GENNARI, MONIA
GENNARI, MONIA
Gennari M.; M. GENNARI
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.
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.
Active and total ghrelin concentrations in the newborn
2005 Pirazzoli P; Lanari M; Zucchini S; Gennari M; Pagotto U; De Iasio R; Pasquali R; Cassio A; Cicognani A; Cacciari E.
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.
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.
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.
Due casi falsi negativi con forma classica allo screening neonatale per la sindrome adreno-genitale congenita della Regione Emilia-Romagna (1980-83, 1991-2003).
2004 A.Balsamo; S.Piazzi; M.Bal; C.Retetangos; M.Gennari; F.Baronio; A.Cassio; A.Cicognani.
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
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
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
Gonadal dysgenesis and XY sex reversal in one patient with a deletion of the distal short arm of chromosome 9 (9p).
2004 A.Balsamo; M.Gennari; MC.Pittalis; P.Biso; L.Baldazzi; L.Mazzanti; R.De Castro; A.Cicognani.
Growing Up with Type 1 narcolepsy: Its anthropometric and endocrine features
2016 Ponziani, Virginia; Gennari, Monia; Pizza, Fabio; Balsamo, Antonio; Bernardi, Filippo; Plazzi, Giuseppe
Height outcome and pubertal development in CYP21 genotyped CAH male patients
2004 A.Balsamo; L.Baldazzi; L.Barp; F.Baronio; M.Gennari; C.Retetangos; A.Cassio; A.Cicognani; E.Cacciari.
High Variability of Sexual Ambiguity and Clinical Expression in two Patients with a 46,XY del(9p) Kariotype
2004 A. Balsamo; M. Gennari; E. Malpezzi; A. Mattarozzi; S. Strocchi; A. L. Nicoletti; A. Cicognani; E. Cacciari
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.
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
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.
Metabolic Aspects of Patients Followed for Severe Obesity
2004 M. Gennari; A. Balsamo; M. Bal; L. Baldazzi; S. Gualandi; F. Mencarelli; I. Bettocchi; A. Cicognani; E. Cacciari
Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
---|---|---|---|---|---|---|
A molecular analysis of candidate genes for hypospadias in Italian subjects | Nicoletti A.; Baldazzi L.; Menabò S.; Balsamo A.; Gennari M.; Buzi F.; Pasini A.; Cicognani A. | 2007-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
A new case of familial mutation in the SRY gene implicated in the pure gonadal dysgenesis in two sisters and in their unaffected father |
P. Pirazzoli; A. Nicoletti; M. Gennari; L. Baldazzi; A. Balsamo; F. Mencarelli; A. Cicognani |
2007-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
A new case of familial mutation in the SRY gene implicated in the pure gonadal dysgenesis in two sisters and their unaffected father | Pirazzoli P.; Nicoletti A.; Gennari M.; Baldazzi L.; Balsamo A.; Mencarelli F.; Cicognani A. | 2007-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
A novel PRKAR1A mutation associated with hepatocellular carcinoma in a young patient and a variable Carney complex phenotype in affected subjects in older generations. | Gennari M; Stratakis CA; Hovarth A; Pirazzoli P; Cicognani A. | 2008-01-01 | CLINICAL ENDOCRINOLOGY | - | 1.01 Articolo in rivista | - |
Active and total ghrelin concentrations in the newborn | Pirazzoli P; Lanari M; Zucchini S; Gennari M; Pagotto U; De Iasio R; Pasquali R; Cassio A; Cicogn...ani A; Cacciari E. | 2005-01-01 | JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM | - | 1.01 Articolo in rivista | - |
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 | Balsamo A.; Cicognani A.; Gennari M.; Sippel W.G.; Menabò S.; Baronio F.; Riepe F. | 2007-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
Characterization of deletions at 9p affecting the candidate regions for sex reversal and deletion 9p syndrome by MLPA. |
