Medullary Thyroid Carcinoma With Exon 2 p.L56M RET Variant: Clinical Particular Features in Two Patients
Paragliola, Rosa M, Lovicu, Rosa M, Papi, Giampaolo, Capoluongo, Ettore, Minucci, Angelo, Canu, Giulia, Pontecorvi, Alfredo, Corsello, Salvatore M
Published in Frontiers in endocrinology (Lausanne) (19.07.2018)
Published in Frontiers in endocrinology (Lausanne) (19.07.2018)
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Giant prolactinomas in men: efficacy of cabergoline treatment
Corsello, S. M., Ubertini, G., Altomare, M., Lovicu, R. M., Migneco, M. G., Rota, C. A., Colosimo, C.
Published in Clinical endocrinology (Oxford) (01.05.2003)
Published in Clinical endocrinology (Oxford) (01.05.2003)
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Long-term results of treatment in patients with ACTH-secreting pituitary macroadenomas
CANNAVO, S, ALMOTO, B, D'ALLASTA, C, CORSELLO, S, LOVICU, R. M, DE MENIS, E, TRIMARCHI, F, AMBROSI, B
Published in European journal of endocrinology (01.09.2003)
Published in European journal of endocrinology (01.09.2003)
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Mutation analysis in patients of Mediterranean descent with Wilson disease: identification of 19 novel mutations
Loudianos, Georgios, Dessi, Valeria, Lovicu, Mario, Angius, Andrea, Altuntas, Buket, Giacchino, Raffaella, Marazzi, Maria, Marcellini, Matilde, Sartorelli, Maria Rita, Sturniolo, Giacomo Carlo, Kocak, Nurten, Yuce, Aysel, Akar, Nejat, Pirastu, Mario, Cao, Antonio
Published in Journal of medical genetics (01.11.1999)
Published in Journal of medical genetics (01.11.1999)
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Abnormal mRNA splicing resulting from consensus sequence splicing mutations of ATP7B
Loudianos, G., Lovicu, M., Dessi, V., Tzetis, M., Kanavakis, E., Zancan, L., Zelante, L., Galvèz-Galvèz, C., Cao, A.
Published in Human mutation (01.10.2002)
Published in Human mutation (01.10.2002)
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Levothyroxine therapy in preventing nodular recurrence after hemithyroidectomy: A retrospective study
Alba, M., Fintini, D., Lovicu, R. M., Paragliola, R. M., Papi, G., Rota, C. A., Pontecorvi, A., Corsello, S. M.
Published in Journal of endocrinological investigation (01.04.2009)
Published in Journal of endocrinological investigation (01.04.2009)
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Direct Diagnosis of Wilson Disease by Molecular Genetics
Caprai, Silvia, Loudianos, Georgios, Massei, Francesco, Gori, Laura, Lovicu, Mario, Maggiore, Giuseppe
Published in The Journal of pediatrics (2006)
Published in The Journal of pediatrics (2006)
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Molecular characterization of Wilson disease in the Sardinian population-Evidence of a founder effect
Loudianos, Georgios, Dessi, Valeria, Lovicu, Mario, Angius, Andrea, Figus, Annalena, Lilliu, Franco, De Virgiliis, Stefano, Nurchi, Anna Maria, Deplano, Angelo, Moi, Paolo, Pirastu, Mario, Cao, Antonio
Published in Human mutation (01.01.1999)
Published in Human mutation (01.01.1999)
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G-6-PD Cagliari II: a new G-6-PD variant
Frigerio, R, Sole, G, Olla, N, Lovicu, M, Passiu, G, Carcassi, U
Published in Haematologica (Roma) (01.05.1987)
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Published in Haematologica (Roma) (01.05.1987)
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Twenty-four novel mutations in Wilson disease patients of predominantly Italian origin
