Capra V - Search Results

1

Novel MNX1 mutations and clinical analysis of familial and sporadic Currarino cases.

Merello E, De Marco P, Ravegnani M, Riccipetitoni G, Cama A, Capra V. Merello E, et al. Among authors: capra v. Eur J Med Genet. 2013 Dec;56(12):648-54. doi: 10.1016/j.ejmg.2013.09.011. Epub 2013 Oct 3. Eur J Med Genet. 2013. PMID: 24095820

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

A genetic polymorphism in the human HOXB1 homeobox gene implying a 9bp tandem repeat in the amino-terminal coding region. Mutations in brief no. 200. Online.

Faiella A, Zortea M, Barbaria E, Albani F, Capra V, Cama A, Boncinelli E. Faiella A, et al. Among authors: capra v. Hum Mutat. 1998;12(5):363. Hum Mutat. 1998. PMID: 10671062

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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