Optic Neuropathy AFG3L2 Related in a Patient Affected by Congenital Stationary Night Blindness.

Autor: Cammarata, Gabriella¹ (AUTHOR) g.cammarata@auxologico.it, Mihalich, Alessandra² (AUTHOR), Manfredini, Emanuela² (AUTHOR), Lamperti, Costanza³ (AUTHOR), Bianchi Marzoli, Stefania¹ (AUTHOR), Di Blasio, Anna Maria² (AUTHOR), Schwartz, Stephen G. (AUTHOR) sschwartz2@med.miami.edu

Publikováno v: Case Reports in Ophthalmological Medicine. 11/11/2024, Vol. 2024, p1-7. 7p.

Two novel CACNA1F gene mutations cause two different phenotypes: Aland Eye Disease and incomplete Congenital Stationary Night Blindness

Autor: Mihalich, Alessandra, Cammarata, Gabriella, Tremolada, Gemma, Pollazzon, Marzia, Di Blasio, Anna Maria, Marzoli, Stefania Bianchi

Publikováno v: In Experimental Eye Research August 2022 221

Physical map of the D6S149-D6S193 region on chromosome 6Q27 and its involement in benign surface epithelial ovarian tumours.

Autor: Tibiletti, Maria Grazia, Trubia, Maurizio, Ponti, Emanuela, Sessa, Luca, Acquati, Francesco, Furlan, Daniela, Bernasconi, Barbara, Fichera, Manuela, Mihalich, Alessandra, Ziegler, Andreas, Volz, Armin, Facco, Carla, Riva, Cristina, Cremonesi, Laura, Ferrari, Maurizio, Taramelli, Roberto

Publikováno v: Oncogene; 3/26/98, Vol. 16 Issue 12, p1639, 4p

Highly sensitive serum thyroglobulin and circulating thyroglobulin mRNA evaluations in the management of patients with differentiated thyroid cancer in apparent remission.

Autor: Fugazzola L; Institute of Endocrine Sciences, University of Milan, Ospedale Maggiore Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Via Franceses Sforza 35, Milan 20122, Italy., Mihalich A, Persani L, Cerutti N, Reina M, Bonomi M, Ponti E, Mannavola D, Giammona E, Vannucchi G, di Blasio AM, Beck-Peccoz P

Publikováno v: The Journal of clinical endocrinology and metabolism [J Clin Endocrinol Metab] 2002 Jul; Vol. 87 (7), pp. 3201-8.