Barbaro M.; Balsamo A.; Anderlid B.M.; Myhre A.G.; Gennari M.; Nicoletti A.; Pittalis M.C.; Osca...rson M.; Wedell A. |
2009-01-01 | EUROPEAN JOURNAL OF HUMAN GENETICS | - | 1.01 Articolo in rivista | - |
Childhood medical history and psychosis in adult life: Findings from the Bologna EU-GEI incidence and case–control study | D'Andrea G.; Suprani F.; Tolomelli E.; Gennari M.; Lanari M.; Faldella G.; Muratori R.; Berardi D....; Tarricone I. | 2021-01-01 | EARLY INTERVENTION IN PSYCHIATRY | - | 1.01 Articolo in rivista | Chidhood_preprint.pdf |
Due casi falsi negativi con forma classica allo screening neonatale per la sindrome adreno-genitale congenita della Regione Emilia-Romagna (1980-83, 1991-2003). | A.Balsamo; S.Piazzi; M.Bal; C.Retetangos; M.Gennari; F.Baronio; A.Cassio; A.Cicognani. | 2004-01-01 | - | n.s. | 4.02 Riassunto (Abstract) | - |
Early corticosteroid treatment in 4 Duchenne muscular dystrophy patients: 14-years follow-up | Merlini L; Gennari M; Malaspina E; Cecconi I; Armaroli A; Gnudi S; Talim B; Ferlini A; Cicognani ...A; Franzoni E | 2012-01-01 | MUSCLE & NERVE | - | 1.01 Articolo in rivista | - |
Functional characterization of naturally occurring NR3C2 gene mutations in Italian patients suffering from pseudohypoaldosteronism type 1 | A.Balsamo; A.Cicognani; M.Gennari; W.G.Sippell; S.Menabò; F.Baronio; F.G.Riepe | 2007-01-01 | EUROPEAN JOURNAL OF ENDOCRINOLOGY | - | 1.01 Articolo in rivista | - |
Gastrite erosiva da allergia alle proteine del latte vaccino: una patologia rara ma non troppo. | Arianna Giannetti, Barbara Bendandi, Tommaso Gargano, Monia Gennari, Francesca Cipriani | 2018-01-01 | RIVISTA DI IMMUNOLOGIA E ALLERGOLOGIA PEDIATRICA | - | 1.01 Articolo in rivista | - |
Gonadal dysgenesis and XY sex reversal in one patient with a deletion of the distal short arm of chromosome 9 (9p). | A.Balsamo; M.Gennari; MC.Pittalis; P.Biso; L.Baldazzi; L.Mazzanti; R.De Castro; A.Cicognani. | 2004-01-01 | - | O.Hiort | 4.02 Riassunto (Abstract) | - |
Growing Up with Type 1 narcolepsy: Its anthropometric and endocrine features | Ponziani, Virginia; Gennari, Monia; Pizza, Fabio; Balsamo, Antonio; Bernardi, Filippo; Plazzi, Gi...useppe | 2016-01-01 | JOURNAL OF CLINICAL SLEEP MEDICINE | - | 1.01 Articolo in rivista | - |
Height outcome and pubertal development in CYP21 genotyped CAH male patients | A.Balsamo; L.Baldazzi; L.Barp; F.Baronio; M.Gennari; C.Retetangos; A.Cassio; A.Cicognani; E.Cacci...ari. | 2004-01-01 | - | s.n | 4.02 Riassunto (Abstract) | - |
High Variability of Sexual Ambiguity and Clinical Expression in two Patients with a 46,XY del(9p) Kariotype |
A. Balsamo; M. Gennari; E. Malpezzi; A. Mattarozzi; S. Strocchi; A. L. Nicoletti; A. Cicognani; ...E. Cacciari |
2004-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
Impact of guidelines publication on acute bronchiolitis management: 10-year experience from a tertiary care center in Italy | Biagi C.; Scarpini S.; Paleari C.; Fabi M.; Dondi A.; Gabrielli L.; Gennari M.; Lanari M.; Pieran...toni L. | 2021-01-01 | MICROORGANISMS | - | 1.01 Articolo in rivista | microorganisms-09-02221.pdf |
Insulin resistance is a risk factor for high blood pressure regardless of body size and fat distribution in obese children. | Maffeis C; Banzato C; Brambilla P; Cerutti F; Corciulo N; Cuccarolo G; Di Pietro M; Franzese A; G...ennari 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 | 2010-01-01 | NMCD. NUTRITION METABOLISM AND CARDIOVASCULAR DISEASES | - | 1.01 Articolo in rivista | - |
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 | Santoro N.; Cirillo G.; Romano T.; ..; Balsamo A.; Gennari M.; ..; Miraglia del Giudice E. | 2007-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
Metabolic Aspects of Patients Followed for Severe Obesity |
M. Gennari; A. Balsamo; M. Bal; L. Baldazzi; S. Gualandi; F. Mencarelli; I. Bettocchi; A. Cicogn...ani; E. Cacciari |
2004-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |