A. Panarotto

发表

A novel menin gene deletional mutation in a little series of Italian patients affected by apparently sporadic multiple endocrine neoplasia type 1 syndrome

M. Castellano, E. Agabiti Rosei, I. Pirola, 2012, Journal of Endocrinological Investigation.

Genetic Mutation Screening in an Italian Cohort of Nonsyndromic Pheochromocytoma/Paraganglioma Patients

M. Castellano, C. Cappelli, F. Veglio, 2006, Annals of the New York Academy of Sciences.

p.Ser891Ala RET gene mutations in medullary thyroid cancer: Phenotypical and genealogical characterization of 28 apparently unrelated kindreds and founder effect uncovering in Northern Italy

M. Castellano, C. Cappelli, I. Pirola, 2019, Human mutation.

New pathogenic variants in ARMC5 gene in a series of Italian patients affected by primary bilateral macronodular adrenocortical hyperplasia (PBMAH)

P. L. Poliani, L. Mori, M. Giacché, 2023, Molecular genetics & genomic medicine.