Lepori, Maria Barbara, Lovicu, Mario, Dessi, Valentina, Zappu, Antonietta, Incollu, Simona, Zancan, Lucia, Giacchino, Raffaella, Iorio, Raffaele, Vajro, Pietro, Maggiore, Giuseppe, Marcellini, Matilde, Barbera, Cristiana, Pellecchia, Maria Teresa, Simonetti, Rosanna, Kostic, Vladimir, Farci, Anna Maria Giulia, Solinas, Antonello, De Virgiliis, Stefano, Cao, Antonio, Loudianos, Georgios
Published in Genetic testing (01.09.2007)
Published in Genetic testing (01.09.2007)
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Journal Article
Delineation of the spectrum of Wilson disease mutations in the Greek population and the identification of six novel mutations
Loudianos, G, Lovicu, M, Solinas, P, Kanavakis, E, Tzetis, M, Manolaki, N, Panagiotakaki, E, Karpathios, T, Cao, A
Published in Genetic testing (2000)
Published in Genetic testing (2000)
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Journal Article
RNA analysis of consensus sequence splicing mutations: implications for the diagnosis of Wilson disease
Lovicu, Mario, Lepori, Maria Barbara, Incollu, Simona, Dessì, Valentina, Zappu, Antonietta, Iorio, Raffaele, D'Ambrosi, Mariangela, Pellecchia, Maria Teresa, Barone, Paolo, Maggiore, Giuseppe, De Virgiliis, Stefano, Cao, Antonio, Loudianos, Georgios
Published in Genetic testing and molecular biomarkers (01.04.2009)
Published in Genetic testing and molecular biomarkers (01.04.2009)
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Molecular pathology and haplotype analysis of Wilson disease in Mediterranean populations
FIGUS, A, ANGIUS, A, DE VIRGILIIS, S, LILLIU, F, FARCI, A. M. G, NURCHI, A, GIACCHINO, R, BARABINO, A, MARAZZI, M, ZANCAN, L, GREGGIO, N. A, MARCELLINI, M, LOUDIANOS, G, SOLINAS, A, DEPLANO, A, BARBERA, C, DEVOTO, M, OZSOYLU, S, KOCAK, N, AKAR, N, KARAYALCIN, S, MOKINI, V, CULLUFI, P, BERTINI, C, BALESTRIERI, A, CAO, A, PIRASTU, M, DESSI, V, LOI, A, DEIANA, M, LOVICU, M, OLLA, N, SOLE, G
Published in American journal of human genetics (01.12.1995)
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Published in American journal of human genetics (01.12.1995)
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Further delineation of the molecular pathology of Wilson disease in the Mediterranean population
Loudianos, Georgios, Dessì, Valeria, Lovicu, Mario, Angius, Andrea, Nurchi, Annamaria, Sturniolo, Giacomo Carlo, Marcellini, Matilde, Zancan, Lucia, Bragetti, Patrizia, Akar, Nejat, Yagci, Rasit, Vegnente, Angela, Cao, Antonio, Pirastu, Mario
Published in Human mutation (1998)
Published in Human mutation (1998)
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P0189 THE CANINE COPPER TOXICOSIS GENE MURR1 IS NOT IMPLICATED IN THE PATHOGENESIS OF WILSON DISEASE
Loudianos, G., Lovicu, M., Dessì, V., Altuntas, B., Vegnente, A., Farci, M., Solinas, A., De Virgiliis, S., Cao, A.
Published in Journal of pediatric gastroenterology and nutrition (01.06.2004)
Published in Journal of pediatric gastroenterology and nutrition (01.06.2004)
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Journal Article
P0189 THE CANINE COPPER TOXICOSIS GENE MURR1 IS NOT IMPLICATED IN THE PATHOGENESIS OF WILSON DISEASE
Loudianos, G., Lovicu, M., Dess??, V., Altuntas, B., Vegnente, A., Farci, M., Solinas, A., De Virgiliis, S., Cao, A.
Published in Journal of pediatric gastroenterology and nutrition (01.06.2004)
Published in Journal of pediatric gastroenterology and nutrition (01.06.2004)
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Detection of a rare Wilson disease mutation associated with arylsulfatase A pseudodeficiency
Battisti, C, Loudianos, G, Rufa, A, Dotti, M T, Sangiorgi, S, Dessì, V, Lovicu, M, Pirastu, M, Federico, A
Published in American journal of medical genetics (16.07.1999)
Published in American journal of medical genetics (16.07.1999)
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