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Items: 1 to 20 of 26

1.

Clinical and genetic analysis of HLXB9 gene in Korean patients with Currarino syndrome.

Kim IS, Oh SY, Choi SJ, Kim JH, Park KH, Park HK, Kim JW, Ki CS.

J Hum Genet. 2007;52(8):698-701. Epub 2007 Jul 6.

PMID:
17612791
2.

Currarino syndrome: proposal of a diagnostic and therapeutic protocol.

Martucciello G, Torre M, Belloni E, Lerone M, Pini Prato A, Cama A, Jasonni V.

J Pediatr Surg. 2004 Sep;39(9):1305-11. Review.

PMID:
15359381
3.

The Currarino syndrome--hereditary transmitted syndrome of anorectal, sacral and presacral anomalies. Case report and review of the literature.

Köchling J, Pistor G, Märzhäuser Brands S, Nasir R, Lanksch WR.

Eur J Pediatr Surg. 1996 Apr;6(2):114-9. Review.

PMID:
8740138
4.

The genetics of anorectal malformations: a complex matter.

Lerone M, Bolino A, Martucciello G.

Semin Pediatr Surg. 1997 Nov;6(4):170-9. Review.

PMID:
9368268
5.

Comprehensive review of the duplication 3q syndrome and report of a patient with Currarino syndrome and de novo duplication 3q26.32-q27.2.

Dworschak GC, Crétolle C, Hilger A, Engels H, Korsch E, Reutter H, Ludwig M.

Clin Genet. 2017 May;91(5):661-671. doi: 10.1111/cge.12848. Epub 2016 Oct 10. Review.

PMID:
27549440
6.

Autosomal dominant sacral agenesis: Currarino syndrome.

Lynch SA, Wang Y, Strachan T, Burn J, Lindsay S.

J Med Genet. 2000 Aug;37(8):561-6. Review.

7.

[Currarino syndrome: an association not to be overlooked].

de Lagausie P, Munck A, Hertz Pannier L, Aigrain Y, Dupont A, Boureau M.

Arch Fr Pediatr. 1991 Nov;48(9):631-4. Review. French.

PMID:
1763932
8.

Phenotype analysis impacts testing strategy in patients with Currarino syndrome.

Cuturilo G, Hodge JC, Runke CK, Thorland EC, Al-Owain MA, Ellison JW, Babovic-Vuksanovic D.

Clin Genet. 2016 Jan;89(1):109-14. doi: 10.1111/cge.12572. Epub 2015 Mar 15. Review.

PMID:
25691298
9.

An unusual case of the complete Currarino triad: case report, discussion of the literature and the embryogenic implications.

Gegg CA, Vollmer DG, Tullous MW, Kagan-Hallet KS.

Neurosurgery. 1999 Mar;44(3):658-62. Review.

PMID:
10069605
10.

Currarino triad associated with malrotation of the colon.

Daoud FS, Aburub MA, Hadidy AM.

Saudi Med J. 2007 Feb;28(2):279-82. Review.

PMID:
17268712
11.

[Currarino syndrome. A rare cause of severe constipation. Case report and literature review].

Vargas-González R, Paniagua-Morgan F, Victoria G, De la Torre-Mondragón L, Manuel Aparicio J.

Rev Gastroenterol Mex. 2008;73(2):80-4. Review. Spanish.

PMID:
19666251
12.

Inheritance of familial congenital isolated anorectal malformations: case report and review.

Landau D, Mordechai J, Karplus M, Carmi R.

Am J Med Genet. 1997 Aug 22;71(3):280-2. Review.

PMID:
9268096
13.

Dubowitz syndrome: possible evidence for a clinical subtype.

Ilyina HG, Lurie IW.

Am J Med Genet. 1990 Apr;35(4):561-5. Review.

PMID:
2185633
14.

A case of Beare-Stevenson syndrome with a broad spectrum of features and a review of the FGFR2 Y375C mutation phenotype.

McGaughran J, Sinnott S, Susman R, Buckley MF, Elakis G, Cox T, Roscioli T.

Clin Dysmorphol. 2006 Apr;15(2):89-93. Review.

PMID:
16531735
15.

[Teratoma, presacral-sacral dysgenesis].

Kawame H.

Ryoikibetsu Shokogun Shirizu. 2001;(34 Pt 2):717-8. Review. Japanese. No abstract available.

PMID:
11528984
16.

Two coding single nucleotide polymorphisms in the SALL1 gene in Townes-Brocks syndrome: a case report and review of the literature.

Liang Y, Shen D, Cai W.

J Pediatr Surg. 2008 Feb;43(2):391-3. doi: 10.1016/j.jpedsurg.2007.09.079. Review.

PMID:
18280297
17.

Mortality and pathological findings in C (Opitz trigonocephaly) syndrome.

Opitz JM, Putnam AR, Comstock JM, Chin S, Byrne JL, Kennedy A, Frikke MJ, Bernard C, Albrecht S, Der Kaloustian V, Szakacs JG.

Fetal Pediatr Pathol. 2006 Jul-Aug;25(4):211-31. Review.

PMID:
17162528
18.

Anomalies of the forebrain with radial limb defects: Garcia-Lurie-Steinfeld syndrome?

McPherson E, Huff D, Dunn J, Muenke M.

Birth Defects Res A Clin Mol Teratol. 2004 Aug;70(8):537-44. Review.

PMID:
15329833
19.

[Sacrococcygeal malformations. Sixty seven cases].

Auvinet F, Chabrolle JP, Valayer J, Rossier A.

Ann Pediatr (Paris). 1978 Nov;25(9):479-84. Review. French. No abstract available.

PMID:
16114365
20.

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