La resistenza e le altre sindromi da ridotta sensibilità agli ormoni tiroidei von Di Cosmo, Caterina

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Distinct Roles of Deiodinases on the Phenotype of Mct8 Defect: A Comparison of Eight Different Mouse Genotypes von Liao, Xiao-Hui, Di Cosmo, Caterina, Dumitrescu, Alexandra M, Hernandez, Arturo, Van Sande, Jacqueline, St. Germain, Donald L, Weiss, Roy E, Galton, Valerie Anne, Refetoff, Samuel

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The syndrome of inherited partial SBP2 deficiency in humans von Dumitrescu, Alexandra M, Di Cosmo, Caterina, Liao, Xiao-Hui, Weiss, Roy E, Refetoff, Samuel

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A Combined Therapy with Myo-Inositol and D-Chiro-Inositol Improves Endocrine Parameters and Insulin Resistance in PCOS Young Overweight Women von Tonacchera, Massimo, Di Cosmo, Caterina, Del Ghianda, Scilla, Benelli, Elena

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Clinical features, risk of mass enlargement, and development of endocrine hyperfunction in patients with adrenal incidentalomas: a long-term follow-up study von Falcetta, Pierpaolo, Orsolini, Francesca, Benelli, Elena, Agretti, Patrizia, Vitti, Paolo, Di Cosmo, Caterina, Tonacchera, Massimo

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Mice deficient in MCT8 reveal a mechanism regulating thyroid hormone secretion von Di Cosmo, Caterina, Liao, Xiao-Hui, Dumitrescu, Alexandra M, Philp, Nancy J, Weiss, Roy E, Refetoff, Samuel

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Diiodothyropropionic Acid (DITPA) in the Treatment of MCT8 Deficiency von Verge, Charles F, Konrad, Daniel, Cohen, Michal, Di Cosmo, Caterina, Dumitrescu, Alexandra M, Marcinkowski, Teresa, Hameed, Shihab, Hamilton, Jill, Weiss, Roy E, Refetoff, Samuel

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Thyroid Hormone-Regulated Mouse Cerebral Cortex Genes Are Differentially Dependent on the Source of the Hormone: A Study in Monocarboxylate Transporter-8- and Deiodinase-2-Deficien... von Morte, Beatriz, Ceballos, Ainhoa, Diez, Diego, Grijota-Martínez, Carmen, Dumitrescu, Alexandra M, Di Cosmo, Caterina, Galton, Valerie Anne, Refetoff, Samuel, Bernal, Juan

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Mct8-Deficient Mice Have Increased Energy Expenditure and Reduced Fat Mass That Is Abrogated by Normalization of Serum T3 Levels von Di Cosmo, Caterina, Liao, Xiao-Hui, Ye, Honggang, Ferrara, Alfonso Massimiliano, Weiss, Roy E, Refetoff, Samuel, Dumitrescu, Alexandra M

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Late-onset dyshormonogenic goitrous hypothyroidism due to a homozygous mutation of the SLC26A7 gene: a case report von Sciarroni, Elisabetta, Montanelli, Lucia, Di Cosmo, Caterina, Bagattini, Brunella, Comi, Simone, Pignata, Luisa, Brancatella, Alessandro, De Marco, Giuseppina, Ferrarini, Eleonora, Nencetti, Chiara, Sessa, Maria Rita, Latrofa, Francesco, Santini, Ferruccio, Tonacchera, Massimo, Agretti, Patrizia

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A Thyroid Hormone Analog with Reduced Dependence on the Monocarboxylate Transporter 8 for Tissue Transport von Di Cosmo, Caterina, Liao, Xiao-Hui, Dumitrescu, Alexandra M, Weiss, Roy E, Refetoff, Samuel

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Clinical and Molecular Characterization of a Novel Selenocysteine Insertion Sequence-Binding Protein 2 (SBP2) Gene Mutation (R128X) von Di Cosmo, Caterina, McLellan, Neil, Liao, Xiao-Hui, Khanna, Kum Kum, Weiss, Roy E., Papp, Laura, Refetoff, Samuel

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An Essential Physiological Role for MCT8 in Bone in Male Mice von Leitch, Victoria D, Di Cosmo, Caterina, Liao, Xiao-Hui, O’Boy, Sam, Galliford, Thomas M, Evans, Holly, Croucher, Peter I, Boyde, Alan, Dumitrescu, Alexandra, Weiss, Roy E, Refetoff, Samuel, Williams, Graham R, Bassett, J H Duncan

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Papillary thyroid cancer in a patient with congenital goitrous hypothyroidism due to a novel deletion in NIS gene von Agretti, Patrizia, Bagattini, Brunella, De Marco, Giuseppina, Di Cosmo, Caterina, Dionigi, Gianlorenzo, Vitti, Paolo, Tonacchera, Massimo

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Identification and Functional Analysis of Novel Dual Oxidase 2 (DUOX2) Mutations in Children with Congenital or Subclinical Hypothyroidism von De Marco, Giuseppina, Agretti, Patrizia, Montanelli, Lucia, Di Cosmo, Caterina, Bagattini, Brunella, De Servi, Melissa, Ferrarini, Eleonora, Dimida, Antonio, Freitas Ferreira, Andrea Claudia, Molinaro, Angelo, Ceccarelli, Claudia, Brozzi, Federica, Pinchera, Aldo, Vitti, Paolo, Tonacchera, Massimo

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Disruption of the Melanin-Concentrating Hormone Receptor 1 (MCH1R) Affects Thyroid Function von Chung, Shinjae, Liao, Xiao-Hui, Di Cosmo, Caterina, Van Sande, Jacqueline, Wang, Zhiwei, Refetoff, Samuel, Civelli, Olivier

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A Not So Benign Family Pedigree With Hereditary Chorea: A Broader Phenotypic Expression or Additional Picture? von Milone, Roberta, Masson, Riccardo, Di Cosmo, Caterina, Tonacchera, Massimo, Bertini, Veronica, Guzzetta, Andrea, Battini, Roberta

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Clinical course of congenital hypothyroidism with gland in situ and necessity of L-thyroxine therapy after re-evaluation von Pignata, Luisa, Bagattini, Brunella, Di Cosmo, Caterina, Agretti, Patrizia, De Marco, Giuseppina, Ferrarini, Eleonora, Montanelli, Lucia, Tonacchera, Massimo

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Manifestazioni cliniche delle mutazioni del trasportatore degli ormoni tiroidei MCT8: Proposto da Aldo Pinchera von Di Cosmo, Caterina

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The different requirement of l-T4 therapy in congenital athyreosis compared with adult-acquired hypothyroidism suggests a persisting thyroid hormone resistance at the hypothalamic–... von Bagattini, Brunella, Cosmo, Caterina Di, Montanelli, Lucia, Piaggi, Paolo, Ciampi, Mariella, Agretti, Patrizia, Marco, Giuseppina De, Vitti, Paolo, Tonacchera, Massimo

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