M. Baserga

发表

Cross-sectional reference data for phalangeal quantitative ultrasound from early childhood to young-adulthood according to gender, age, skeletal growth, and pubertal development.

M. Maghnie, G. Valerio, G. Saggese, 2006 .

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.

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

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

Cross-sectional reference data for phalangeal quantitative ultrasound from early childhood to young-adulthood according to gender, age, skeletal growth, and pubertal development.

M. Maghnie, G. Valerio, G. Saggese, 2006, Bone.

Mutations in the gene encoding thyroid transcription factor-1 (TTF-1) are not a frequent cause of congenital hypothyroidism (CH) with thyroid dysgenesis.

P. Macchia, D. Larizza, R. Lauro, 1997, Thyroid : official journal of the American Thyroid Association.

Risk factors for congenital hypothyroidism: results of a population case-control study (1997-2003).

V. Stoppioni, A. Pinchera, L. Chiovato, 2005, European journal of endocrinology.

Molecular characterization of six unrelated Italian patients affected by pyrimidine 5′‐nucleotidase deficiency

A. Zanella, P. Bianchi, B. Rotoli, 2003, British journal of haematology.

PAX8 mutations associated with congenital hypothyroidism caused by thyroid dysgenesis

Luca Chiovato, P. Macchia, R. Lauro, 1998, Nature Genetics.

Chromosomal instability in multiple endocrine neoplasia type 1. Cytogenetic evaluation with DEB test.

G. Paolucci, P. Tomassetti, M. Baserga, 1995, Cancer genetics and cytogenetics.

Congenital hypothyroidism in Calabria: epidemiological and clinical aspects.

M. Baserga, Mariateresa Pullano, 2009, Annali dell'Istituto superiore di sanita.