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Results: 20

Related Articles by Review for PubMed (Select 8852660)

1.

Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprung disease.

Amiel J, Attié T, Jan D, Pelet A, Edery P, Bidaud C, Lacombe D, Tam P, Simeoni J, Flori E, Nihoul-Fékété C, Munnich A, Lyonnet S.

Hum Mol Genet. 1996 Mar;5(3):355-7.

2.

[Molecular genetics of Hirschsprung disease: a model of multigenic neurocristopathy].

Amiel J, Salomon R, Attié-Bitach T, Touraine R, Steffann J, Pelet A, Nihoul-Fékété C, Vekemans M, Munnich A, Lyonnet S.

J Soc Biol. 2000;194(3-4):125-8. Review. French.

PMID:
11324313
3.

[From monogenic to polygenic: model of Hirschsprung disease].

Salomon R, Amiel J, Attié T, Pelet A, Munnich A, Lyonnet S.

Pathol Biol (Paris). 1998 Nov;46(9):705-7. Review. French.

PMID:
9885824
4.

EDNRB/EDN3 and Hirschsprung disease type II.

McCallion AS, Chakravarti A.

Pigment Cell Res. 2001 Jun;14(3):161-9. Review.

PMID:
11434563
5.

[Molecular basis of Hirschsprung disease].

Inoue M, Okada A.

Nihon Rinsho. 1998 Jan;56(1):249-57. Review. Japanese.

PMID:
9465697
6.

[Genetics of Hirschsprung disease].

Attié T, Salomon R, Amiel J, Edery P, Pelet A, Nihoul-Fékété C, Munnich A, Lyonnet S.

C R Seances Soc Biol Fil. 1996;190(5-6):549-56. Review. French.

PMID:
9074720
7.

[Endothelin B receptor system and Hirschsprung disease].

Inoue M, Kusafuka T, Okada A.

Nihon Rinsho. 1998 Jul;56(7):1876-80. Review. Japanese.

PMID:
9702069
8.

Mutations of the endothelin-B receptor and endothelin-3 genes in Hirschsprung's disease.

Kusafuka T, Puri P.

Pediatr Surg Int. 1997;12(1):19-23. Review.

PMID:
9035203
9.

Hirschsprung disease, associated syndromes and genetics: a review.

Amiel J, Sproat-Emison E, Garcia-Barcelo M, Lantieri F, Burzynski G, Borrego S, Pelet A, Arnold S, Miao X, Griseri P, Brooks AS, Antinolo G, de Pontual L, Clement-Ziza M, Munnich A, Kashuk C, West K, Wong KK, Lyonnet S, Chakravarti A, Tam PK, Ceccherini I, Hofstra RM, Fernandez R; Hirschsprung Disease Consortium.

J Med Genet. 2008 Jan;45(1):1-14. Epub 2007 Oct 26. Review.

PMID:
17965226
10.

Hirschsprung, RET-SOX and beyond: the challenge of examining non-mendelian traits (Review).

Pusch CM, Sasiadek MM, Blin N.

Int J Mol Med. 2002 Oct;10(4):367-70. Review.

PMID:
12239580
11.

Mutations in Hirschsprung disease: when does a mutation contribute to the phenotype.

Hofstra RM, Osinga J, Buys CH.

Eur J Hum Genet. 1997 Jul-Aug;5(4):180-5. Review.

PMID:
9359036
12.

Genetics of Hirschsprung disease.

Parisi MA, Kapur RP.

Curr Opin Pediatr. 2000 Dec;12(6):610-7. Review.

PMID:
11106284
13.

Pathogenesis of Hirschsprung's disease.

Martucciello G, Ceccherini I, Lerone M, Jasonni V.

J Pediatr Surg. 2000 Jul;35(7):1017-25. Review.

PMID:
10917288
14.

Hirschsprung disease in an infant with a contiguous gene syndrome of chromosome 13.

Shanske A, Ferreira JC, Leonard JC, Fuller P, Marion RW.

Am J Med Genet. 2001 Aug 15;102(3):231-6. Review.

PMID:
11484199
15.

Hirschsprung's disease as a model of complex genetic etiology.

Borrego S, Ruiz-Ferrer M, Fernández RM, Antiñolo G.

Histol Histopathol. 2013 Sep;28(9):1117-36. Epub 2013 Apr 19. Review.

PMID:
23605783
16.

The developmental etiology and pathogenesis of Hirschsprung disease.

Butler Tjaden NE, Trainor PA.

Transl Res. 2013 Jul;162(1):1-15. doi: 10.1016/j.trsl.2013.03.001. Epub 2013 Mar 22. Review.

17.

Hirschsprung disease: a developmental disorder of the enteric nervous system.

McKeown SJ, Stamp L, Hao MM, Young HM.

Wiley Interdiscip Rev Dev Biol. 2013 Jan-Feb;2(1):113-29. doi: 10.1002/wdev.57. Epub 2012 Apr 24. Review.

PMID:
23799632
18.

Endothelin receptor-mediated signaling in hirschsprung disease.

Chakravarti A.

Hum Mol Genet. 1996 Mar;5(3):303-7. Review. No abstract available.

19.

Advances in Hirschsprung disease genetics and treatment strategies: an update for the primary care pediatrician.

Burkardt DD, Graham JM Jr, Short SS, Frykman PK.

Clin Pediatr (Phila). 2014 Jan;53(1):71-81. doi: 10.1177/0009922813500846. Epub 2013 Sep 3. Review.

PMID:
24002048
20.

[Rodent models with genetically altered endothelin receptor gene].

Emoto N.

Nihon Rinsho. 2004 Sep;62 Suppl 9:598-601. Review. Japanese. No abstract available.

PMID:
15506456
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