Capra V - Search Results

1

Genetic abnormalities and CNS tumors: report of two cases of ependymoma associated with Klinefelter's Syndrome (KS).

Garrè ML, Capra V, Di Battista E, Giampietri L, Nozza P, Raso A, Pezzolo A, Rossi A, Milanaccio C, Pavanello M, Naselli A. Garrè ML, et al. Among authors: capra v. Childs Nerv Syst. 2007 Feb;23(2):219-23. doi: 10.1007/s00381-006-0179-3. Epub 2006 Oct 13. Childs Nerv Syst. 2007. PMID: 17058088

2

Segmental spinal dysgenesis: neuroradiologic findings with clinical and embryologic correlation.

Tortori-Donati P, Fondelli MP, Rossi A, Raybaud CA, Cama A, Capra V. Tortori-Donati P, et al. Among authors: capra v. AJNR Am J Neuroradiol. 1999 Mar;20(3):445-56. AJNR Am J Neuroradiol. 1999. PMID: 10219410 Free PMC article.

3

Reduced folate carrier polymorphism (80A-->G) and neural tube defects.

De Marco P, Calevo MG, Moroni A, Merello E, Raso A, Finnell RH, Zhu H, Andreussi L, Cama A, Capra V. De Marco P, et al. Among authors: capra v. Eur J Hum Genet. 2003 Mar;11(3):245-52. doi: 10.1038/sj.ejhg.5200946. Eur J Hum Genet. 2003. PMID: 12673279

4

Rhabdoid meningioma of the tentorium with expression of desmin in a 12-year-old Turner syndrome patient.

Nozza P, Raso A, Rossi A, Milanaccio C, Pezzolo A, Capra V, Gambini C, Pietsch T. Nozza P, et al. Among authors: capra v. Acta Neuropathol. 2005 Aug;110(2):205-6. doi: 10.1007/s00401-005-1048-y. Epub 2005 Jul 16. Acta Neuropathol. 2005. PMID: 16025286 No abstract available.

5

Evaluation of a methylenetetrahydrofolate-dehydrogenase 1958G>A polymorphism for neural tube defect risk.

De Marco P, Merello E, Calevo MG, Mascelli S, Raso A, Cama A, Capra V. De Marco P, et al. Among authors: capra v. J Hum Genet. 2006;51(2):98-103. doi: 10.1007/s10038-005-0329-6. Epub 2005 Nov 29. J Hum Genet. 2006. PMID: 16315005

6

Mutational screening of the CYP26A1 gene in patients with caudal regression syndrome.

De Marco P, Merello E, Mascelli S, Raso A, Santamaria A, Ottaviano C, Calevo MG, Cama A, Capra V. De Marco P, et al. Among authors: capra v. Birth Defects Res A Clin Mol Teratol. 2006 Feb;76(2):86-95. doi: 10.1002/bdra.20225. Birth Defects Res A Clin Mol Teratol. 2006. PMID: 16463413

7

HLXB9 homeobox gene and caudal regression syndrome.

Merello E, De Marco P, Mascelli S, Raso A, Calevo MG, Torre M, Cama A, Lerone M, Martucciello G, Capra V. Merello E, et al. Among authors: capra v. Birth Defects Res A Clin Mol Teratol. 2006 Mar;76(3):205-9. doi: 10.1002/bdra.20234. Birth Defects Res A Clin Mol Teratol. 2006. PMID: 16498628

8

Brainstem anomalies in two patients affected by congenital central hypoventilation syndrome.

Bachetti T, Robbiano A, Parodi S, Matera I, Merello E, Capra V, Baglietto MP, Rossi A, Ceccherini I, Ottonello G. Bachetti T, et al. Among authors: capra v. Am J Respir Crit Care Med. 2006 Sep 15;174(6):706-9. doi: 10.1164/rccm.200602-266CR. Epub 2006 Jun 8. Am J Respir Crit Care Med. 2006. PMID: 16763219

9

Successful isolation and long-term establishment of a cell line with stem cell-like features from an anaplastic medulloblastoma.

Raso A, Negri F, Gregorio A, Nozza P, Mascelli S, De Marco P, Merello E, Milanaccio C, Ravegnani M, Cama A, Garrè ML, Capra V. Raso A, et al. Among authors: capra v. Neuropathol Appl Neurobiol. 2008 Jun;34(3):306-15. doi: 10.1111/j.1365-2990.2007.00896.x. Epub 2007 Nov 9. Neuropathol Appl Neurobiol. 2008. PMID: 17995922

10

Identification of novel chromosomal abnormalities and prognostic cytogenetics markers in intracranial pediatric ependymoma.

Pezzolo A, Capra V, Raso A, Morandi F, Parodi F, Gambini C, Nozza P, Giangaspero F, Cama A, Pistoia V, Garrè ML. Pezzolo A, et al. Among authors: capra v. Cancer Lett. 2008 Mar 18;261(2):235-43. doi: 10.1016/j.canlet.2007.11.021. Epub 2008 Jan 7. Cancer Lett. 2008. PMID: 18179864

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