Lerone M - Search Results

1

Association of multiple endocrine neoplasia type 2 and Hirschsprung disease.

Romeo G, Ceccherini I, Celli J, Priolo M, Betsos N, Bonardi G, Seri M, Yin L, Lerone M, Jasonni V, Martucciello G. Romeo G, et al. Among authors: lerone m. J Intern Med. 1998 Jun;243(6):515-20. doi: 10.1046/j.1365-2796.1998.00332.x. J Intern Med. 1998. PMID: 9681852 Free article.

2

Pathogenesis of Hirschsprung's disease.

Martucciello G, Ceccherini I, Lerone M, Jasonni V. Martucciello G, et al. Among authors: lerone m. J Pediatr Surg. 2000 Jul;35(7):1017-25. doi: 10.1053/jpsu.2000.7763. J Pediatr Surg. 2000. PMID: 10917288 Review.

3

Diagnostic and therapeutic approach to multiple endocrine neoplasia type 2B in pediatric patients.

Torre M, Martucciello G, Ceccherini I, Lerone M, Aicardi M, Gambini C, Jasonni V. Torre M, et al. Among authors: lerone m. Pediatr Surg Int. 2002 Sep;18(5-6):378-83. doi: 10.1007/s00383-002-0824-1. Epub 2002 Apr 11. Pediatr Surg Int. 2002. PMID: 12415360

4

Heterogeneity and low detection rate of RET mutations in Hirschsprung disease.

Yin L, Barone V, Seri M, Bolino A, Bocciardi R, Ceccherini I, Pasini B, Tocco T, Lerone M, Cywes S, et al. Yin L, et al. Among authors: lerone m. Eur J Hum Genet. 1994;2(4):272-80. doi: 10.1159/000472371. Eur J Hum Genet. 1994. PMID: 7704557

5

Point mutations affecting the tyrosine kinase domain of the RET proto-oncogene in Hirschsprung's disease.

Romeo G, Ronchetto P, Luo Y, Barone V, Seri M, Ceccherini I, Pasini B, Bocciardi R, Lerone M, Kääriäinen H, et al. Romeo G, et al. Among authors: lerone m. Nature. 1994 Jan 27;367(6461):377-8. doi: 10.1038/367377a0. Nature. 1994. PMID: 8114938

6

Deleted and normal chromosome 10 homologs from a patient with Hirschsprung disease isolated in two cell hybrids through enrichment by immunomagnetic selection.

Puliti A, Covone AE, Bicocchi MP, Bolino A, Lerone M, Martucciello G, Jasonni V, Romeo G. Puliti A, et al. Among authors: lerone m. Cytogenet Cell Genet. 1993;63(2):102-6. doi: 10.1159/000133510. Cytogenet Cell Genet. 1993. PMID: 8467706

7

Frequency of RET mutations in long- and short-segment Hirschsprung disease.

Seri M, Yin L, Barone V, Bolino A, Celli I, Bocciardi R, Pasini B, Ceccherini I, Lerone M, Kristoffersson U, Larsson LT, Casasa JM, Cass DT, Abramowicz MJ, Vanderwinden JM, Kravcenkiene I, Baric I, Silengo M, Martucciello G, Romeo G. Seri M, et al. Among authors: lerone m. Hum Mutat. 1997;9(3):243-9. doi: 10.1002/(SICI)1098-1004(1997)9:3<243::AID-HUMU5>3.0.CO;2-8. Hum Mutat. 1997. PMID: 9090527

8

Search for pathogenetic variants of the SPRY2 gene in intestinal innervation defects.

Borghini S, Duca MD, Pini Prato A, Lerone M, Martucciello G, Jasonni V, Ravazzolo R, Ceccherini I. Borghini S, et al. Among authors: lerone m. Intern Med J. 2009 May;39(5):335-7. doi: 10.1111/j.1445-5994.2009.01907.x. Intern Med J. 2009. PMID: 19545245

9

The genetics of anorectal malformations: a complex matter.

Lerone M, Bolino A, Martucciello G. Lerone M, et al. Semin Pediatr Surg. 1997 Nov;6(4):170-9. Semin Pediatr Surg. 1997. PMID: 9368268 Review.

10

Currarino syndrome: proposal of a diagnostic and therapeutic protocol.

Martucciello G, Torre M, Belloni E, Lerone M, Pini Prato A, Cama A, Jasonni V. Martucciello G, et al. Among authors: lerone m. J Pediatr Surg. 2004 Sep;39(9):1305-11. doi: 10.1016/j.jpedsurg.2004.05.003. J Pediatr Surg. 2004. PMID: 15359381 Review.

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