CICOGNANI, ALESSANDRO

CICOGNANI, ALESSANDRO  

DIPARTIMENTO DI SCIENZE GINECOLOGICHE, OSTETRICHE E PEDIATRICHE  

CICOGNANI A.; A. CICOGNANI; Alessandro Cicognani  

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Risultati 1 - 20 di 126 (tempo di esecuzione: 0.027 secondi).
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) -