Romeo G - Search Results

1

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: romeo g. 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

2

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. Nature. 1994 Jan 27;367(6461):377-8. doi: 10.1038/367377a0. Nature. 1994. PMID: 8114938

3

Interstitial deletion of the endothelin-B receptor gene in the spotting lethal (sl) rat.

Ceccherini I, Zhang AL, Matera I, Yang G, Devoto M, Romeo G, Cass DT. Ceccherini I, et al. Among authors: romeo g. Hum Mol Genet. 1995 Nov;4(11):2089-96. doi: 10.1093/hmg/4.11.2089. Hum Mol Genet. 1995. PMID: 8589685

4

RET mutations in human disease.

Pasini B, Ceccherini I, Romeo G. Pasini B, et al. Among authors: romeo g. Trends Genet. 1996 Apr;12(4):138-44. doi: 10.1016/0168-9525(96)10012-3. Trends Genet. 1996. PMID: 8901418 Review.

5

Prevalence and parental origin of de novo RET mutations in Hirschsprung's disease.

Yin L, Seri M, Barone V, Tocco T, Scaranari M, Romeo G. Yin L, et al. Among authors: romeo g. Eur J Hum Genet. 1996;4(6):356-8. doi: 10.1159/000472232. Eur J Hum Genet. 1996. PMID: 9043870

6

Startle disease in an Italian family by mutation (K276E): The alpha-subunit of the inhibiting glycine receptor.

Seri M, Bolino A, Galietta LJ, Lerone M, Silengo M, Romeo G. Seri M, et al. Among authors: romeo g. Hum Mutat. 1997;9(2):185-7. doi: 10.1002/(SICI)1098-1004(1997)9:2<185::AID-HUMU14>3.0.CO;2-Z. Hum Mutat. 1997. PMID: 9067762 No abstract available.

7

A Cys634Gly substitution of the RET proto-oncogene in a family with recurrence of multiple endocrine neoplasia type 2A and cutaneous lichen amyloidosis.

Seri M, Celli I, Betsos N, Claudiani F, Camera G, Romeo G. Seri M, et al. Among authors: romeo g. Clin Genet. 1997 Feb;51(2):86-90. doi: 10.1111/j.1399-0004.1997.tb02425.x. Clin Genet. 1997. PMID: 9111993

8

A single-nucleotide polymorphic variant of the RET proto-oncogene is underrepresented in sporadic Hirschsprung disease.

Griseri P, Sancandi M, Patrone G, Bocciardi R, Hofstra R, Ravazzolo R, Devoto M, Romeo G, Ceccherini I. Griseri P, et al. Among authors: romeo g. Eur J Hum Genet. 2000 Sep;8(9):721-4. doi: 10.1038/sj.ejhg.5200521. Eur J Hum Genet. 2000. PMID: 10980580

9

Exon structure and flanking intronic sequences of the human RET proto-oncogene.

Ceccherini I, Bocciardi R, Luo Y, Pasini B, Hofstra R, Takahashi M, Romeo G. Ceccherini I, et al. Among authors: romeo g. Biochem Biophys Res Commun. 1993 Nov 15;196(3):1288-95. doi: 10.1006/bbrc.1993.2392. Biochem Biophys Res Commun. 1993. PMID: 7902707

10

A rare haplotype of the RET proto-oncogene is a risk-modifying allele in hirschsprung disease.

Griseri P, Pesce B, Patrone G, Osinga J, Puppo F, Sancandi M, Hofstra R, Romeo G, Ravazzolo R, Devoto M, Ceccherini I. Griseri P, et al. Among authors: romeo g. Am J Hum Genet. 2002 Oct;71(4):969-74. doi: 10.1086/342774. Epub 2002 Sep 4. Am J Hum Genet. 2002. PMID: 12214285 Free PMC article.

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