BERGAMASCHI, ROSALBA
BERGAMASCHI, ROSALBA
DIPARTIMENTO DI SCIENZE MEDICHE E CHIRURGICHE
BERGAMASCHI R; BERGAMASCHI ROSALBA; R.BERGAMASCHI; ROSALBA BERGAMASCHI
A mutation in PAK3 with a dual molecular effect deregulates the RAS/MAPK pathway and drives an X-linked syndromic phenotype.
2014 Magini P;Pippucci T;Tsai IC;Coppola S;Stellacci E;Bartoletti-Stella A;Turchetti D;Graziano C;Cenacchi G;Neri I;Cordelli DM;Marchiani V;Bergamaschi R;Gasparre G;Neri G;Mazzanti L;Patrizi A;Franzoni E;Romeo G;Bordo D;Tartaglia M;Katsanis N;Seri M
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
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
Acute Hemiplegia and Facial Palsy 4-Months after Acute Kawasaki Disease in a 31-Month Old Girl
2014 Davide Tassinari; Michela Maretti; Claudia Balsamo; Rosalba Bergamaschi; Filomena Carfagnini; Marianna Fabi; Filippo Bernardi
Acute mastoiditis in an Italian pediatric tertiary medical center: A 15 - Year retrospective study
2018 Balsamo, Claudia*; Biagi, Carlotta; Mancini, Margherita; Corsini, Ilaria; Bergamaschi, Rosalba; Lanari, Marcello
Carbonic anhydrase II deficiency: A rare case of severe obstructive sleep apnea
2018 di Palmo, Emanuela; Gallucci, Marcella; Tronconi, Elena; Bergamaschi, Rosalba; Cazzato, Salvatore; La Scola, Claudio; Ricci, Giampaolo*; Pession, Andrea
DEVELOPMENTAL SYNDROMES: GROWTH HORMONE DEFICIENCY AND TREATMENT.
2009 Mazzanti, L; Tamburrino, F; Bergamaschi, R; Scarano, E; Montanari, F; Torella, M; Ballarini, E; Cicognani, A.
EARLY TREATMENT WITH GH ALONE IN TURNER SYNDROME: PREPUBERTAL CATCH-UP GROWTH AND WANING EFFECT.
2004 Wasniewska M.; De Luca F.; Bergamaschi R.; Guarneri MP.; Mazzanti L.; Matarazzo P.; Petri A.; Crisafulli G.; Salzano G.; Lombardo F.
Glucose tolerance and insulin sensitivity in Turner patients treated with GH: Follow-up until the young adult age
2005 L. Mazzanti;R. Bergamaschi;E. Scarano;M. Bal;L. Castiglioni;C. Matteucci;F.Tamburrino;F. Zappulla ; A. Cicognani
Gonadoblastoma in Turner syndrome and Y-chromosome-derived material.
2005 Mazzanti L; Cicognani A; Baldazzi L; Bergamaschi R; Scarano E; Strocchi S; Nicoletti A; Mencarelli F; Pittalis M; Forabosco A; Cacciari E.
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
Hearing loss in Turner syndrome: results of a multicentric study.
2008 Bergamaschi R; Bergonzoni C; Mazzanti L; Scarano E; Mencarelli F; Messina F;Rosano M; Iughetti L; Cicognani A.
Increased liver enzymes and hormonal therapies in girls and adolescents with Turner syndrome.
2005 Wasniewska M; Bergamaschi R; Matarazzo P; Predieri B; Bertelloni S; Petri A;Sposito M; Messina MF; De Luca F
Interstitial 6q deletion: a new patient with empty sella and GH deficiency
2007 Emanuela Scarano; Laura Mazzanti; Marco Seri; Rosalba Bergamaschi; Chiara Matteucci; Pamela Magini; Manuela de Gregori; Roberto Ciccone; Orsetta Zuffardi; Alessandro Cicognani
Juvenile dermatomyositis: A report of three cases
2016 Papa, V; Romanin, B; Bergamaschi, R; Cordelli, Dm; Costa, R; De Giorgi, Lb; Cenacchi, G
Lymphocyte TRPV 1-4 gene expression and MIF blood levels in a young girl clinically diagnosed with HSAN IV.
