Sfoglia per Autore
Peculiarities of Graves' disease in children and adolescents with Down's syndrome
2010-01-01 De Luca, Filippo; Corrias, Andrea; Salerno, Mariacarolina; Wasniewska, Malgorzata; Gastaldi, Roberto; Cassio, Alessandra; Mussa, Alessandro; Aversa, Tommaso; Radetti, Giorgio; Arrigo, Teresa
a microduplication of the centromeric domain of the 11p15.5 impirnted gene cluster is associated with loss of DNA methylation and familial BWS.
2010-01-01 Chiesa N; De Crescenzo N; Mussa A; Baldassarre G; Perone L; Carella M; Cirillo Silengo M; Riccio A; Ferrero GB
Frequency of Hashimoto's thyroiditis antecedents in the history of children and adolescents with Graves' disease
2010-01-01 Wasniewska, Malgorzata; Corrias, Andrea; Arrigo, Teresa; Lombardo, Fortunato; Salerno, Mariacarolina; Mussa, Alessandro; Vigone, Maria Cristina; De Luca, Filippo
Unresponsiveness to tetrahydrobiopterin of phenylalanine hydroxylase deficiency.
2010-01-01 Ponzone A; Porta F; Mussa A; Alluto A; Ferraris S; Spada M.
Graves' disease prevalence in a young population with Turner syndrome
2010-01-01 Wasniewska, M; Corrias, A; Messina, M F; Crisafulli, G; Salzano, G; Valenzise, M; Mussa, A; De Luca, F
Breastfeeding effects on newborn screening.
2010-01-01 Porta F; Mussa A; Ponzone A.
Bone quantitative ultrasound in congenital and acquired childhood multiple pituitary failure.
2010-01-01 Mussa A; Repici M; Fiore L; Tuli G; Porta F; Matarazzo P.
Diagnostic features of thyroid nodules in pediatrics
2010-01-01 Corrias, Andrea; Mussa, Alessandro; Baronio, Federico; Arrigo, Teresa; Salerno, Mariacarolina; Segni, Maria; Vigone, Maria Cristina; Gastaldi, Roberto; Zirilli, Giuseppa; Tuli, Gerdi; Beccaria, Luciano; Iughetti, Lorenzo; Einaudi, Silvia; Weber, Giovanna; De Luca, Filippo; Cassio, Alessandra
Fractures and skeletal complications should be the gold standard for validation of methods for bone appraisal in pediatrics
2010-01-01 Mussa A.; Bertorello N.; Porta F.; Galletto C.; Nicolosi M.G.; Manicone R.; Corrias A.; Fagioli F.
A heritable cause of cleft lip and palate-Van der Woude syndrome caused by a novel IRF6 mutation. Review of the literature and of the differential diagnosis.
2010-01-01 Ferrero GB; Baldassarre G; Panza E; Valenzise M; Pippucci T; Mussa A; Pepe E; Seri M; Silengo MC
The overlap between Sotos and Beckwith-Wiedemann syndromes
2010-01-01 Mussa A; Chiesa N; Porta F; Baldassarre G; Silengo MC; Ferrero GB.
Phalangeal quantitative ultrasound in 1,719 children and adolescents with bone disorders
2011-01-01 A. Mussa;F. Porta;G. Baldassarre;G. Tuli;F. Terlizzi;P. Matarazzo;S. Einaudi;R. Lala;A. Corrias
Determinants of thyrotropin rise in congenital hypothyroidism
2011-01-01 Alessandro Mussa;Francesco Porta; Giuseppina Baldassarre; Andrea Corrias
Levothyroxine treatment in pediatric benign thyroid nodules
2011-01-01 Corrias, Andrea; Mussa, Alessandro; Wasniewska, Malgorzata; Segni, Maria; Cassio, Alessandra; Salerno, Mariacarolina; Gastaldi, Roberto; Vigone, Maria Cristina; Bal, Milva; Matarazzo, Patrizia; Weber, Giovanna; De Luca, Filippo
Lysosomal enzyme activities in phenylketonuria.
2011-01-01 Porta F; Pagliardini S; Pagliardini V; Dotta A; Mussa A; Spada M.
Surgical enucleation of testicular leydigioma in a young child: case report and literature review
2011-01-01 Guanà, Riccardo; Mussa, Alessandro; Lala, Roberto; Tessaris, Daniele; Tessiatore, Patrizia Maiullari Erasmo; Canavese, Ferdinando
Phenotyping and treatment of phenylketonuria.
2011-01-01 Porta F; Mussa A; Garelli D; Spada M.
Prenatal features of Noonan syndrome: prevalence and prognostic value.
2011-01-01 Baldassarre G; Mussa A; Dotta A; Banaudi E; Forzano S; Marinosci A; Rossi C; Tartaglia M; Silengo M; Ferrero GB.
Neonatal hepatoblastoma in a newborn with severe phenotype of Beckwith-Wiedemann syndrome.
2011-01-01 Mussa A; Ferrero GB; Ceoloni B; Basso E; Chiesa N; De Crescenzo A; Pepe E; Silengo M; de Sanctis L.
Tetrahydrobiopterin and phenylketonuria.
