Format
Items per page
Sort by

Send to:

Choose Destination

Links from PubMed

Items: 9

1.

Novel mutations in the MNX1 gene in two families with Currarino syndrome and variable phenotype.

Markljung E, Adamovic T, Cao J, Naji H, Kaiser S, Wester T, Nordenskjöld A.

Gene. 2012 Oct 1;507(1):50-3. doi: 10.1016/j.gene.2012.06.096. Epub 2012 Jul 20.

PMID:
22820079
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.

[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
4.

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
5.

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.

6.

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
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.

Review of genetic factors in intestinal malrotation.

Martin V, Shaw-Smith C.

Pediatr Surg Int. 2010 Aug;26(8):769-81. doi: 10.1007/s00383-010-2622-5. Epub 2010 Jun 13. Review.

9.

Milroy's primary congenital lymphedema in a male infant and review of the literature.

Kitsiou-Tzeli S, Vrettou C, Leze E, Makrythanasis P, Kanavakis E, Willems P.

In Vivo. 2010 May-Jun;24(3):309-14. Review.

PMID:
20555004
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk