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M Muzza

Showing results (1-10 of 4) with videos related to

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Journal of Endocrinological Investigation|December 20, 2019
Molecular markers for the classification of cytologically indeterminate thyroid nodulesM Muzza, C Colombo, G Pogliaghi, et al.
Annales D'Endocrinologie|April 23, 2011
DUOXS defects: Genotype-phenotype correlationsL Fugazzola, M Muzza, G Weber, et al.
Journal of Endocrinological Investigation|September 7, 2022
Stochastic epigenetic mutations as possible explanation for phenotypical discordance among twins with congenital hypothyroidismD Gentilini, M Muzza, T de Filippis, et al.
The Journal of Clinical Endocrinology and Metabolism|January 16, 2014
The clinical and molecular characterization of patients with dyshormonogenic congenital hypothyroidism reveals specific diagnostic clues for DUOX2 defectsM Muzza, S Rabbiosi, M C Vigone, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Journal of Endocrinological Investigation|December 20, 2019
Molecular markers for the classification of cytologically indeterminate thyroid nodulesM Muzza, C Colombo, G Pogliaghi, et al.
Annales D'Endocrinologie|April 23, 2011
DUOXS defects: Genotype-phenotype correlationsL Fugazzola, M Muzza, G Weber, et al.
Journal of Endocrinological Investigation|September 7, 2022
Stochastic epigenetic mutations as possible explanation for phenotypical discordance among twins with congenital hypothyroidismD Gentilini, M Muzza, T de Filippis, et al.
The Journal of Clinical Endocrinology and Metabolism|January 16, 2014
The clinical and molecular characterization of patients with dyshormonogenic congenital hypothyroidism reveals specific diagnostic clues for DUOX2 defectsM Muzza, S Rabbiosi, M C Vigone, et al.
Pageof 1