2011-01-01 Porta F; Spada M; Garelli D; Mussa A; Ponzone A.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Peculiarities of Graves' disease in children and adolescents with Down's syndrome | 2010 | De Luca, Filippo; Corrias, Andrea; Salerno, Mariacarolina; Wasniewska, Malgorzata; Gastaldi, Roberto; Cassio, Alessandra; Mussa, Alessandro; Aversa, Tommaso; Radetti, Giorgio; Arrigo, Teresa | |
| a microduplication of the centromeric domain of the 11p15.5 impirnted gene cluster is associated with loss of DNA methylation and familial BWS. | 2010 | Chiesa N; De Crescenzo N; Mussa A; Baldassarre G; Perone L; Carella M; Cirillo Silengo M; Riccio A; Ferrero GB | |
| Frequency of Hashimoto's thyroiditis antecedents in the history of children and adolescents with Graves' disease | 2010 | Wasniewska, Malgorzata; Corrias, Andrea; Arrigo, Teresa; Lombardo, Fortunato; Salerno, Mariacarolina; Mussa, Alessandro; Vigone, Maria Cristina; De Luca, Filippo | |
| Unresponsiveness to tetrahydrobiopterin of phenylalanine hydroxylase deficiency. | 2010 | Ponzone A; Porta F; Mussa A; Alluto A; Ferraris S; Spada M. | |
| Graves' disease prevalence in a young population with Turner syndrome | 2010 | Wasniewska, M; Corrias, A; Messina, M F; Crisafulli, G; Salzano, G; Valenzise, M; Mussa, A; De Luca, F | |
| Breastfeeding effects on newborn screening. | 2010 | Porta F; Mussa A; Ponzone A. | |
| Bone quantitative ultrasound in congenital and acquired childhood multiple pituitary failure. | 2010 | Mussa A; Repici M; Fiore L; Tuli G; Porta F; Matarazzo P. | |
| Diagnostic features of thyroid nodules in pediatrics | 2010 | Corrias, Andrea; Mussa, Alessandro; Baronio, Federico; Arrigo, Teresa; Salerno, Mariacarolina; Segni, Maria; Vigone, Maria Cristina; Gastaldi, Roberto; Zirilli, Giuseppa; Tuli, Gerdi; Beccaria, Luciano; Iughetti, Lorenzo; Einaudi, Silvia; Weber, Giovanna; De Luca, Filippo; Cassio, Alessandra | |
| Fractures and skeletal complications should be the gold standard for validation of methods for bone appraisal in pediatrics | 2010 | Mussa A.; Bertorello N.; Porta F.; Galletto C.; Nicolosi M.G.; Manicone R.; Corrias A.; Fagioli F. | |
| A heritable cause of cleft lip and palate-Van der Woude syndrome caused by a novel IRF6 mutation. Review of the literature and of the differential diagnosis. | 2010 | Ferrero GB; Baldassarre G; Panza E; Valenzise M; Pippucci T; Mussa A; Pepe E; Seri M; Silengo MC | |
| The overlap between Sotos and Beckwith-Wiedemann syndromes | 2010 | Mussa A; Chiesa N; Porta F; Baldassarre G; Silengo MC; Ferrero GB. | |
| Phalangeal quantitative ultrasound in 1,719 children and adolescents with bone disorders | 2011 | A. Mussa;F. Porta;G. Baldassarre;G. Tuli;F. Terlizzi;P. Matarazzo;S. Einaudi;R. Lala;A. Corrias | |
| Determinants of thyrotropin rise in congenital hypothyroidism | 2011 | Alessandro Mussa;Francesco Porta; Giuseppina Baldassarre; Andrea Corrias | |
| Levothyroxine treatment in pediatric benign thyroid nodules | 2011 | Corrias, Andrea; Mussa, Alessandro; Wasniewska, Malgorzata; Segni, Maria; Cassio, Alessandra; Salerno, Mariacarolina; Gastaldi, Roberto; Vigone, Maria Cristina; Bal, Milva; Matarazzo, Patrizia; Weber, Giovanna; De Luca, Filippo | |
| Lysosomal enzyme activities in phenylketonuria. | 2011 | Porta F; Pagliardini S; Pagliardini V; Dotta A; Mussa A; Spada M. | |
| Surgical enucleation of testicular leydigioma in a young child: case report and literature review | 2011 | Guanà, Riccardo; Mussa, Alessandro; Lala, Roberto; Tessaris, Daniele; Tessiatore, Patrizia Maiullari Erasmo; Canavese, Ferdinando | |
| Phenotyping and treatment of phenylketonuria. | 2011 | Porta F; Mussa A; Garelli D; Spada M. | |
| Prenatal features of Noonan syndrome: prevalence and prognostic value. | 2011 | Baldassarre G; Mussa A; Dotta A; Banaudi E; Forzano S; Marinosci A; Rossi C; Tartaglia M; Silengo M; Ferrero GB. | |
| Neonatal hepatoblastoma in a newborn with severe phenotype of Beckwith-Wiedemann syndrome. | 2011 | Mussa A; Ferrero GB; Ceoloni B; Basso E; Chiesa N; De Crescenzo A; Pepe E; Silengo M; de Sanctis L. | |
| Tetrahydrobiopterin and phenylketonuria. | 2011 | Porta F; Spada M; Garelli D; Mussa A; Ponzone A. |
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