• 79 Citations
  • 4 h-Index
20162018
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Research Output 2016 2018

  • 79 Citations
  • 4 h-Index
  • 6 Article
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Article
2018

Paragangliomas arise through an autonomous vasculo-angio-neurogenic program inhibited by imatinib

Verginelli, F., Perconti, S., Vespa, S., Schiavi, F., Prasad, S. C., Lanuti, P., Cama, A., Tramontana, L., Esposito, D. L., Guarnieri, S., Sheu, A., Pantalone, M. R., Florio, R., Morgano, A., Rossi, C., Bologna, G., Marchisio, M., D'Argenio, A., Taschin, E., Visone, R. & 8 others, Opocher, G., Veronese, A., Paties, C. T., Rajasekhar, V. K., Söderberg-Nauclér, C., Sanna, M., Lotti, L. V. & Mariani-Costantini, R., May 2018, In : Acta Neuropathologica. 135, 5, p. 779-798 20 p.

Research output: Contribution to journalArticle

Paraganglioma
Heterografts
Stem Cells
Organoids
Choristoma
2017

A multicenter experience on the prevalence of ARMC5 mutations in patients with primary bilateral macronodular adrenal hyperplasia: from genetic characterization to clinical phenotype

Albiger, N. M., Regazzo, D., Rubin, B., Ferrara, A. M., Rizzati, S., Taschin, E., Ceccato, F., Arnaldi, G., Pecori Giraldi, F., Stigliano, A., Cerquetti, L., Grimaldi, F., De Menis, E., Boscaro, M., Iacobone, M., Occhi, G. & Scaroni, C., Mar 2017, In : Endocrine. 55, 3, p. 959-968 10 p.

Research output: Contribution to journalArticle

Hyperplasia
Phenotype
Mutation
Hydrocortisone
Germ-Line Mutation
18 Citations (Scopus)

A multicenter experience on the prevalence of ARMC5 mutations in patients with primary bilateral macronodular adrenal hyperplasia: from genetic characterization to clinical phenotype

Albiger, N. M., Regazzo, D., Rubin, B., Ferrara, A. M., Rizzati, S., Taschin, E., Ceccato, F., Arnaldi, G., Pecori Giraldi, F., Stigliano, A., Cerquetti, L., Grimaldi, F., De Menis, E., Boscaro, M., Iacobone, M., Occhi, G. & Scaroni, C., 2017, In : Endocrine. 55, 3, p. 959-968 10 p.

Research output: Contribution to journalArticle

47 Citations (Scopus)

Clinical characterization of the pheochromocytoma and paraganglioma susceptibility genes SDHA, TMEM127, MAX, and SDHAF2 for gene-informed prevention

Bausch, B., Schiavi, F., Ni, Y., Welander, J., Patocs, A., Ngeow, J., Wellner, U., Malinoc, A., Taschin, E., Barbon, G., Lanza, V., Söderkvist, P., Stenman, A., Larsson, C., Svahn, F., Chen, J. L., Marquard, J., Fraenkel, M., Walter, M. A., Peczkowska, M. & 25 others, Prejbisz, A., Jarzab, B., Hasse-Lazar, K., Petersenn, S., Moeller, L. C., Meyer, A., Reisch, N., Trupka, A., Brase, C., Galiano, M., Preuss, S. F., Kwok, P., Lendvai, N., Berisha, G., Makay, Ö., Boedeker, C. C., Weryha, G., Racz, K., Januszewicz, A., Walz, M. K., Gimm, O., Opocher, G., Eng, C., Neumann, H. P. H. & European-American-Asian Pheochromocytoma-Paraganglioma Registry Study Group, Sep 1 2017, In : JAMA oncology. 3, 9, p. 1204-1212 9 p.

Research output: Contribution to journalArticle

Paraganglioma
Pheochromocytoma
Mutation
Germ-Line Mutation
Genes
2016
4 Citations (Scopus)

First steps to define murine amniotic fluid stem cell microenvironment

Bertin, E., Piccoli, M., Franzin, C., Spiro, G., Donà, S., Dedja, A., Schiavi, F., Taschin, E., Bonaldo, P., Braghetta, P., De Coppi, P. & Pozzobon, M., Nov 15 2016, In : Scientific Reports. 6, 37080.

Research output: Contribution to journalArticle

Stem Cell Niche
Amniotic Fluid
Embryonic Stem Cells
Amnion
Stem Cells
10 Citations (Scopus)

Von Hippel-Lindau disease: An evaluation of natural history and functional disability

Feletti, A., Anglani, M., Scarpa, B., Schiavi, F., Boaretto, F., Zovato, S., Taschin, E., Gardi, M., Zanoletti, E., Piermarocchi, S., Murgia, A., Pavesi, G. & Opocher, G., Jul 1 2016, In : Neuro-Oncology. 18, 7, p. 1011-1020 10 p.

Research output: Contribution to journalArticle

von Hippel-Lindau Disease
Natural History
Hemangioblastoma
Mutation
Kidney Neoplasms