CICOGNANI, ALESSANDRO
CICOGNANI, ALESSANDRO
DIPARTIMENTO DI SCIENZE GINECOLOGICHE, OSTETRICHE E PEDIATRICHE
CICOGNANI A.; A. CICOGNANI; Alessandro Cicognani
17beta-Hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescence
2009 Bertelloni S.; Balsamo A.; Giordani L. ; Fischetto R.; Russo G.; Delvecchio M.; Gennari M.; Nicoletti A.; Maggio M.C.; Concolino D.; Cavallo L.; Cicognani A.; Chiumello G.; Hiort O.; Baroncelli G.I.; Faienza M.F.
A molecular analysis of candidate genes for hypospadias in Italian subjects
2007 Annalisa Nicoletti; Lilia Baldazzi; Soara Menabò; Antonio Balsamo; Monia Gennari; Fabio Buzi; Andrea Pasini; Alessandro Cicognani
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 new DAX1 gene mutation associated with congenital adrenal hypoplasia and hypogonadotropic hypogonadism
2005 Balsamo A.; Antelli A.; Baldazzi L.; Baronio F.; Lazareva D.; Cassio A.; Cicognani A.
A novel frame-shift mutation in the SHOX gene in a subject with Léri-Weill dyschondrosteosis
2005 Nicoletti A.; Baldazzi L.; Antelli A.; Mazzanti L.; Baronio F.; Menabò S.; Pirazzoli P.; 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.
A rare association of inlet patch with laryngospasm: a report of two children and literature review.
2011 E. di Palmo;S. Cazzato;S. Tursini;N.C.M Salfi;A. Mazzotta;C. Di Silverio Carulli;M. Lima;R. Bergamaschi;F. Bernardi;A. Cicognani
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of Congenital Adrenal Hyperplasia
2010 S. Menabo;A.Balsamo; L. Baldazzi; M. Barbaro; A. Nicoletti; V.Conti; P. Pirazzoli; A. Wedell; A. Cicognani
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of congenital adrenal hyperplasia.
2012 Menabò S; Balsamo A; Baldazzi L; Barbaro M; Nicoletti A; Conti V; Pirazzoli P; Wedell A; Cicognani A.
Acanthosis Nigricans (AN), Glucose Tolerance and Turner Syndrome: Influence of GH-Therapy
2004 R. Bergamaschi; L. Mazzanti; E. Scarano; I. Neri; S. Strocchi; V. Rosetti; L. Castiglioni; F. Zappulla; A. Cicognani; E. Cacciari
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.
Age at onset do not influence long-term glycemic control in children with type 1 diabetes mellitus
2005 S. Salardi;S. Zucchini;R. Santoni;D. Elleri;M. Scipione;I. Bettocchi;S. Gualandi;A. Cicognani
Airway inflammation and lung function decline in childhood post-infectious bronchiolitis obliterans.
2008 Cazzato S; Poletti V; Bernardi F; Loroni L; Bertelli L; Colonna S; Zappulla F; Timoncini G; Cicognani A.
Altri agenti farmacologici
2005 Gennari M.; Balsamo A.; Cicognani A.
Analysis of the TSHR gene in patients with isolated hyperthyrotropinemia
2005 M. Bal;L. Barp;A. Cassio;L. Baldazzi;S. Salardi;L. Lugaresi;A. Cicognani
AutoimmunePolyendocrinopathyCandidiasisEctodermalDystrophy Syndrome(APECED) clinical and molecular features in three patients from southernItaly.
2008 F.Baronio;A Cassio; G.Tonini; E.Faleschini; M.Gallucci; C.Betterle; ; A .Cicognani
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 NR3C2 gene SNPs
2007 Antonio Balsamo; Alessandro Cicognani; Monia Gennari; Wolfgang G Sippel; Soara Menabò; Federico Baronio; Wolfgang G Riepe
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.
Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
---|---|---|---|---|---|---|
17beta-Hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescence | Bertelloni S.; Balsamo A.; Giordani L. ; Fischetto R.; Russo G.; Delvecchio M.; Gennari M.; Nicol...etti A.; Maggio M.C.; Concolino D.; Cavallo L.; Cicognani A.; Chiumello G.; Hiort O.; Baroncelli G.I.; Faienza M.F. | 2009-01-01 | JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION | - | 1.01 Articolo in rivista | - |
A molecular analysis of candidate genes for hypospadias in Italian subjects |
Annalisa Nicoletti; Lilia Baldazzi; Soara Menabò; Antonio Balsamo; Monia Gennari; Fabio Buzi; An...drea Pasini; Alessandro Cicognani |
2007-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
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 new DAX1 gene mutation associated with congenital adrenal hypoplasia and hypogonadotropic hypogonadism | Balsamo A.; Antelli A.; Baldazzi L.; Baronio F.; Lazareva D.; Cassio A.; Cicognani A. | 2005-01-01 | AMERICAN JOURNAL OF MEDICAL GENETICS. PART A | - | 1.01 Articolo in rivista | - |
A novel frame-shift mutation in the SHOX gene in a subject with Léri-Weill dyschondrosteosis | Nicoletti A.; Baldazzi L.; Antelli A.; Mazzanti L.; Baronio F.; Menabò S.; Pirazzoli P.; Cicognan...i A. | 2005-01-01 | 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 | - |
A rare association of inlet patch with laryngospasm: a report of two children and literature review. | E. di Palmo;S. Cazzato;S. Tursini;N.C.M Salfi;A. Mazzotta;C. Di Silverio Carulli;M. Lima;R. Berga...maschi;F. Bernardi;A. Cicognani | 2011-01-01 | PEDIATRIC PULMONOLOGY | - | 1.01 Articolo in rivista | - |
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of Congenital Adrenal Hyperplasia | S. Menabo;A.Balsamo; L. Baldazzi; M. Barbaro; A. Nicoletti; V.Conti; P. Pirazzoli; A. Wedell; A. ...Cicognani | 2010-01-01 | HORMONE RESEARCH IN PAEDIATRICS | - | 4.02 Riassunto (Abstract) | - |
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of congenital adrenal hyperplasia. | Menabò S; Balsamo A; Baldazzi L; Barbaro M; Nicoletti A; Conti V; Pirazzoli P; Wedell A; Cicognan...i A. | 2012-01-01 | JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION | - | 1.01 Articolo in rivista | - |
Acanthosis Nigricans (AN), Glucose Tolerance and Turner Syndrome: Influence of GH-Therapy |
R. Bergamaschi; L. Mazzanti; E. Scarano; I. Neri; S. Strocchi; V. Rosetti; L. Castiglioni; F. Za...ppulla; A. Cicognani; E. Cacciari |
2004-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
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 | - |
Age at onset do not influence long-term glycemic control in children with type 1 diabetes mellitus | S. Salardi;S. Zucchini;R. Santoni;D. Elleri;M. Scipione;I. Bettocchi;S. Gualandi;A. Cicognani | 2005-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
Airway inflammation and lung function decline in childhood post-infectious bronchiolitis obliterans. | Cazzato S; Poletti V; Bernardi F; Loroni L; Bertelli L; Colonna S; Zappulla F; Timoncini G; Cicog...nani A. | 2008-01-01 | PEDIATRIC PULMONOLOGY | - | 1.01 Articolo in rivista | - |
Altri agenti farmacologici | Gennari M.; Balsamo A.; Cicognani A. | 2005-01-01 | - | McGraw-Hill Editor, Publishing Group Italia | 2.01 Capitolo / saggio in libro | - |
Analysis of the TSHR gene in patients with isolated hyperthyrotropinemia | M. Bal;L. Barp;A. Cassio;L. Baldazzi;S. Salardi;L. Lugaresi;A. Cicognani | 2005-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
AutoimmunePolyendocrinopathyCandidiasisEctodermalDystrophy Syndrome(APECED) clinical and molecular features in three patients from southernItaly. | F.Baronio;A Cassio; G.Tonini; E.Faleschini; M.Gallucci; C.Betterle; ; A .Cicognani | 2008-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
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 NR3C2 gene SNPs |
Antonio Balsamo; Alessandro Cicognani; Monia Gennari; Wolfgang G Sippel; Soara Menabò; Federico ...Baronio; Wolfgang G Riepe |
2007-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
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) | - |