Luca Persani

Table 1, Recorded cases of TSH-secreting adenomas of different type (updated end December 2012).

Paolo Beck-Peccoz, Luca Persani, Andrea Lania, 2015 .

GENETICS IN ENDOCRINOLOGY: Genetic diagnosis of endocrine diseases by NGS: novel scenarios and unpredictable results and risks.

Luca Persani, Tiziana de Filippis, Carla Colombo, 2018, European journal of endocrinology.

Functional Characterization of Wild-Type and a Mutated Form of SLC26A4 Identified in a Patient with Pendred Syndrome

Markus Ritter, Luca Persani, Johannes Fürst, 2006, Cellular Physiology and Biochemistry.

Fast Fluorometric Method for Measuring Pendrin (SLC26A4) Cl-/I- Transport Activity

Markus Ritter, Paolo Beck-Peccoz, Luca Persani, 2006, Cellular Physiology and Biochemistry.

Molecular and functional studies of 4 candidate loci in Pendred syndrome and nonsyndromic hearing loss

Paolo Beck-Peccoz, Luca Persani, P. Beck‐Peccoz, 2012, Molecular and Cellular Endocrinology.

Intracellular entrapment of wild-type TSH receptor by oligomerization with mutants linked to dominant TSH resistance.

Davide Calebiro, David Dunlap, Paolo Beck-Peccoz, 2005, Human molecular genetics.

An alternate translation initiation site circumvents an amino-terminal DAX1 nonsense mutation leading to a mild form of X-linked adrenal hypoplasia congenita.

John C Achermann, Paolo Beck-Peccoz, Luca Persani, 2003, The Journal of clinical endocrinology and metabolism.

Standardized Ultrasound Report for Thyroid Nodules: The Endocrinologist's Viewpoint

Luca Persani, M. Andrioli, L. Persani, 2013, European Thyroid Journal.

Interoceptive Axes Dissociation in Anorexia Nervosa: A Single Case Study With Follow Up Post-recovery Assessment

Giuseppe Riva, Silvia Serino, Luca Persani, 2019, Front. Psychol..