BALSAMO, ANTONIO
BALSAMO, ANTONIO
DIPARTIMENTO DI SCIENZE MEDICHE E CHIRURGICHE
17beta-Hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescence
2009-01-01 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.
46, XX DSD due to androgen excess in monogenic disorders of steroidogenesis: Genetic, biochemical, and clinical features
2019-01-01 Federico Baronio, Rita Ortolano, Soara Menabò, Alessandra Cassio, Lilia Baldazzi, Valeria Di Natale, Giacomo Tonti, Benedetta Vestrucci, Antonio Balsamo
A molecular analysis of candidate genes for hypospadias in Italian subjects
2007-01-01 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
2007-01-01 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
2007-01-01 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
2007-01-01 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
2005-01-01 Balsamo A.; Antelli A.; Baldazzi L.; Baronio F.; Lazareva D.; Cassio A.; Cicognani A.
Alterazioni endocrino metaboliche nell’obesità dell’età evolutiva.
2011-01-01 A.Balsamo
Altri agenti farmacologici
2005-01-01 Gennari M.; Balsamo A.; Cicognani A.
Analisi dei geni dell’asse melanocortinico in bambini con obesità ad esordio precoce: risultati preliminari di uno studio multicentrico.
2005-01-01 E.Miraglia Del Giudice; G.Cirillo; G.Morino; L.Iughetti; A.Vottero; A.Salvatoni; M.Di Pietro; E.Modestini; A.Balsamo; M.Gennari; L.Perrone.
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
2007-01-01 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
2007-01-01 Balsamo A.; Cicognani A.; Gennari M.; Sippel W.G.; Menabò S.; Baronio F.; Riepe F.
Behavioural and emotional aspects in obese children.
2006-01-01 N.Bisacchi; L.Nardi; M.Gennari; A.Balsamo; D.Gaddoni; C.Giovannini; F.D’Alberton; A.Cicognani.
Birth length and weight in congenital adrenal hyperplasia according to the different phenotypes.
2006-01-01 Balsamo A.; Wasniewska M.; Di Pasquale G.; Salzano G.; Baronio F.; Bombaci S.; De Luca F.
Birth length and weight in congenital adrenal hyperplasia according to the different phenotype.
2006-01-01 A.Balsamo; M.Wasniewska; G.Di Pasquale; G.Salzano; G.Zirilli; F.Baronio; M.Valenzise; F.De Luca.
Bone Mineral Density in Women Living with Complete Androgen Insensitivity Syndrome and Intact Testes or Removed Gonads.
2017-01-01 Bertelloni S, Meriggiola MC, Dati E, Balsamo A, Baroncelli GI
Changes over time in sex assignment for disorders of sex development
2014-01-01 Kolesinska, Zofia; Ahmed, S. Faisal; Niedziela, Marek; Bryce, Jillian; Molinska-Glura, Marta; Rodie, Martina; Jiang, Jipu; Sinnott, Richard O.; Hughes, Ieuan A.; Darendeliler, Feyza; Hiort, Olaf; Van Der Zwan, Yvonne; Cools, Martine; Guran, Tulay; Holterhus, Paul-Martin; Bertelloni, Silvano; Lisa, Lidka; Arlt, Wiebke; Krone, Nils; Ellaithi, Mona; Balsamo, Antonio; Mazen, Inas; Nordenstrom, Anna; Lachlan, Katherine; Alkhawari, Mona; Chatelain, Pierre; Weintrob, Naomi
Characterization of deletions at 9p affecting the candidate regions for sex reversal and deletion 9p syndrome by MLPA.
2009-01-01 Barbaro M.; Balsamo A.; Anderlid B.M.; Myhre A.G.; Gennari M.; Nicoletti A.; Pittalis M.C.; Oscarson M.; Wedell A.
Clinical Management of CAH
2006-01-01 A.Balsamo
Comment on "complete androgen insensitivity syndrome: optimizing diagnosis and management"
2014-01-01 Balsamo, Antonio; Baronio, Federico; Berra, Marta; Bertelloni, Silvano; D'Alberton, Franco; Marrocco, Giacinto; Vallasciani, Santiago
| 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.; Nicoletti 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 | - |
| 46, XX DSD due to androgen excess in monogenic disorders of steroidogenesis: Genetic, biochemical, and clinical features | Federico Baronio, Rita Ortolano, Soara Menabò, Alessandra Cassio, Lilia Baldazzi, Valeria Di Natale, Giacomo Tonti, Benedetta Vestrucci, Antonio Balsamo | 2019-01-01 | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | - | 1.01 Articolo in rivista | 46,XX DSD.pdf; ijms-20-04605-s001.pdf |
| A molecular analysis of candidate genes for hypospadias in Italian subjects | Annalisa Nicoletti; Lilia Baldazzi; Soara Menabò; Antonio Balsamo; Monia Gennari; Fabio Buzi; Andrea 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 | - |
| Alterazioni endocrino metaboliche nell’obesità dell’età evolutiva. | A.Balsamo | 2011-01-01 | - | Meeteng Planner SRL | 2.01 Capitolo / saggio in libro | - |
| Altri agenti farmacologici | Gennari M.; Balsamo A.; Cicognani A. | 2005-01-01 | - | McGraw-Hill Editor, Publishing Group Italia | 2.01 Capitolo / saggio in libro | - |
| Analisi dei geni dell’asse melanocortinico in bambini con obesità ad esordio precoce: risultati preliminari di uno studio multicentrico. | E.Miraglia Del Giudice; G.Cirillo; G.Morino; L.Iughetti; A.Vottero; A.Salvatoni; M.Di Pietro; E.Modestini; A.Balsamo; M.Gennari; L.Perrone. | 2005-01-01 | - | R.Saggiorato & C. s.a.s. | 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) | - |
| Behavioural and emotional aspects in obese children. | N.Bisacchi; L.Nardi; M.Gennari; A.Balsamo; D.Gaddoni; C.Giovannini; F.D’Alberton; A.Cicognani. | 2006-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
| Birth length and weight in congenital adrenal hyperplasia according to the different phenotypes. | Balsamo A.; Wasniewska M.; Di Pasquale G.; Salzano G.; Baronio F.; Bombaci S.; De Luca F. | 2006-01-01 | EUROPEAN JOURNAL OF PEDIATRICS | - | 1.01 Articolo in rivista | - |
| Birth length and weight in congenital adrenal hyperplasia according to the different phenotype. | A.Balsamo; M.Wasniewska; G.Di Pasquale; G.Salzano; G.Zirilli; F.Baronio; M.Valenzise; F.De Luca. | 2006-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
| Bone Mineral Density in Women Living with Complete Androgen Insensitivity Syndrome and Intact Testes or Removed Gonads. | Bertelloni S, Meriggiola MC, Dati E, Balsamo A, Baroncelli GI | 2017-01-01 | SEXUAL DEVELOPMENT | - | 1.01 Articolo in rivista | - |
| Changes over time in sex assignment for disorders of sex development | Kolesinska, Zofia; Ahmed, S. Faisal; Niedziela, Marek; Bryce, Jillian; Molinska-Glura, Marta; Rodie, Martina; Jiang, Jipu; Sinnott, Richard O.; Hughes, Ieuan A.; Darendeliler, Feyza; Hiort, Olaf; Van Der Zwan, Yvonne; Cools, Martine; Guran, Tulay; Holterhus, Paul-Martin; Bertelloni, Silvano; Lisa, Lidka; Arlt, Wiebke; Krone, Nils; Ellaithi, Mona; Balsamo, Antonio; Mazen, Inas; Nordenstrom, Anna; Lachlan, Katherine; Alkhawari, Mona; Chatelain, Pierre; Weintrob, Naomi | 2014-01-01 | PEDIATRICS | - | 1.01 Articolo in rivista | - |
| 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.; Oscarson M.; Wedell A. | 2009-01-01 | EUROPEAN JOURNAL OF HUMAN GENETICS | - | 1.01 Articolo in rivista | - |
| Clinical Management of CAH | A.Balsamo | 2006-01-01 | - | s.n | 4.01 Contributo in Atti di convegno | - |
| Comment on "complete androgen insensitivity syndrome: optimizing diagnosis and management" | Balsamo, Antonio; Baronio, Federico; Berra, Marta; Bertelloni, Silvano; D'Alberton, Franco; Marrocco, Giacinto; Vallasciani, Santiago | 2014-01-01 | CASE REPORTS IN OBSTETRICS AND GYNECOLOGY | - | 1.04 Replica / breve intervento (e simili) | - |