CICOGNANI, ALESSANDRO
CICOGNANI, ALESSANDRO
DIPARTIMENTO DI SCIENZE GINECOLOGICHE, OSTETRICHE E PEDIATRICHE
CICOGNANI A.; A. CICOGNANI; Alessandro Cicognani
Increased large artery intima media thickness in adolescents with either classical or non-classical congenital adrenal hyperplasia
2013 M. Wasniewska; A. Balsamo; M. Valenzise; A. Manganaro; G. Faggioli; S. Bombaci; V. Conti; M. Ferri; T. Aversa; A. Cicognani; F. De Luca
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.
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
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
Disorders of sexual development
2011 Balsamo, Antonio; Cicognani, Alessandro; Ghirri, P.; Scaramuzzo, R. T.; D’Alberton, F.; Bertelloni, S.; Boldrini, A.
Hashimoto encepahlopathy in an adolescent boy.
2011 A.Cassio; M. Gallucci; D.Tassinari; S.Monti;A.Rizzello; MO.Bal;A.Cicognani
Hearing Growth Defects in Turner Syndrome
2011 R. Bergamaschi; C. Bergonzoni; L. Mazzanti; E. Scarano; F. Mencarelli; V. Rosetti; F. Messina; L. Iughetti; A. Cicognani
High Rate of Regression From Micro-Macroalbuminuria to Normoalbuminuria in Children and Adolescents With Type 1 Diabetes Treated or Not With Enalapril: The influence of HDL cholesterol
2011 S. Salardi;C. Balsamo;S. Zucchini;G. Maltoni;M. Scipione;A. Rollo;S. Gualandi;A. Cicognani
psychological and behavioural aspects in children and adolescents with congenital hypothyroidism diagnosed by neonatal screening:comparison between parents' and children's perceptions
2011 N.Bisacchi; M.O.Bal;L.Nardi;I.Bettocchi;G.D'Addabbo;V.Conti; S.Monti;F.D'Alberton;A.Cicognani;A.Cassio
Study of the NR5A1 gene in a cohort of Italian patients with 46,XY Disorders of Sex Development (DSD) without adrenal insufficiency: identification of 7 novel mutations.
2011 Baldazzi, Lilia; Balsamo, Antonio; Nicoletti, Annalisa; Menabo', Soara; Rinaldini, D.; Cangemi, GIUSEPPE ALESSANDRO; Balsamo, Claudia; Pirazzoli, Piero; Cicognani, Alessandro
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of Congenital Adrenal Hyperplasia
2010 Menabo', Soara; Balsamo, Antonio; Baldazzi, Lilia; Barbaro, M.; Nicoletti, Annalisa; Conti, Veronica; Pirazzoli, Piero; Wedell, A.; Cicognani, Alessandro
HESX1 gene analysis in a population of 45 patients with posterior pituitari ectopia (PPE) and GH deficiency (GHD): two novel mutations associated with a mild phenotype.
2010 Baldazzi L.; Zucchini S.; Menabò S.; Nicoletti A.; Baronio F.; Cangemi G; Pirazzoli P.; Cicognani A.
Impact of molecular genetics on congenital adrenal hyperplasia management.
2010 A.Balsamo; L.Baldazzi; S.Menabò; A. Cicognani
Long-term clinical significance of thyroid autoimmunity in children with celiac disease.
2010 Cassio A.; Ricci G.; Baronio F.; Miniaci A.; Bal M.; Bigucci B.; Conti V.; Cicognani A.
The SHOX gene: a new indication for GH treatment
2010 Cicognani A.; Pirazzoli P.; Nicoletti A.; Baronio F.; Conti V.; Bonetti S.
Update on age at menarche in Italy: toward the leveling off of the secular trend.
2010 Rigon F.; Bianchin L.; Bernasconi S.; Bona G.; Bozzola M.; Buzi F.; Cicognani A.; De Sanctis C.; De Sanctis V.; Radetti G.; Tatò L.; Tonini G.; Perissinotto E.
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.
Correlations of phenotype and genotype in relation to mor phologic remodelling of the aortic root in patients with Turner's syndrome
2009 Prandstraller D; Mazzanti L; Giardini A; Lovato L; Tamburrino F; Scarano E; Cicognani A; Fattori R; Picchio FM
DEVELOPMENTAL SYNDROMES: GROWTH HORMONE DEFICIENCY AND TREATMENT.
