245 related articles for article (PubMed ID: 9368268)
1. The genetics of anorectal malformations: a complex matter.
Lerone M; Bolino A; Martucciello G
Semin Pediatr Surg; 1997 Nov; 6(4):170-9. PubMed ID: 9368268
[TBL] [Abstract][Full Text] [Related]
2. 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. PubMed ID: 8740138
[TBL] [Abstract][Full Text] [Related]
3. Spectrum of mutations and genotype-phenotype analysis in Currarino syndrome.
Köchling J; Karbasiyan M; Reis A
Eur J Hum Genet; 2001 Aug; 9(8):599-605. PubMed ID: 11528505
[TBL] [Abstract][Full Text] [Related]
4. The Currarino triad: the variable expression.
Emans PJ; Kootstra G; Marcelis CL; Beuls EA; van Heurn LW
J Pediatr Surg; 2005 Aug; 40(8):1238-42. PubMed ID: 16080925
[TBL] [Abstract][Full Text] [Related]
5. [Currarino syndrome].
Estévez M; Miner I; Benito MA; Calvo C; Corcuera P; Nogués A; Eizaguirre I
Cir Pediatr; 2008 Jan; 21(1):49-51. PubMed ID: 18444392
[TBL] [Abstract][Full Text] [Related]
6. [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. PubMed ID: 1763932
[TBL] [Abstract][Full Text] [Related]
7. The diagnostic value of MRI fistulogram and MRI distal colostogram in patients with anorectal malformations.
Kavalcova L; Skaba R; Kyncl M; Rouskova B; Prochazka A
J Pediatr Surg; 2013 Aug; 48(8):1806-9. PubMed ID: 23932626
[TBL] [Abstract][Full Text] [Related]
8. Anorectal anomalies associated with or as part of other anomalies.
Cuschieri A;
Am J Med Genet; 2002 Jun; 110(2):122-30. PubMed ID: 12116249
[TBL] [Abstract][Full Text] [Related]
9. [Neurologic changes or vertebral malformations in children with anorectal malformations].
Marco Macian A; Piqueras A; García-Sala Viguer C; Camps Vilata B; Sequi Canet JM
An Esp Pediatr; 1992 Aug; 37(2):130-4. PubMed ID: 1416538
[TBL] [Abstract][Full Text] [Related]
10. Complete Currarino triad in all affected members of the same family.
Mavridis G; Livaditi E; Soutis M; Keramidas DC
Eur J Pediatr Surg; 2005 Oct; 15(5):369-73. PubMed ID: 16254853
[TBL] [Abstract][Full Text] [Related]
11. [Urogenital abnormalities associated with anorectal malformations].
Lortat-Jacob S; Nihoul-Fekete C; Pellerin D
Acta Urol Belg; 1990; 58(1):163-8. PubMed ID: 2371937
[TBL] [Abstract][Full Text] [Related]
12. Mutation analysis of the motor neuron and pancreas homeobox 1 (MNX1, former HLXB9) gene in Swedish patients with Currarino syndrome.
Zu S; Winberg J; Arnberg F; Palmer G; Svensson PJ; Wester T; Nordenskjöld A
J Pediatr Surg; 2011 Jul; 46(7):1390-5. PubMed ID: 21763840
[TBL] [Abstract][Full Text] [Related]
13. Urethral duplication in association with anorectal malformation.
Singal AK; Bhatnagar V; Agarwala S; Mitra DK
Eur J Pediatr Surg; 2006 Jun; 16(3):214-6. PubMed ID: 16909364
[TBL] [Abstract][Full Text] [Related]
14. The posterior urethra in anorectal malformations.
Mickelson JJ; MacNeily AE; Blair GK
J Pediatr Surg; 2007 Mar; 42(3):585-7. PubMed ID: 17336208
[TBL] [Abstract][Full Text] [Related]
15. A 5.8 kb deletion removing the entire MNX1 gene in a Norwegian family with Currarino syndrome.
Holm I; Monclair T; Lundar T; Stadheim B; Prescott TE; Eiklid KL
Gene; 2013 Apr; 518(2):457-60. PubMed ID: 23370340
[TBL] [Abstract][Full Text] [Related]
16. New clinical and therapeutic perspectives in Currarino syndrome (study of 29 cases).
Crétolle C; Zérah M; Jaubert F; Sarnacki S; Révillon Y; Lyonnet S; Nihoul-Fékété C
J Pediatr Surg; 2006 Jan; 41(1):126-31; discussion 126-31. PubMed ID: 16410121
[TBL] [Abstract][Full Text] [Related]
17. [Currarino syndrome: variability of imaging findings in 22 molecular-genetically identified (HLXB9 mutation) patients from five families].
Riebel T; Köchling J; Scheer I; Oellinger J; Reis A
Rofo; 2004 Apr; 176(4):564-9. PubMed ID: 15088182
[TBL] [Abstract][Full Text] [Related]
18. Congenital gastrointestinal anomalies in anorectal malformations: what relationship and management?
Casaccia G; Catalano OA; Bagolan P
Congenit Anom (Kyoto); 2009 Jun; 49(2):93-6. PubMed ID: 19489962
[TBL] [Abstract][Full Text] [Related]
19. Exclusion of the Sonic Hedgehog gene as responsible for Currarino syndrome and anorectal malformations with sacral hypodevelopment.
Seri M; Martucciello G; Paleari L; Bolino A; Priolo M; Salemi G; Forabosco P; Caroli F; Cusano R; Tocco T; Lerone M; Cama A; Torre M; Guys JM; Romeo G; Jasonni V
Hum Genet; 1999 Jan; 104(1):108-10. PubMed ID: 10071202
[TBL] [Abstract][Full Text] [Related]
20. 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. PubMed ID: 25691298
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]