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Cancers|January 11, 2022
Retinal Glial Cells in Von Hippel-Lindau Disease: A Novel Approach in the Pathophysiology of Retinal HemangioblastomaElisabetta Pilotto, Giulia Midena, Tommaso Torresin, et al.
Thyroid : Official Journal of the American Thyroid Association|February 6, 2014
A novel mutation in the Albumin gene (R218S) causing familial dysalbuminemic hyperthyroxinemia in a family of Bangladeshi extractionSolomon Maximo Greenberg, Alfonso Massimiliano Ferrara, Everton S Nicholas, et al.
Plos One|August 12, 2022
Hyper-reflective retinal foci as possible in vivo imaging biomarker of microglia activation in von Hippel-Lindau diseaseElisabetta Pilotto, Tommaso Torresin, Maria Laura Bacelle, et al.
Endocrinology|May 23, 2013
Changes in thyroid status during perinatal development of MCT8-deficient male miceAlfonso Massimiliano Ferrara, Xiao-Hui Liao, Pilar Gil-Ibáñez, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|May 11, 2025
Euthyroid hyperthyroxinemia: relevance of albumin and transthyretin genetic variations in a single centre experienceIlaria Piva, Barollo Susi, Censi Simona, et al.
Thyroid : Official Journal of the American Thyroid Association|August 19, 2007
A new case of familial nonautoimmune hyperthyroidism caused by the M463V mutation in the TSH receptor with anticipation of the disease across generations: a possible role of iodine supplementationAlfonso Massimiliano Ferrara, Donatella Capalbo, Giuseppina Rossi, et al.
Thyroid : Official Journal of the American Thyroid Association|September 16, 2008
A novel NKX2.1 mutation in a family with hypothyroidism and benign hereditary choreaAlfonso Massimiliano Ferrara, Giuseppe De Michele, Elena Salvatore, et al.
International Journal of Molecular Sciences|March 10, 2022
Overexpression of miR-375 and L-type Amino Acid Transporter 1 in Pheochromocytoma and Their Molecular and Functional ImplicationsJacopo Manso, Loris Bertazza, Susi Barollo, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 2014
A novel mechanism of inherited TBG deficiency: mutation in a liver-specific enhancerAlfonso Massimiliano Ferrara, Theodora Pappa, Jiao Fu, et al.
Thyroid : Official Journal of the American Thyroid Association|February 6, 2013
Identification and functional characterization of a novel mutation in the NKX2-1 gene: comparison with the data in the literatureImmacolata Cristina Nettore, Paola Mirra, Alfonso Massimiliano Ferrara, et al.
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