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Items: 1 to 20 of 85

1.

Does Ser364Pro mutation of connexin 43 exist in Taiwanese patients with Ivemark syndrome?

Chen WC, Tsai FJ, Wu JY, Wu HC, Li CW.

Zhonghua Yi Xue Za Zhi (Taipei). 2000 Sep;63(9):691-5.

PMID:
11037645
2.

Mutation analysis of human LEFTY A and LEFTY B genes in children with Ivemark syndrome.

Chen WC, Tsai FJ, Wu JY, Shi YR, Wu HC.

Acta Paediatr Taiwan. 2000 Sep-Oct;41(5):259-62.

PMID:
11100524
3.

Ivemark syndrome in siblings.

Hurwitz RC, Caskey CT.

Clin Genet. 1982 Jul;22(1):7-11.

PMID:
7172476
4.

Failure to detect connexin43 mutations in 38 cases of sporadic and familial heterotaxy.

Gebbia M, Towbin JA, Casey B.

Circulation. 1996 Oct 15;94(8):1909-12.

5.

[Familial heterotaxy syndrome. Case report and review of the international literature].

Cesko I, Hajdú J, Marton T, Tarnai L, Zs Tóth E.

Orv Hetil. 1998 Nov 15;139(46):2775-8. Review. Hungarian.

PMID:
9849063
6.

Ivemark syndrome with asplenia in siblings.

Cesko I, Hajdú J, Tóth T, Marton T, Papp C, Papp Z.

J Pediatr. 1997 May;130(5):822-4.

PMID:
9152295
7.

Mutations of connexin43 in fetuses with congenital heart malformations.

Chen P, Xie LJ, Huang GY, Zhao XQ, Chang C.

Chin Med J (Engl). 2005 Jun 20;118(12):971-6.

PMID:
15978203
8.

Ivemark syndrome with agenesis of the corpus callosum: a case report with a review of the literature.

Noack F, Sayk F, Ressel A, Berg C, Gembruch U, Reusche E.

Prenat Diagn. 2002 Nov;22(11):1011-5. Review.

PMID:
12424766
9.

Functional characterization of connexin43 mutations found in patients with oculodentodigital dysplasia.

Shibayama J, Paznekas W, Seki A, Taffet S, Jabs EW, Delmar M, Musa H.

Circ Res. 2005 May 27;96(10):e83-91. Epub 2005 May 5.

10.

[Asplenia syndrome(Ivemark syndrome)].

Yamaguchi M, Oshima Y.

Ryoikibetsu Shokogun Shirizu. 2000;(32):305-7. Review. Japanese. No abstract available.

PMID:
11212725
11.

[An unusual form of Ivemark syndrome].

Szendröi M, Egerváry M.

Orv Hetil. 1982 Oct 31;123(44):2725-7. Hungarian. No abstract available.

PMID:
7145434
12.

[Simultaneous occurrence of Ivemark syndrome and diprosopus].

Jójárt G.

Orv Hetil. 1980 Dec 14;121(50):3095. Hungarian. No abstract available.

PMID:
7220027
13.
14.

Gouty arthritis in a patient with Ivemark syndrome.

Bhattacharjee M, Friedman AW, Thiagarajan P.

South Med J. 1996 Aug;89(8):834-5. No abstract available.

PMID:
8701391
15.

Spina bifida and so-called asplenia syndrome occurring separately in sibs.

Van Went JJ, Van Went GF, Delleman JW, Becker AG.

Teratology. 1977 Apr;15(2):195-8.

PMID:
325678
16.

Ivemark syndrome in association with congenital septum transversum defect and pancreatic divisum.

Sharma S, Gangopadhyay AN, Sharma SP.

Indian J Gastroenterol. 2006 Mar-Apr;25(2):94-6.

PMID:
16763342
17.

Familial occurrence of Ivemark syndrome with splenic hypoplasia and asplenia in sibs.

Simpson J, Zellweger H.

J Med Genet. 1973 Sep;10(3):303-4. No abstract available.

18.

[Syndrome of visceral symmetry. 12 children with the Ivemark syndrome].

Bucek J, Vítek B.

Cesk Pediatr. 1970 Feb;25(2):89-93. Czech. No abstract available.

PMID:
5437702
19.

["Ivemark syndrome": severe congenital cyanogenic heart disease, complex thoraco-abdominal heterotaxia and asplenia or polysplenia].

Neimann N, Pernot C, Gentin G, Vert P, Worms AM.

Pediatrie. 1966 Jul-Aug;21(5):511-32. French. No abstract available.

PMID:
5943512
20.

[The "Ivemark syndrome" severe cyanogenic congenital cardiopathy, complex thoraco-abdominal heterotaxia and asplenia or polysplenia].

Neimann N, Pernot C, Vert P, Worms AM.

Arch Mal Coeur Vaiss. 1966 Jun;59(6):876-900. French. No abstract available.

PMID:
4960659

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