135 related articles for article (PubMed ID: 16254195)
41. A homeobox gene, HLXB9, is the major locus for dominantly inherited sacral agenesis.
Ross AJ; Ruiz-Perez V; Wang Y; Hagan DM; Scherer S; Lynch SA; Lindsay S; Custard E; Belloni E; Wilson DI; Wadey R; Goodman F; Orstavik KH; Monclair T; Robson S; Reardon W; Burn J; Scambler P; Strachan T
Nat Genet; 1998 Dec; 20(4):358-61. PubMed ID: 9843207
[TBL] [Abstract][Full Text] [Related]
42. Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.
Vieira V; David G; Roche O; de la Houssaye G; Boutboul S; Arbogast L; Kobetz A; Orssaud C; Camand O; Schorderet DF; Munier F; Rossi A; Delezoide AL; Marsac C; Ricquier D; Dufier JL; Menasche M; Abitbol M
Mol Vis; 2006 Dec; 12():1448-60. PubMed ID: 17167399
[TBL] [Abstract][Full Text] [Related]
43. 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]
44. Currarino syndrome and microcephaly due to a rare 7q36.2 microdeletion: a case report.
Cococcioni L; Paccagnini S; Pozzi E; Spaccini L; Cattaneo E; Redaelli S; Crosti F; Zuccotti GV
Ital J Pediatr; 2018 May; 44(1):59. PubMed ID: 29801510
[TBL] [Abstract][Full Text] [Related]
45. Multiple neurosurgical treatments for different members of the same family with Currarino syndrome.
Serratrice N; Fievet L; Albader F; Scavarda D; Dufour H; Fuentes S
Neurochirurgie; 2018 Jun; 64(3):211-215. PubMed ID: 29731315
[TBL] [Abstract][Full Text] [Related]
46. 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]
47. 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]
48. Unequal crossover recombination - population screening for PHOX2B gene polyalanine polymorphism using CE.
Hung CC; Su YN; Tsao PN; Chen PC; Lin SJ; Lin CH; Mu SC; Liu CA; Chang YC; Lin WL; Hsieh WS; Hsu SM
Electrophoresis; 2007 Mar; 28(6):894-9. PubMed ID: 17300129
[TBL] [Abstract][Full Text] [Related]
49. HLXB9 gene expression, and nuclear location during in vitro neuronal differentiation in the SK-N-BE neuroblastoma cell line.
Leotta CG; Federico C; Brundo MV; Tosi S; Saccone S
PLoS One; 2014; 9(8):e105481. PubMed ID: 25136833
[TBL] [Abstract][Full Text] [Related]
50. [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]
51. The Currarino triad: What pediatric surgeons need to know.
AbouZeid AA; Mohammad SA; Abolfotoh M; Radwan AB; Ismail MME; Hassan TA
J Pediatr Surg; 2017 Aug; 52(8):1260-1268. PubMed ID: 28065719
[TBL] [Abstract][Full Text] [Related]
52. [Image of the month. Abnormal gluteal crease revealing Currarino syndrome].
Jedidi Z; Moonen G
Rev Med Liege; 2012 Oct; 67(10):499-500. PubMed ID: 23167156
[No Abstract] [Full Text] [Related]
53. Treatment-resistant meningitis leading to the diagnosis of Currarino syndrome: a case report.
Kiefer AS; Gupta P; Kirmani S; Schwartz K; Henry N; Fischer PR
Pediatr Infect Dis J; 2009 Jun; 28(6):547-9. PubMed ID: 19483525
[TBL] [Abstract][Full Text] [Related]
54. [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]
55. [The Currarino syndrome: two case reports].
Di Meglio D; Capobianco A; Tramontano A; Gaglione G; Saggiomo G
Minerva Pediatr; 2005 Jun; 57(3):147-52. PubMed ID: 16170300
[TBL] [Abstract][Full Text] [Related]
56. Currarino triad--diagnostic dilemma and a combined surgical approach.
Samuel M; Hosie G; Holmes K
J Pediatr Surg; 2000 Dec; 35(12):1790-4. PubMed ID: 11101738
[TBL] [Abstract][Full Text] [Related]
57. 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]
58. Posterior sagittal approach for Currarino syndrome with anterior sacral meningocele: a case report.
Otagiri N; Matsumoto Y; Yoshida Y
J Pediatr Surg; 2000 Jul; 35(7):1112-4. PubMed ID: 10917308
[TBL] [Abstract][Full Text] [Related]
59. Polyalanine expansion in the ZIC3 gene leading to X-linked heterotaxy with VACTERL association: a new polyalanine disorder?
Wessels MW; Kuchinka B; Heydanus R; Smit BJ; Dooijes D; de Krijger RR; Lequin MH; de Jong EM; Husen M; Willems PJ; Casey B
J Med Genet; 2010 May; 47(5):351-5. PubMed ID: 20452998
[TBL] [Abstract][Full Text] [Related]
60. [Semiotics of the Currarino syndrome].
Pankevych TL; Lóniushkin OI; Sitkovskyĭ MB; Kaplan VM; Iurchenko MI; Cherniienko IuL
Klin Khir (1962); 1993; (12):20-3. PubMed ID: 8046863
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]