Výsledky vyhledávání - Marina Muzza
- Zobrazuji výsledky 1 - 7 z 7
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<i>DUOX2</i>/<i>DUOXA2</i> Mutations Frequently Cause Congenital Hypothyroidism that Evades Detection on Newborn Screening in the United Kingdom Autor Catherine Peters, Adeline K. Nicholas, Erik Schoenmakers, Greta Lyons, Shirley Langham, Eva Serra, Neil J. Sebire, Marina Muzza, Laura Fugazzola, Nadia Schoenmakers
Vydáno 2019Artigo -
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Radiofrequency ablation is an effective treatment for Bethesda III thyroid nodules without genetic alterations Autor Laura Fugazzola, Maurilio Deandrea, Stefano Borgato, Marco Dell’Acqua, Francesca Retta, Alberto Mormile, Chiara Carzaniga, Giacomo Gazzano, Gabriele Pogliaghi, Marina Muzza, Luca Persani
Vydáno 2024Artigo -
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The molecular and gene/miRNA expression profiles of radioiodine resistant papillary thyroid cancer Autor Carla Colombo, Emanuela Minna, Chiara Gargiuli, Marina Muzza, Matteo Dugo, Loris De Cecco, Gabriele Pogliaghi, Delfina Tosi, Gaetano Bulfamante, Angela Greco, Laura Fugazzola, Maria Grazia Borrello
Vydáno 2020Artigo -
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Modifications in the Papillary Thyroid Cancer Gene Profile Over the Last 15 Years Autor Cristina Romei, Laura Fugazzola, Efisio Puxeddu, Francesco Frasca, David Viola, Marina Muzza, Sonia Moretti, Maria Luisa Nicolosi, Carlotta Giani, Valentina Cirello, Nicola Avenia, Stefania Rossi, Paolo Vitti, Aldo Pinchera, Rossella Elisei
Vydáno 2012Artigo -
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The Clinical and Molecular Characterization of Patients With Dyshormonogenic Congenital Hypothyroidism Reveals Specific Diagnostic Clues for DUOX2 Defects Autor Marina Muzza, Sarah Rabbiosi, Maria Cristina Vigone, I. Zamproni, Valentina Cirello, Maria Antonia Maffini, Katia Maruca, Nadia Schoenmakers, Luciano Beccaria, Francesco Gallo, S.-M. Park, P. Beck‐Peccoz, Luca Persani, Giovanna Weber, Laura Fugazzola
Vydáno 2014Artigo
Vyhledávací nástroje:
Související témata
Internal medicine
Medicine
Thyroid
Biology
Thyroid cancer
Congenital hypothyroidism
Endocrinology
Gene
Genetics
Mutation
Oncology
Cancer
Cancer research
Missense mutation
Nonsense mutation
Papillary thyroid cancer
Pathology
Pediatrics
Thyroid nodules
Ablation
Astrobiology
Cohort
Compound heterozygosity
Exon
Follicular cell
Frameshift mutation
Gastroenterology
Incidence (geometry)
Liquid biopsy
Medullary cavity