A. Ferrara

发表

Pheochromocytomas in Complex Genetic Disorders

G. Opocher, F. Schiavi, G. Barbon, 2021, Endocrinology.

Pheochromocytomas in Complex Genetic Disorders

G. Opocher, F. Schiavi, G. Barbon, 2019, Endocrinology.

Missense mutation in the transcription factor NKX2-5: a novel molecular event in the pathogenesis of thyroid dysgenesis.

V. Stoppioni, P. Macchia, L. Chiovato, 2006, The Journal of clinical endocrinology and metabolism.

Mct8-deficient mice have increased energy expenditure and reduced fat mass that is abrogated by normalization of serum T3 levels.

R. Weiss, S. Refetoff, X. Liao, 2013, Endocrinology.

Mutations in TAZ/WWTR1, a co-activator of NKX2.1 and PAX8 are not a frequent cause of thyroid dysgenesis

P. Macchia, M. Zannini, G. Fenzi, 2009, Journal of endocrinological investigation.

Benign hereditary chorea: Clinical and neuroimaging features in an Italian family

S. Pappatà, P. Macchia, G. De Michele, 2010, Movement disorders : official journal of the Movement Disorder Society.

A novel NKX2.1 mutation in a family with hypothyroidism and benign hereditary chorea.

P. Macchia, G. De Michele, A. Filla, 2008, Thyroid : official journal of the American Thyroid Association.

Medication-related osteonecrosis of the jaw in patients with bone metastases from solid tumors: analysis of the Istituto Oncologico Veneto case series

V. Zagonel, A. Brunello, V. Guarneri, 2021 .

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 supplementation.

P. Macchia, G. Fenzi, M. Salerno, 2007, Thyroid : official journal of the American Thyroid Association.

Screening for mutations in the ISL1 gene in patients with thyroid dysgenesis

P. Macchia, I. C. Nettore, G. Fenzi, 2011, Journal of endocrinological investigation.

Inherited defects of thyroxine-binding proteins.

S. Refetoff, T. Pappa, A. Ferrara, 2015, Best practice & research. Clinical endocrinology & metabolism.

Retinal Glial Cells in Von Hippel–Lindau Disease: A Novel Approach in the Pathophysiology of Retinal Hemangioblastoma

E. Pilotto, E. Midena, S. zovato, 2021, Cancers.

The DREAM protein is associated with thyroid enlargement and nodular development.

M. Zannini, Begoña Torres, B. Mellström, 2009, Molecular endocrinology.

Development The DREAM Protein Is Associated with Thyroid Enlargement and Nodular

Begoña Torres, J. Naranjo, D. Terracciano, 2009 .

A somatic gain-of-function mutation in the thyrotropin receptor gene producing a toxic adenoma in an infant.

B. Kohn, S. Refetoff, H. Grasberger, 2009, Thyroid : official journal of the American Thyroid Association.

Hyper-reflective retinal foci as possible in vivo imaging biomarker of microglia activation in von Hippel-Lindau disease

E. Pilotto, E. Midena, S. zovato, 2022, PloS one.

Comparison of Pheochromocytoma-Specific Morbidity and Mortality Among Adults With Bilateral Pheochromocytomas Undergoing Total Adrenalectomy vs Cortical-Sparing Adrenalectomy

W. Young, C. Eng, T. Krauss, 2019, JAMA network open.

Overexpression of miR-375 and L-type Amino Acid Transporter 1 in Pheochromocytoma and Their Molecular and Functional Implications

S. Barollo, L. Bertazza, G. Pennelli, 2022, International journal of molecular sciences.

A novel mutation in the Albumin gene (R218S) causing familial dysalbuminemic hyperthyroxinemia in a family of Bangladeshi extraction.

V. Cody, R. Weiss, S. Refetoff, 2014, Thyroid : official journal of the American Thyroid Association.

A novel mechanism of inherited TBG deficiency: mutation in a liver-specific enhancer.

Christopher D. Brown, K. White, M. Nóbrega, 2015, The Journal of clinical endocrinology and metabolism.