2009 Mazzanti, L; Tamburrino, F; Bergamaschi, R; Scarano, E; Montanari, F; Torella, M; Ballarini, E; Cicognani, A.
Reproductive outcome in girls with congenital and acquired autoimmune thyroid pathology
2009 Cassio, Alessandra; Bal, MILVA ORQUIDEA; S., Sansavini; E., Ballarini; F., Parata; Bettocchi, Ilaria; Cicognani, Alessandro
| Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
|---|---|---|---|---|---|---|
| Increased large artery intima media thickness in adolescents with either classical or non-classical congenital adrenal hyperplasia | M. Wasniewska; A. Balsamo; M. Valenzise; A. Manganaro; G. Faggioli; S. Bombaci; V. Conti; M. Ferr...i; T. Aversa; A. Cicognani; F. De Luca | 2013-01-01 | JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION | - | 1.01 Articolo in rivista | - |
| 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 | - |
| 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 | - |
| 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 | - |
| Disorders of sexual development | Balsamo, Antonio; Cicognani, Alessandro; Ghirri, P.; Scaramuzzo, R. T.; D’Alberton, F.; Bertellon...i, S.; Boldrini, A. | 2011-01-01 | - | Springer Verlag | 2.01 Capitolo / saggio in libro | - |
| Hashimoto encepahlopathy in an adolescent boy. | A.Cassio; M. Gallucci; D.Tassinari; S.Monti;A.Rizzello; MO.Bal;A.Cicognani | 2011-01-01 | HORMONE RESEARCH IN PAEDIATRICS | - | 4.02 Riassunto (Abstract) | - |
| Hearing Growth Defects in Turner Syndrome | R. Bergamaschi; C. Bergonzoni; L. Mazzanti; E. Scarano; F. Mencarelli; V. Rosetti; F. Messina; L.... Iughetti; A. Cicognani | 2011-01-01 | - | V.R. Preedy, SPRINGER-VERLAG NEW YORK Inc., United States | 3.01 Monografia / trattato scientifico in forma di libro | - |
| High Rate of Regression From Micro-Macroalbuminuria to Normoalbuminuria in Children and Adolescents With Type 1 Diabetes Treated or Not With Enalapril: The influence of HDL cholesterol | S. Salardi;C. Balsamo;S. Zucchini;G. Maltoni;M. Scipione;A. Rollo;S. Gualandi;A. Cicognani | 2011-01-01 | DIABETES CARE | - | 1.01 Articolo in rivista | - |
| psychological and behavioural aspects in children and adolescents with congenital hypothyroidism diagnosed by neonatal screening:comparison between parents' and children's perceptions | N.Bisacchi; M.O.Bal;L.Nardi;I.Bettocchi;G.D'Addabbo;V.Conti; S.Monti;F.D'Alberton;A.Cicognani;A.C...assio | 2011-01-01 | EUROPEAN JOURNAL OF ENDOCRINOLOGY | - | 1.01 Articolo in rivista | - |
| Study of the NR5A1 gene in a cohort of Italian patients with 46,XY Disorders of Sex Development (DSD) without adrenal insufficiency: identification of 7 novel mutations. | Baldazzi, Lilia; Balsamo, Antonio; Nicoletti, Annalisa; Menabo', Soara; Rinaldini, D.; Cangemi, G...IUSEPPE ALESSANDRO; Balsamo, Claudia; Pirazzoli, Piero; Cicognani, Alessandro | 2011-01-01 | 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 | Menabo', Soara; Balsamo, Antonio; Baldazzi, Lilia; Barbaro, M.; Nicoletti, Annalisa; Conti, Veron...ica; Pirazzoli, Piero; Wedell, A.; Cicognani, Alessandro | 2010-01-01 | HORMONE RESEARCH IN PAEDIATRICS | - | 4.02 Riassunto (Abstract) | - |
| HESX1 gene analysis in a population of 45 patients with posterior pituitari ectopia (PPE) and GH deficiency (GHD): two novel mutations associated with a mild phenotype. | Baldazzi L.; Zucchini S.; Menabò S.; Nicoletti A.; Baronio F.; Cangemi G; Pirazzoli P.; Cicognani A. | 2010-01-01 | HORMONE RESEARCH IN PAEDIATRICS | - | 4.02 Riassunto (Abstract) | - |
| Impact of molecular genetics on congenital adrenal hyperplasia management. | A.Balsamo; L.Baldazzi; S.Menabò; A. Cicognani | 2010-01-01 | SEXUAL DEVELOPMENT | - | 1.01 Articolo in rivista | - |
| Long-term clinical significance of thyroid autoimmunity in children with celiac disease. | Cassio A.; Ricci G.; Baronio F.; Miniaci A.; Bal M.; Bigucci B.; Conti V.; Cicognani A. | 2010-01-01 | THE JOURNAL OF PEDIATRICS | - | 1.01 Articolo in rivista | - |
| The SHOX gene: a new indication for GH treatment | Cicognani A.; Pirazzoli P.; Nicoletti A.; Baronio F.; Conti V.; Bonetti S. | 2010-01-01 | JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION | - | 1.01 Articolo in rivista | - |
| Update on age at menarche in Italy: toward the leveling off of the secular trend. | Rigon F.; Bianchin L.; Bernasconi S.; Bona G.; Bozzola M.; Buzi F.; Cicognani A.; De Sanctis C.; ...De Sanctis V.; Radetti G.; Tatò L.; Tonini G.; Perissinotto E. | 2010-01-01 | JOURNAL OF ADOLESCENT HEALTH | - | 1.01 Articolo in rivista | - |
| 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 | - |
| Correlations of phenotype and genotype in relation to mor phologic remodelling of the aortic root in patients with Turner's syndrome | Prandstraller D; Mazzanti L; Giardini A; Lovato L; Tamburrino F; Scarano E; Cicognani A; Fattori ...R; Picchio FM | 2009-01-01 | CARDIOLOGY IN THE YOUNG | - | 1.01 Articolo in rivista | - |
| DEVELOPMENTAL SYNDROMES: GROWTH HORMONE DEFICIENCY AND TREATMENT. | Mazzanti, L; Tamburrino, F; Bergamaschi, R; Scarano, E; Montanari, F; Torella, M; Ballarini, E; C...icognani, A. | 2009-01-01 | - | Karger | 2.01 Capitolo / saggio in libro | - |
| Reproductive outcome in girls with congenital and acquired autoimmune thyroid pathology | Cassio, Alessandra; Bal, MILVA ORQUIDEA; S., Sansavini; E., Ballarini; F., Parata; Bettocchi, Ila...ria; Cicognani, Alessandro | 2009-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |