; Gennari M; Malaspina E; Cecconi I; Armaroli A; Gnudi S; Talim B; Ferlini A; Cicognani A; Franzoni E
Insulin resistance is a risk factor for high blood pressure regardless of body size and fat distribution in obese children.
2010 Maffeis C; Banzato C; Brambilla P; Cerutti F; Corciulo N; Cuccarolo G; Di Pietro M; Franzese A; Gennari M; Balsamo A; Grugni G; Iughetti L; Del Giudice EM; Petri A; Trada M; Yiannakou P; Obesity Study Group of the Italian Society of Pediatric Endocrinology and Diabetology
Characterization of deletions at 9p affecting the candidate regions for sex reversal and deletion 9p syndrome by MLPA.
2009 Barbaro M.; Balsamo A.; Anderlid B.M.; Myhre A.G.; Gennari M.; Nicoletti A.; Pittalis M.C.; Oscarson M.; Wedell A.
Obesità essenziale: diagnosi
2009 Gennari M.; Balsamo A.
A novel PRKAR1A mutation associated with hepatocellular carcinoma in a young patient and a variable Carney complex phenotype in affected subjects in older generations.
2008 Gennari M; Stratakis CA; Hovarth A; Pirazzoli P; Cicognani A.
Three new mutations in androgen receptor gene identified in patients with 46,XY SDS: Complications for genetic counselling
2008 Nicoletti A.; Baldazzi L.; Menabò S.; Gennari M.; Cangemi G.; Maccaferri M.; Cicognani A.
Three Novel AMHGene Mutations in a Patient with Persistent Mullerian Duct Syndrome and Normal AMH Serum Dosage.
2008 Menabò S; Balsamo A; Nicoletti A; Gennari M; Pirazzoli P; Cicognani A; Baldazzi L.
A molecular analysis of candidate genes for hypospadias in Italian subjects
2007 Nicoletti A.; Baldazzi L.; Menabò S.; Balsamo A.; Gennari M.; Buzi F.; Pasini A.; Cicognani A.
A new case of familial mutation in the SRY gene implicated in the pure gonadal dysgenesis in two sisters and in their unaffected father
2007 P. Pirazzoli; A. Nicoletti; M. Gennari; L. Baldazzi; A. Balsamo; F. Mencarelli; A. Cicognani
A new case of familial mutation in the SRY gene implicated in the pure gonadal dysgenesis in two sisters and their unaffected father
2007 Pirazzoli P.; Nicoletti A.; Gennari M.; Baldazzi L.; Balsamo A.; Mencarelli F.; Cicognani A.
Autosomal dominant pseudohypoaldosteronism type 1 (PHA1) in the Italian population: functional characterization of two novel hMR (NR3C2) gene mutations and frequency and function of three gene SNPs
2007 Balsamo A.; Cicognani A.; Gennari M.; Sippel W.G.; Menabò S.; Baronio F.; Riepe F.
Functional characterization of naturally occurring NR3C2 gene mutations in Italian patients suffering from pseudohypoaldosteronism type 1
2007 A.Balsamo; A.Cicognani; M.Gennari; W.G.Sippell; S.Menabò; F.Baronio; F.G.Riepe
Melanocortin-4-receptor molecular screening in a group of phenotypically selected obese children: report of two new mutations and lack of association to the early onset of the disease
2007 Santoro N.; Cirillo G.; Romano T.; ..; Balsamo A.; Gennari M.; ..; Miraglia del Giudice E.