Capra V - Search Results

1

Moyamoya syndrome in children with neurofibromatosis type 1: Italian-French experience.

Santoro C, Di Rocco F, Kossorotoff M, Zerah M, Boddaert N, Calmon R, Vidaud D, Cirillo M, Cinalli G, Mirone G, Giugliano T, Piluso G, D'Amico A, Capra V, Pavanello M, Cama A, Nobili B, Lyonnet S, Perrotta S. Santoro C, et al. Among authors: capra v. Am J Med Genet A. 2017 Jun;173(6):1521-1530. doi: 10.1002/ajmg.a.38212. Epub 2017 Apr 19. Am J Med Genet A. 2017. PMID: 28422438

2

Germline mutations in the homeobox gene EMX2 in patients with severe schizencephaly.

Brunelli S, Faiella A, Capra V, Nigro V, Simeone A, Cama A, Boncinelli E. Brunelli S, et al. Among authors: capra v. Nat Genet. 1996 Jan;12(1):94-6. doi: 10.1038/ng0196-94. Nat Genet. 1996. PMID: 8528262 No abstract available.

3

Schizencephaly: surgical features and new molecular genetic results.

Capra V, De Marco P, Moroni A, Faiella A, Brunelli S, Tortori-Donati P, Andreussi I, Boncinelli E, Cama A. Capra V, et al. Eur J Pediatr Surg. 1996 Dec;6 Suppl 1:27-9. doi: 10.1055/s-2008-1071034. Eur J Pediatr Surg. 1996. PMID: 9008816

4

Multidisciplinary management of caudal regression syndrome (26 cases).

Cama A, Palmieri A, Capra V, Piatelli GL, Ravegnani M, Fondelli P. Cama A, et al. Among authors: capra v. Eur J Pediatr Surg. 1996 Dec;6 Suppl 1:44-5. Eur J Pediatr Surg. 1996. PMID: 9008829 No abstract available.

5

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.

6

Folate pathway gene alterations in patients with neural tube defects.

De Marco P, Moroni A, Merello E, de Franchis R, Andreussi L, Finnell RH, Barber RC, Cama A, Capra V. De Marco P, et al. Among authors: capra v. Am J Med Genet. 2000 Nov 27;95(3):216-23. doi: 10.1002/1096-8628(20001127)95:3<216::aid-ajmg6>3.0.co;2-f. Am J Med Genet. 2000. PMID: 11102926

7

Fontaine-Farriaux craniosynostosis: second report in the literature.

Priolo M, De Toni T, Baffico M, Cama A, Seri M, Cusano R, Costabello L, Fondelli P, Capra V, Silengo M, Ravazzolo R, Lerone M. Priolo M, et al. Among authors: capra v. Am J Med Genet. 2001 May 1;100(3):214-8. Am J Med Genet. 2001. PMID: 11343306

8

Polymorphisms in genes involved in folate metabolism as risk factors for NTDs.

De Marco P, Calevo MG, Moroni A, Arata L, Merello E, Cama A, Finnell RH, Andreussi L, Capra V. De Marco P, et al. Among authors: capra v. Eur J Pediatr Surg. 2001 Dec;11 Suppl 1:S14-7. doi: 10.1055/s-2001-19739. Eur J Pediatr Surg. 2001. PMID: 11813127

9

Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population.

De Marco P, Calevo MG, Moroni A, Arata L, Merello E, Finnell RH, Zhu H, Andreussi L, Cama A, Capra V. De Marco P, et al. Among authors: capra v. J Hum Genet. 2002;47(6):319-24. doi: 10.1007/s100380200043. J Hum Genet. 2002. PMID: 12111380

10

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

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