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Von Hippel-Lindau disease and multispecialist team.
Pavesi G, Feletti A, Ferrara AM, Anglani M, Scarpa B, Schiavi F, Boaretto F, Zovato S, Taschin E, Gardi M, Zanoletti E, Piermarocchi S, Murgia A, Opocher G; VHL-Padova Network. Pavesi G, et al. Among authors: murgia a. J Neurosurg Sci. 2021 Apr;65(2):213-215. doi: 10.23736/S0390-5616.20.04950-4. Epub 2020 Apr 29. J Neurosurg Sci. 2021. PMID: 32347679 No abstract available.
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. Feletti A, et al. Among authors: murgia a. Neuro Oncol. 2016 Jul;18(7):1011-20. doi: 10.1093/neuonc/nov313. Epub 2016 Jan 12. Neuro Oncol. 2016. PMID: 26763786 Free PMC article.
Molecular diagnosis of von Hippel-Lindau disease.
Murgia A, Martella M, Polli R, Piermarocchi S, Lo Giudice G, Opocher G. Murgia A, et al. Contrib Nephrol. 2001;(136):263-70. doi: 10.1159/000060193. Contrib Nephrol. 2001. PMID: 11688392 No abstract available.
Somatic mosaicism in von Hippel-Lindau Disease.
Murgia A, Martella M, Vinanzi C, Polli R, Perilongo G, Opocher G. Murgia A, et al. Hum Mutat. 2000 Jan;15(1):114. doi: 10.1002/(SICI)1098-1004(200001)15:1<114::AID-HUMU20>3.0.CO;2-7. Hum Mutat. 2000. PMID: 10612832
Familial nonsyndromic pheochromocytoma.
Opocher G, Schiavi F, Iacobone M, Toniato A, Sattarova S, Erlic Z, Martella M, Mian C, Merante Boschin I, Zambonin L, De Lazzari P, Murgia A, Pelizzo MR, Favia G, Mantero F. Opocher G, et al. Among authors: murgia a. Ann N Y Acad Sci. 2006 Aug;1073:149-55. doi: 10.1196/annals.1353.015. Ann N Y Acad Sci. 2006. PMID: 17102081
Molecular diagnosis of inherited diseases.
Murgia A, Polli R, Martella M, Vinanzi C, Opocher G. Murgia A, et al. Clin Chim Acta. 1999 Feb;280(1-2):73-80. doi: 10.1016/s0009-8981(98)00199-5. Clin Chim Acta. 1999. PMID: 10090525 Review.
239 results