These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

208 related articles for article (PubMed ID: 10631160)

  • 1. Involvement of the HLXB9 homeobox gene in Currarino syndrome.
    Belloni E; Martucciello G; Verderio D; Ponti E; Seri M; Jasonni V; Torre M; Ferrari M; Tsui LC; Scherer SW
    Am J Hum Genet; 2000 Jan; 66(1):312-9. PubMed ID: 10631160
    [No Abstract]   [Full Text] [Related]  

  • 2. [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]  

  • 3. Preimplantation diagnosis for homeobox gene HLXB9 mutation causing Currarino syndrome.
    Verlinsky Y; Rechitsky S; Schoolcraft W; Kuliev A
    Am J Med Genet A; 2005 Apr; 134A(1):103-4. PubMed ID: 15776399
    [No Abstract]   [Full Text] [Related]  

  • 4. A previously unreported mutation in a Currarino syndrome kindred.
    Wang RY; Jones JR; Chen S; Rogers RC; Friez MJ; Schwartz CE; Graham JM
    Am J Med Genet A; 2006 Sep; 140(18):1923-30. PubMed ID: 16906559
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. A novel HLXB9 mutation in a Chinese family with Currarino syndrome.
    Wang Y; Wu Y
    Eur J Pediatr Surg; 2012 Jun; 22(3):243-5. PubMed ID: 21960426
    [No Abstract]   [Full Text] [Related]  

  • 8. 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. PubMed ID: 17612791
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. Currarino syndrome and spinal dysraphism.
    Kole MJ; Fridley JS; Jea A; Bollo RJ
    J Neurosurg Pediatr; 2014 Jun; 13(6):685-9. PubMed ID: 24745342
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Adult index patient with Currarino syndrome due to a novel HLXB9 mutation, c.336dupG (p.P113fsX224), presenting with Hirschsprung's disease, cephalgia, and lumbodynia.
    Volk A; Karbasiyan M; Semmler A; Todt U; Urbach H; Klockgether T; Linnebank M
    Birth Defects Res A Clin Mol Teratol; 2007 Mar; 79(3):249-51. PubMed ID: 17183586
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Population differences in the polyalanine domain and 6 new mutations in HLXB9 in patients with Currarino syndrome.
    Garcia-Barceló M; So MT; Lau DK; Leon TY; Yuan ZW; Cai WS; Lui VC; Fu M; Herbrick JA; Gutter E; Proud V; Li L; Pierre-Louis J; Aleck K; van Heurn E; Belloni E; Scherer SW; Tam PK
    Clin Chem; 2006 Jan; 52(1):46-52. PubMed ID: 16254195
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. [Currarino syndrome--a case report].
    Moshekov E; Ionkov A
    Khirurgiia (Sofiia); 2006; (3):59-60. PubMed ID: 18785437
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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. PubMed ID: 15359381
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. [Currarino triad: characteristic imaging appearances].
    Gabaudan C; Desmots F; Cerdan F; Soulier B; Richez P
    Presse Med; 2010 Oct; 39(10):1112-3. PubMed ID: 20462734
    [No 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]
    of 11.