Martella M - Search Results

1

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: martella m. Ann N Y Acad Sci. 2006 Aug;1073:149-55. doi: 10.1196/annals.1353.015. Ann N Y Acad Sci. 2006. PMID: 17102081

2

Fine analysis of the short arm of chromosome 1 in sporadic and familial pheochromocytoma.

Opocher G, Schiavi F, Vettori A, Pampinella F, Vitiello L, Calderan A, Vianello B, Murgia A, Martella M, Taccaliti A, Mantero F, Mostacciuolo ML. Opocher G, et al. Among authors: martella m. Clin Endocrinol (Oxf). 2003 Dec;59(6):707-15. doi: 10.1046/j.1365-2265.2003.01910.x. Clin Endocrinol (Oxf). 2003. PMID: 14974911

3

Molecular analysis of two uncharacterized sequence variants of the VHL gene.

Martella M, Salviati L, Casarin A, Trevisson E, Opocher G, Polli R, Gross D, Murgia A. Martella M, et al. J Hum Genet. 2006;51(11):964-968. doi: 10.1007/s10038-006-0054-9. Epub 2006 Sep 28. J Hum Genet. 2006. PMID: 17006605

4

Molecular characterization of large deletions in the von Hippel-Lindau (VHL) gene by quantitative real-time PCR: the hypothesis of an alu-mediated mechanism underlying VHL gene rearrangements.

Casarin A, Martella M, Polli R, Leonardi E, Anesi L, Murgia A. Casarin A, et al. Among authors: martella m. Mol Diagn Ther. 2006;10(4):243-9. doi: 10.1007/BF03256463. Mol Diagn Ther. 2006. PMID: 16884328

5

Identification and in silico analysis of novel von Hippel-Lindau (VHL) gene variants from a large population.

Leonardi E, Martella M, Tosatto SC, Murgia A. Leonardi E, et al. Among authors: martella m. Ann Hum Genet. 2011 Jul;75(4):483-96. doi: 10.1111/j.1469-1809.2011.00647.x. Epub 2011 Apr 4. Ann Hum Genet. 2011. PMID: 21463266

6

Somatic mosaicism in von Hippel-Lindau Disease.

Murgia A, Martella M, Vinanzi C, Polli R, Perilongo G, Opocher G. Murgia A, et al. Among authors: martella m. 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

7

Neurosurgical treatment of von Hippel-Lindau-associated hemangioblastomas: benefits, risks and outcome.

Pavesi G, Feletti A, Berlucchi S, Opocher G, Martella M, Murgia A, Scienza R. Pavesi G, et al. Among authors: martella m. J Neurosurg Sci. 2008 Jun;52(2):29-36. J Neurosurg Sci. 2008. PMID: 18500215

8

Low frequency of VHL gene mutations in young individuals with polycythemia and high serum erythropoietin.

Randi ML, Murgia A, Putti MC, Martella M, Casarin A, Opocher G, Fabris F. Randi ML, et al. Among authors: martella m. Haematologica. 2005 May;90(5):689-91. Haematologica. 2005. PMID: 15921386

9

Molecular diagnosis of inherited diseases.

Murgia A, Polli R, Martella M, Vinanzi C, Opocher G. Murgia A, et al. Among authors: martella m. 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.

10

Retinal abnormalities associated with a mutation of the nucleotide 683 in von Hippel-Lindau disease.

Piermarocchi S, Lo Giudice G, Pilotto E, Bertoja E, Scaroni C, Martella M, Opocher G, Murgia A. Piermarocchi S, et al. Among authors: martella m. Graefes Arch Clin Exp Ophthalmol. 2000 Jul;238(7):615-20. doi: 10.1007/s004170000129. Graefes Arch Clin Exp Ophthalmol. 2000. PMID: 10955664

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

98 results

Search Page