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Vera Stoppioni

Research Profile

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Newborn Infant

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Alessandra Cassio; G Cesaretti; Carlo Corbetta; R Gastaldi; E Medda; F Mosca; A Olivieri; E Pasquini; M C Salerno; Vera Stoppioni; M Tonacchera; G Weber; I Antonozzi; Francesca Calaciura; U Caruso
The Italian screening program for primary congenital hypothyroidism: actions to improve screening, diagnosis, follow-up, and surveillance.
Marco B L Rocchi; Davide Sisti; Maria Cristina Albertini; Giulia Burroni; Vera Stoppioni; Renzo Ciatti; Massimo Burroni
Geographical epidemiology of neonatal transitory hypothyroidism. Trend evidence in central Italian region.
Monica Dentice; Viviana Cordeddu; Annamaria Rosica; Alfonso Massimiliano Ferrara; Libero Santarpia; Domenico Salvatore; Luca Chiovato; Anna Perri; Lidia Moschini; Cristina Fazzini; Antonella Olivieri; Pietro Costa; Vera Stoppioni; Mariangiola Baserga; Mario De Felice; Mariella Sorcini; Gianfranco Fenzi; Roberto Di Lauro; Marco Tartaglia; Paolo Emidio Macchia
Missense mutation in the transcription factor NKX2-5: a novel molecular event in the pathogenesis of thyroid dysgenesis.

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All Publications

2013: Alessandra Cassio; G Cesaretti; Carlo Corbetta; R Gastaldi; E Medda; F Mosca; A Olivieri; E Pasquini; M C Salerno; Vera Stoppioni; M Tonacchera; G Weber; I Antonozzi; Francesca Calaciura; U Caruso
The Italian screening program for primary congenital hypothyroidism: actions to improve screening, diagnosis, follow-up, and surveillance.
Journal of endocrinological investigation 2013;36(3):195-203.
2008: Marco B L Rocchi; Davide Sisti; Maria Cristina Albertini; Giulia Burroni; Vera Stoppioni; Renzo Ciatti; Massimo Burroni
Geographical epidemiology of neonatal transitory hypothyroidism. Trend evidence in central Italian region.
Journal of pediatric endocrinology & metabolism : JPEM 2008;21(4):377-80.
2006: Monica Dentice; Viviana Cordeddu; Annamaria Rosica; Alfonso Massimiliano Ferrara; Libero Santarpia; Domenico Salvatore; Luca Chiovato; Anna Perri; Lidia Moschini; Cristina Fazzini; Antonella Olivieri; Pietro Costa; Vera Stoppioni; Mariangiola Baserga; Mario De Felice; Mariella Sorcini; Gianfranco Fenzi; Roberto Di Lauro; Marco Tartaglia; Paolo Emidio Macchia
Missense mutation in the transcription factor NKX2-5: a novel molecular event in the pathogenesis of thyroid dysgenesis.
The Journal of clinical endocrinology and metabolism 2006;91(4):1428-33.
2005: Emanuela Medda; Antonella Olivieri; Maria Antonietta Stazi; Michele E Grandolfo; Cristina Fazzini; Mariangiola Baserga; Massimo Burroni; Emanuele Cacciari; Francesca Calaciura; Alessandra Cassio; Luca Chiovato; Pietro Costa; Daniela Leonardi; Maria Martucci; Lidia Moschini; Severo Pagliardini; Giuseppe Parlato; Alberto Pignero; Aldo Pinchera; Danielle Sala; Lidia Sava; Vera Stoppioni; Francesco Tancredi; Fabiola Valentini; Riccardo Vigneri; Mariella Sorcini
Risk factors for congenital hypothyroidism: results of a population case-control study (1997-2003).
European journal of endocrinology / European Federation of Endocrine Societies 2005;153(6):765-73.
2003: Malgorzata Wasniewska; Filippo De Luca; Alessandra Cassio; Nicola Oggiaro; Paola Gianino; Maurizio Delvecchio; Rosalba Aiazzi; Vera Stoppioni; Fortunato Lombardo; Maria Francesca Messina; Mariella Valenzise; Teresa Arrigo
In congenital hypothyroidism bone maturation at birth may be a predictive factor of psychomotor development during the first Year of life irrespective of other variables related to treatment.
European journal of endocrinology / European Federation of Endocrine Societies 2003;149(1):1-6.