Capra V - Search Results

1

De novo MGC4607 gene heterozygous missense variants in a child with multiple cerebral cavernous malformations.

Mosca L, Pileggi S, Avemaria F, Tarlarini C, Cigoli MS, Capra V, De Marco P, Pavanello M, Marocchi A, Penco S. Mosca L, et al. Among authors: capra v. J Mol Neurosci. 2012 Jul;47(3):475-80. doi: 10.1007/s12031-012-9741-5. Epub 2012 Mar 14. J Mol Neurosci. 2012. PMID: 22415356

2

Molecular genetic analysis of human homologs of Caenorhabditis elegans mab-21-like 1 gene in patients with neural tube defects.

Merello E, De Marco P, Moroni A, Raso A, Calevo MG, Consalez GG, Cama A, Capra V. Merello E, et al. Among authors: capra v. Birth Defects Res A Clin Mol Teratol. 2004 Nov;70(11):885-8. doi: 10.1002/bdra.20084. Birth Defects Res A Clin Mol Teratol. 2004. PMID: 15526290

3

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

4

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

5

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

6

Current perspectives on the genetic causes of neural tube defects.

De Marco P, Merello E, Mascelli S, Capra V. De Marco P, et al. Among authors: capra v. Neurogenetics. 2006 Nov;7(4):201-21. doi: 10.1007/s10048-006-0052-2. Epub 2006 Aug 29. Neurogenetics. 2006. PMID: 16941185 Review.

7

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

8

Mutations in VANGL1 associated with neural-tube defects.

Kibar Z, Torban E, McDearmid JR, Reynolds A, Berghout J, Mathieu M, Kirillova I, De Marco P, Merello E, Hayes JM, Wallingford JB, Drapeau P, Capra V, Gros P. Kibar Z, et al. Among authors: capra v. N Engl J Med. 2007 Apr 5;356(14):1432-7. doi: 10.1056/NEJMoa060651. N Engl J Med. 2007. PMID: 17409324 Free article.

9

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

10

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

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