2011 Bachiocco V; Bergamaschi R; Spinsanti G; Lima M; Romagnoli R; Sorda G; Aloisi AM
Mowat-Wilson syndrome: Facial phenotype changing with age: Study of 19 Italian patients and review of the literature
2009 Garavelli L.; Zollino M.; Cerruti Mainardi P.; Gurrieri F.; Rivieri F.; Soli F.; Verri R.; Albertini E.; Favaron E.; Zignani M.; Orteschi D.; Bianchi P.; Faravelli F.; Forzano F.; Seri M.; Wischmeijer A.; Turchetti D.; Pompilii E.; Gnoli M.; Cocchi G.; Mazzanti L.; Bergamaschi R.; De Brasi D.; Sperandeo M.P.; Mari F.; Uliana V.; Mostardini R.; Cecconi M.; Grasso M.; Sassi S.; Sebastio G.; Renieri A.; Silengo M.; Bernasconi S.; Wakamatsu N.; Neri G.
Noonan syndrome and PTPN11 mutations: clinical findings and growth follow-up with long-term GH therapy
2007 Laura Mazzanti; Emanuela Scarano; Rosalba Bergamaschi; Cesare Rossi; Chiara Matteucci; Federica Tamburrino; Piero Pirazzoli; Francesca Mencarelli; Alessandro Cicognani
Posterior Reversible Encephalopathy Syndrome Associated With Licorice Consumption: A Case Report in a 10-Year-Old Boy
2015 Davide Tassinari;Rosalba Bergamaschi;Ilaria Corsini;Susanna Landini;Benedetta Romanin;Elisa Ballarini;Fabrizio De Ponti;Filomena Carfagnini;Francesco Toni;Filippo Bernardi
Prevalence of Aortic Dilation in Turner Patients without Congenital Heart Disease (CHD) Studied at Echocardiography and Transthoracic MRI
2004 L. Mazzanti; D. Prandstraller; R. Bergamaschi; R. Fattori; E. Scarano; F. Mencarelli; S. Strocchi; V. Rosetti; D. Tassinari; A. Cicognani; E. Cacciari
Titolo | Autore(i) | Anno | Periodico | Editore | Tipo | File |
---|---|---|---|---|---|---|
A mutation in PAK3 with a dual molecular effect deregulates the RAS/MAPK pathway and drives an X-linked syndromic phenotype. | Magini P;Pippucci T;Tsai IC;Coppola S;Stellacci E;Bartoletti-Stella A;Turchetti D;Graziano C;Cena...cchi G;Neri I;Cordelli DM;Marchiani V;Bergamaschi R;Gasparre G;Neri G;Mazzanti L;Patrizi A;Franzoni E;Romeo G;Bordo D;Tartaglia M;Katsanis N;Seri M | 2014-01-01 | HUMAN MOLECULAR GENETICS | - | 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 | - |
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) | - |
Acute Hemiplegia and Facial Palsy 4-Months after Acute Kawasaki Disease in a 31-Month Old Girl | Davide Tassinari; Michela Maretti; Claudia Balsamo; Rosalba Bergamaschi; Filomena Carfagnini; Mar...ianna Fabi; Filippo Bernardi | 2014-01-01 | JSM CLINICAL CASE REPORTS | - | 1.01 Articolo in rivista | - |
Acute mastoiditis in an Italian pediatric tertiary medical center: A 15 - Year retrospective study | Balsamo, Claudia*; Biagi, Carlotta; Mancini, Margherita; Corsini, Ilaria; Bergamaschi, Rosalba; L...anari, Marcello | 2018-01-01 | THE ITALIAN JOURNAL OF PEDIATRICS | - | 1.01 Articolo in rivista | - |
Carbonic anhydrase II deficiency: A rare case of severe obstructive sleep apnea | di Palmo, Emanuela; Gallucci, Marcella; Tronconi, Elena; Bergamaschi, Rosalba; Cazzato, Salvatore...; La Scola, Claudio; Ricci, Giampaolo*; Pession, Andrea | 2018-01-01 | FRONTIERS IN PEDIATRICS | - | 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 | - |
EARLY TREATMENT WITH GH ALONE IN TURNER SYNDROME: PREPUBERTAL CATCH-UP GROWTH AND WANING EFFECT. | Wasniewska M.; De Luca F.; Bergamaschi R.; Guarneri MP.; Mazzanti L.; Matarazzo P.; Petri A.; Cri...safulli G.; Salzano G.; Lombardo F. | 2004-01-01 | EUROPEAN JOURNAL OF ENDOCRINOLOGY | - | 1.01 Articolo in rivista | - |
Glucose tolerance and insulin sensitivity in Turner patients treated with GH: Follow-up until the young adult age |
L. Mazzanti;R. Bergamaschi;E. Scarano;M. Bal;L. Castiglioni;C. Matteucci;F.Tamburrino;F. Zappulla... ; A. Cicognani |
