BALSAMO, ANTONIO
BALSAMO, ANTONIO
DIPARTIMENTO DI SCIENZE MEDICHE E CHIRURGICHE
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.
46, XX DSD due to androgen excess in monogenic disorders of steroidogenesis: Genetic, biochemical, and clinical features
2019 Federico Baronio, Rita Ortolano, Soara Menabò, Alessandra Cassio, Lilia Baldazzi, Valeria Di Natale, Giacomo Tonti, Benedetta Vestrucci, Antonio Balsamo
A genetic epidemiology study of congenital adrenal hyperplasia in Italy
2018 Gialluisi, A; Menabò, S; Baldazzi, L; Casula, L; Meloni, A; Farci, M. C; Mariotti, S; Balestrino, L; Ortolano, R; Murru, S; Carcassi, C; Loche, S; Balsamo, A; Romeo, G.
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 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.
Alterazioni endocrino metaboliche nell’obesità dell’età evolutiva.
2011 A.Balsamo
Altri agenti farmacologici
2005 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 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 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.
Behavioural and emotional aspects in obese children.
2006 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 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 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 Bertelloni S, Meriggiola MC, Dati E, Balsamo A, Baroncelli GI
Changes over time in sex assignment for disorders of sex development
2014 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
| 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 | - |
| 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 Nata...le, 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 genetic epidemiology study of congenital adrenal hyperplasia in Italy | Gialluisi, A; Menabò, S; Baldazzi, L; Casula, L; Meloni, A; Farci, M. C; Mariotti, S; Balestrino,... L; Ortolano, R; Murru, S; Carcassi, C; Loche, S; Balsamo, A; Romeo, G. | 2018-01-01 | CLINICAL GENETICS | - | 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 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 | - |
| 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.M...odestini; 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; Rod...ie, 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 | - |