Merello E - Search Results

1

Urological outcome in patients with Currarino syndrome.

Pio L, Piatelli G, Rossi A, Scarsi P, Merello E, Capra V, Cama A, Buffa P, Torre M. Pio L, et al. Among authors: merello e. J Pediatr Surg. 2014 Nov;49(11):1643-6. doi: 10.1016/j.jpedsurg.2014.05.038. Epub 2014 Oct 31. J Pediatr Surg. 2014. PMID: 25475810

2

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. 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

3

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. 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

4

Planar cell polarity gene mutations contribute to the etiology of human neural tube defects in our population.

De Marco P, Merello E, Piatelli G, Cama A, Kibar Z, Capra V. De Marco P, et al. Among authors: merello e. Birth Defects Res A Clin Mol Teratol. 2014 Aug;100(8):633-41. doi: 10.1002/bdra.23255. Epub 2014 May 17. Birth Defects Res A Clin Mol Teratol. 2014. PMID: 24838524 Review.

5

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: merello e. 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

6

Leiomyomatosis peritonealis disseminata in association with Currarino syndrome?

Nappi C, Di Spiezio Sardo A, Mandato VD, Bifulco G, Merello E, Savanelli A, Mignogna C, Capra V, Guida M. Nappi C, et al. Among authors: merello e. BMC Cancer. 2006 May 10;6:127. doi: 10.1186/1471-2407-6-127. BMC Cancer. 2006. PMID: 16686944 Free PMC article.

7

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: merello e. 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

8

Maternal periconceptional factors affect the risk of spina bifida-affected pregnancies: an Italian case-control study.

De Marco P, Merello E, Calevo MG, Mascelli S, Pastorino D, Crocetti L, De Biasio P, Piatelli G, Cama A, Capra V. De Marco P, et al. Among authors: merello e. Childs Nerv Syst. 2011 Jul;27(7):1073-81. doi: 10.1007/s00381-010-1372-y. Epub 2011 Jan 5. Childs Nerv Syst. 2011. PMID: 21207040

9

Human neural tube defects: genetic causes and prevention.

De Marco P, Merello E, Cama A, Kibar Z, Capra V. De Marco P, et al. Among authors: merello e. Biofactors. 2011 Jul-Aug;37(4):261-8. doi: 10.1002/biof.170. Epub 2011 Jun 14. Biofactors. 2011. PMID: 21674647 Review.

10

FZD6 is a novel gene for human neural tube defects.

De Marco P, Merello E, Rossi A, Piatelli G, Cama A, Kibar Z, Capra V. De Marco P, et al. Among authors: merello e. Hum Mutat. 2012 Feb;33(2):384-90. doi: 10.1002/humu.21643. Epub 2011 Nov 28. Hum Mutat. 2012. PMID: 22045688 Free PMC article.

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