2005-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
Gonadoblastoma in Turner syndrome and Y-chromosome-derived material. | Mazzanti L; Cicognani A; Baldazzi L; Bergamaschi R; Scarano E; Strocchi S; Nicoletti A; Mencarell...i F; Pittalis M; Forabosco A; Cacciari E. | 2005-01-01 | AMERICAN JOURNAL OF MEDICAL GENETICS. PART A | - | 1.01 Articolo in rivista | - |
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 | - |
Hearing loss in Turner syndrome: results of a multicentric study. | Bergamaschi R; Bergonzoni C; Mazzanti L; Scarano E; Mencarelli F; Messina F;Rosano M; Iughetti L;... Cicognani A. | 2008-01-01 | JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION | - | 1.01 Articolo in rivista | - |
Increased liver enzymes and hormonal therapies in girls and adolescents with Turner syndrome. | Wasniewska M; Bergamaschi R; Matarazzo P; Predieri B; Bertelloni S; Petri A;Sposito M; Messina MF...; De Luca F | 2005-01-01 | JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION | - | 1.01 Articolo in rivista | - |
Interstitial 6q deletion: a new patient with empty sella and GH deficiency |
Emanuela Scarano; Laura Mazzanti; Marco Seri; Rosalba Bergamaschi; Chiara Matteucci; Pamela Magi...ni; Manuela de Gregori; Roberto Ciccone; Orsetta Zuffardi; Alessandro Cicognani |
2007-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
Juvenile dermatomyositis: A report of three cases | Papa, V; Romanin, B; Bergamaschi, R; Cordelli, Dm; Costa, R; De Giorgi, Lb; Cenacchi, G | 2016-01-01 | ULTRASTRUCTURAL PATHOLOGY | - | 1.01 Articolo in rivista | - |
Lymphocyte TRPV 1-4 gene expression and MIF blood levels in a young girl clinically diagnosed with HSAN IV. | Bachiocco V; Bergamaschi R; Spinsanti G; Lima M; Romagnoli R; Sorda G; Aloisi AM | 2011-01-01 | THE CLINICAL JOURNAL OF PAIN | - | 1.01 Articolo in rivista | - |
Mowat-Wilson syndrome: Facial phenotype changing with age: Study of 19 Italian patients and review of the literature | Garavelli L.; Zollino M.; Cerruti Mainardi P.; Gurrieri F.; Rivieri F.; Soli F.; Verri R.; Albert...ini E.; Favaron E.; Zignani M.; Orteschi D.; Bianchi P.; Faravelli F.; Forzano F.; Seri M.; Wischmeijer A.; Turchetti D.; Pompilii E.; Gnoli M.; Cocchi G.; Mazzanti L.; Bergamaschi R.; De Brasi D.; Sperandeo M.P.; Mari F.; Uliana V.; Mostardini R.; Cecconi M.; Grasso M.; Sassi S.; Sebastio G.; Renieri A.; Silengo M.; Bernasconi S.; Wakamatsu N.; Neri G. | 2009-01-01 | AMERICAN JOURNAL OF MEDICAL GENETICS. PART A | - | 1.01 Articolo in rivista | - |
Noonan syndrome and PTPN11 mutations: clinical findings and growth follow-up with long-term GH therapy |
Laura Mazzanti; Emanuela Scarano; Rosalba Bergamaschi; Cesare Rossi; Chiara Matteucci; Federica ...Tamburrino; Piero Pirazzoli; Francesca Mencarelli; Alessandro Cicognani |
2007-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |
Posterior Reversible Encephalopathy Syndrome Associated With Licorice Consumption: A Case Report in a 10-Year-Old Boy | Davide Tassinari;Rosalba Bergamaschi;Ilaria Corsini;Susanna Landini;Benedetta Romanin;Elisa Balla...rini;Fabrizio De Ponti;Filomena Carfagnini;Francesco Toni;Filippo Bernardi | 2015-01-01 | PEDIATRIC NEUROLOGY | - | 1.01 Articolo in rivista | - |
Prevalence of Aortic Dilation in Turner Patients without Congenital Heart Disease (CHD) Studied at Echocardiography and Transthoracic MRI |
L. Mazzanti; D. Prandstraller; R. Bergamaschi; R. Fattori; E. Scarano; F. Mencarelli; S. Strocch...i; V. Rosetti; D. Tassinari; A. Cicognani; E. Cacciari |
2004-01-01 | HORMONE RESEARCH | - | 4.02 Riassunto (Abstract) | - |