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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1987 1
1992 1
1993 4
1994 10
1995 16
1996 13
1997 12
1998 14
1999 10
2000 9
2001 9
2002 8
2003 11
2004 2
2005 3
2006 1
2018 1
2020 3
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Similar Articles for PMID: 9565426

128 results
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Point mutation in exon 12 of the receptor tyrosine kinase proto-oncogene RET in Ondine-Hirschsprung syndrome.
Sakai T, Wakizaka A, Matsuda H, Nirasawa Y, Itoh Y. Sakai T, et al. Pediatrics. 1998 May;101(5):924-6. doi: 10.1542/peds.101.5.924. Pediatrics. 1998. PMID: 9565426
Congenital central hypoventilation syndrome associated with Hirschsprung's disease: mutation analysis of the RET and endothelin-signaling pathways.
Sakai T, Wakizaka A, Nirasawa Y. Sakai T, et al. Eur J Pediatr Surg. 2001 Oct;11(5):335-7. doi: 10.1055/s-2001-18552. Eur J Pediatr Surg. 2001. PMID: 11719874
Mutational analysis of multiple endocrine neoplasia type 2A associated with Hirschsprung's disease.
Borst MJ, VanCamp JM, Peacock ML, Decker RA. Borst MJ, et al. Surgery. 1995 Apr;117(4):386-91. doi: 10.1016/s0039-6060(05)80057-1. Surgery. 1995. PMID: 7716719
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
Point nucleotidic changes in both the RET proto-oncogene and the endothelin-B receptor gene in a Hirschsprung disease patient associated with Down syndrome.
Sakai T, Wakizaka A, Nirasawa Y, Ito Y. Sakai T, et al. Tohoku J Exp Med. 1999 Jan;187(1):43-7. doi: 10.1620/tjem.187.43. Tohoku J Exp Med. 1999. PMID: 10458491 Free article.
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. Biochem Biophys Res Commun. 1993 Nov 15;196(3):1288-95. doi: 10.1006/bbrc.1993.2392. Biochem Biophys Res Commun. 1993. PMID: 7902707
Familial form of hirschsprung disease: nucleotide sequence studies reveal point mutations in the RET proto-oncogene in two of six families but not in other candidate genes.
Munnes M, Fanaei S, Schmitz B, Muiznieks I, Holschneider AM, Doerfler W. Munnes M, et al. Am J Med Genet. 2000 Sep 4;94(1):19-27. doi: 10.1002/1096-8628(20000904)94:1<19::aid-ajmg5>3.0.co;2-k. Am J Med Genet. 2000. PMID: 10982477
Mutations of the RET proto-oncogene in Hirschsprung's disease.
Edery P, Lyonnet S, Mulligan LM, Pelet A, Dow E, Abel L, Holder S, Nihoul-Fékété C, Ponder BA, Munnich A. Edery P, et al. Nature. 1994 Jan 27;367(6461):378-80. doi: 10.1038/367378a0. Nature. 1994. PMID: 8114939
[Mutations of RET proto-oncogene in Hirschsprung disease].
Lyonnet S, Edery P, Mulligan LM, Pelet A, Dow E, Abel L, Holder S, Nihoul-Fékéte C, Ponder BA, Munnich A. Lyonnet S, et al. C R Acad Sci III. 1994 Apr;317(4):358-62. C R Acad Sci III. 1994. PMID: 8000915 French.
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