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Overview Leadership Blog JoVE Help Center

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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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M C Vigone

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Journal of Endocrinological Investigation|August 25, 2005

Congenital hypothyroidism with gland in situ: diagnostic re-evaluationG Weber, M C Vigone, A Passoni, et al.

American Journal of Medical Genetics|February 5, 1998

Comparison of clinical-radiological and molecular findings in hypochondroplasiaC Prinster, P Carrera, M Del Maschio, 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.

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Search research articles

Showing results (11-20 of 14) with videos related to

Sort By:

Pageof 2

You have reached the last page of results.This site can display upto 14 results.

Journal of Endocrinological Investigation|August 25, 2005

Congenital hypothyroidism with gland in situ: diagnostic re-evaluationG Weber, M C Vigone, A Passoni, et al.

American Journal of Medical Genetics|February 5, 1998

Comparison of clinical-radiological and molecular findings in hypochondroplasiaC Prinster, P Carrera, M Del Maschio, 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.

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