246 related articles for article (PubMed ID: 21763840)
1. 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]
2. Novel MNX1 mutations and clinical analysis of familial and sporadic Currarino cases.
Merello E; De Marco P; Ravegnani M; Riccipetitoni G; Cama A; Capra V
Eur J Med Genet; 2013 Dec; 56(12):648-54. PubMed ID: 24095820
[TBL] [Abstract][Full Text] [Related]
3. Presacral teratoma in a Curarrino syndrome woman with an unreported insertion in MNX1 gene.
Lin YH; Huang RL; Lai HC
Taiwan J Obstet Gynecol; 2011 Dec; 50(4):512-4. PubMed ID: 22212327
[TBL] [Abstract][Full Text] [Related]
4. 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; 507(1):50-3. PubMed ID: 22820079
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Spectrum of MNX1 Pathogenic Variants and Associated Clinical Features in Korean Patients with Currarino Syndrome.
Lee S; Kim EJ; Cho SI; Park H; Seo SH; Seong MW; Park SS; Jung SE; Lee SC; Park KW; Kim HY
Ann Lab Med; 2018 May; 38(3):242-248. PubMed ID: 29401559
[TBL] [Abstract][Full Text] [Related]
7. Currarino syndrome: variable imaging features in three siblings with HLXB9 gene mutation.
Kim AY; Yoo SY; Kim JH; Eo H; Jeon TY
Clin Imaging; 2013; 37(2):398-402. PubMed ID: 23466002
[TBL] [Abstract][Full Text] [Related]
8. Presacral neuroendocrine tumors associated with the Currarino syndrome.
Scott AT; Tessmann JB; Braun T; Brown B; Breheny PJ; Darbro BW; Bellizzi AM; Dillon JS; O'Dorisio TM; Alderson A; Bennett B; Bernat JA; Metz DC; Howe JR
Am J Med Genet A; 2021 May; 185(5):1582-1588. PubMed ID: 33650152
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. [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]
11. Currarino syndrome: does the presence of a genetic anomaly correlate with a more severe phenotype? A multicentre study.
Costanzo S; Spaccini L; Pio L; Mattioli G; Virgone C; Dall'Igna P; Iacobelli B; Inserra A; Brisighelli G; Fagnani AM; Leva E; Giannotti G; Cheli M; Frumento P; Riccipetitoni G
J Pediatr Surg; 2017 Oct; 52(10):1591-1596. PubMed ID: 28689883
[TBL] [Abstract][Full Text] [Related]
12. [Radiological findings in Currarino syndrome].
Pérez Vega-Leal C; Sainz Gómez C; Ubis Rodríguez E; Garrido-Domínguez E; Díez Fernández A; Rubio Viguera V
Radiologia; 2013; 55(3):233-8. PubMed ID: 22237391
[TBL] [Abstract][Full Text] [Related]
13. Currarino syndrome at Rikshospitalet 1961-2012.
Monclair T; Lundar T; Smevik B; Holm I; Ørstavik KH
Tidsskr Nor Laegeforen; 2013 Nov; 133(22):2364-8. PubMed ID: 24287836
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. HLXB9 homeobox gene and caudal regression syndrome.
Merello E; De Marco P; Mascelli S; Raso A; Calevo MG; Torre M; Cama A; Lerone M; Martucciello G; Capra V
Birth Defects Res A Clin Mol Teratol; 2006 Mar; 76(3):205-9. PubMed ID: 16498628
[TBL] [Abstract][Full Text] [Related]
17. The first case of mosaic MNX1 mutation in an adult female with features of Currarino syndrome.
Romano F; De Marco P; Ognibene M; Di Duca M; Baldassari S; Pavanello M; Piatelli G; Zara F; Capra V
Birth Defects Res; 2021 Sep; 113(15):1161-1165. PubMed ID: 34156759
[TBL] [Abstract][Full Text] [Related]
18. Spectrum of HLXB9 gene mutations in Currarino syndrome and genotype-phenotype correlation.
Crétolle C; Pelet A; Sanlaville D; Zérah M; Amiel J; Jaubert F; Révillon Y; Baala L; Munnich A; Nihoul-Fékété C; Lyonnet S
Hum Mutat; 2008 Jul; 29(7):903-10. PubMed ID: 18449898
[TBL] [Abstract][Full Text] [Related]
19. MNX1 (HLXB9) mutations in Currarino patients.
Garcia-Barceló MM; Lui VC; So MT; Miao X; Leon TY; Yuan ZW; Ngan ES; Ehsan T; Chung PH; Khong PL; Wong KK; Tam PK
J Pediatr Surg; 2009 Oct; 44(10):1892-8. PubMed ID: 19853743
[TBL] [Abstract][Full Text] [Related]
20. Clinical features and HLXB9 gene mutation of a sporadic Chinese Currarino's syndrome case.
Liang Y; Wang J; Cai W
J Pediatr Surg; 2007 Jun; 42(6):E27-30. PubMed ID: 17560192
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
