Publications: Miss Angelica Gualtieri
Giri D, Vignola ML, Gualtieri A, Scagliotti V, McNamara P, Peak M, Didi M, Gaston-Massuet C et al.(2017).
Novel FOXA2 mutation causes Hyperinsulinism, Hypopituitarism with Craniofacial and Endodermderived organ abnormalities. Human Molecular Genetics
vol. 26,
(22)
4315-4326.
Gaston-Massuet C, McCabe MJ, Scagliotti V, Young RM, Carreno G, Gregory LC, Jayakody SA, Pozzi S et al.(2016).
Transcription factor 7-like 1 is involved in hypothalamo-pituitary axis development in mice and humans. Proceedings of the National Academy of Sciences of the United States of America
vol. 113,
(5)
E548-E557.
Avagliano L, Doi P, Tosi D, Scagliotti V, Gualtieri A, Gaston-Massuet C, Pistocchi A, Gallina A et al.(2016).
Cell death and cell proliferation in human spina bifida. Birth Defects Research Part A - Clinical and Molecular Teratology
vol. 106,
(2)
104-113.
Scagliotti V, Avagliano L, Gualtieri A, Graziola F, Doi P, Chalker J, Righini A, Korbonits M et al.(2016).
Histopathology and molecular characterisation of intrauterine-diagnosed congenital craniopharyngioma. Pituitary
vol. 19,
(1)
50-56.
McCabe MJ, Hu Y, Gregory LC, Gaston-Massuet C, Alatzoglou KS, Saldanha JW, Gualtieri A, Thankamony A et al.(2015).
Novel application of luciferase assay for the in vitro functional assessment of KAL1 variants in three females with septo-optic dysplasia (SOD). Molecular and Cellular Endocrinology
vol. 417,
63-72.