Capra V - Search Results

1

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

2

Cytogenetics of the tissue involved in neural tube defects.

Haupt R, Byrne J, Defferrari R, Cama A, Levato L, Lavia N, Vigliarolo MA, Capra V, Andreussi L. Haupt R, et al. Among authors: capra v. Genet Couns. 1995;6(1):49-53. Genet Couns. 1995. PMID: 7794562

3

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.

4

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

5

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.

6

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.

7

Pfeiffer syndrome type 2 associated with a single amino acid deletion in the FGFR2 gene.

Priolo M, Lerone M, Baffico M, Baldi M, Ravazzolo R, Cama A, Capra V, Silengo M. Priolo M, et al. Among authors: capra v. Clin Genet. 2000 Jul;58(1):81-3. doi: 10.1034/j.1399-0004.2000.580116.x. Clin Genet. 2000. PMID: 10945669 No abstract available.

8

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

9

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

10

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

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