Capra V - Search Results

1

Moyamoya Vasculopathy in PHACE Syndrome: Six New Cases and Review of the Literature.

Tortora D, Severino M, Accogli A, Martinetti C, Vercellino N, Capra V, Rossi A, Pavanello M. Tortora D, et al. Among authors: capra v. World Neurosurg. 2017 Dec;108:291-302. doi: 10.1016/j.wneu.2017.08.176. Epub 2017 Sep 5. World Neurosurg. 2017. PMID: 28887276 Review.

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

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

4

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

5

No major role for the EMX2 gene in schizencephaly.

Merello E, Swanson E, De Marco P, Akhter M, Striano P, Rossi A, Cama A, Leventer RJ, Guerrini R, Capra V, Dobyns WB. Merello E, et al. Among authors: capra v. Am J Med Genet A. 2008 May 1;146A(9):1142-50. doi: 10.1002/ajmg.a.32264. Am J Med Genet A. 2008. PMID: 18409201

6

Craniosynostosis, hydrocephalus, Chiari I malformation and radioulnar synostosis: probably a new syndrome.

Capra V, De Marco P, Merello E, Baffico AM, Baldi M, Divizia MT, Gimelli S, Mallet D, Raso A, Mascelli S, Tomà P, Rossi A, Pavanello M, Cama A, Magnani C. Capra V, et al. Eur J Med Genet. 2009 Jan-Feb;52(1):17-22. doi: 10.1016/j.ejmg.2008.10.005. Epub 2008 Nov 6. Eur J Med Genet. 2009. PMID: 19022412

7

Medulloblastoma variants: age-dependent occurrence and relation to Gorlin syndrome--a new clinical perspective.

Garrè ML, Cama A, Bagnasco F, Morana G, Giangaspero F, Brisigotti M, Gambini C, Forni M, Rossi A, Haupt R, Nozza P, Barra S, Piatelli G, Viglizzo G, Capra V, Bruno W, Pastorino L, Massimino M, Tumolo M, Fidani P, Dallorso S, Schumacher RF, Milanaccio C, Pietsch T. Garrè ML, et al. Among authors: capra v. Clin Cancer Res. 2009 Apr 1;15(7):2463-71. doi: 10.1158/1078-0432.CCR-08-2023. Epub 2009 Mar 10. Clin Cancer Res. 2009. PMID: 19276247

8

Treatment and outcome of children with cerebral cavernomas: a survey on 32 patients.

Consales A, Piatelli G, Ravegnani M, Pavanello M, Striano P, Zoli ML, Capra V, Rossi A, Garrè ML, Calevo MG, Cama A. Consales A, et al. Among authors: capra v. Neurol Sci. 2010 Apr;31(2):117-23. doi: 10.1007/s10072-009-0157-0. Epub 2009 Oct 16. Neurol Sci. 2010. PMID: 19834644

9

High levels of PROM1 (CD133) transcript are a potential predictor of poor prognosis in medulloblastoma.

Raso A, Mascelli S, Biassoni R, Nozza P, Kool M, Pistorio A, Ugolotti E, Milanaccio C, Pignatelli S, Ferraro M, Pavanello M, Ravegnani M, Cama A, Garrè ML, Capra V. Raso A, et al. Among authors: capra v. Neuro Oncol. 2011 May;13(5):500-8. doi: 10.1093/neuonc/nor022. Epub 2011 Apr 12. Neuro Oncol. 2011. PMID: 21486962 Free PMC article.

10

A de novo balanced translocation t(7;12)(p21.2;p12.3) in a patient with Saethre-Chotzen-like phenotype downregulates TWIST and an osteoclastic protein-tyrosine phosphatase, PTP-oc.

De Marco P, Raso A, Beri S, Gimelli S, Merello E, Mascelli S, Baldi M, Baffico AM, Pavanello M, Cama A, Capra V, Giorda R, Gimelli G. De Marco P, et al. Among authors: capra v. Eur J Med Genet. 2011 Sep-Oct;54(5):e478-83. doi: 10.1016/j.ejmg.2011.05.007. Epub 2011 Jun 25. Eur J Med Genet. 2011. PMID: 21708297

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