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 *

200 related articles for article (PubMed ID: 2604421)

  • 21. 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]  

  • 22. 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]  

  • 23. 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]  

  • 24. 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]  

  • 25. Currarino triad: surgical management and follow-up results of four [correction of three] cases.
    Isik N; Elmaci I; Gokben B; Balak N; Tosyali N
    Pediatr Neurosurg; 2010 Aug; 46(2):110-9. PubMed ID: 20664237
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Urodynamic evaluation of children with the caudal regression syndrome (caudal dysplasia sequence).
    Boemers TM; van Gool JD; de Jong TP; Bax KM
    J Urol; 1994 Apr; 151(4):1038-40. PubMed ID: 8126785
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. [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]  

  • 29. 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]  

  • 30. 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]  

  • 31. 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]  

  • 32. A locus for sacral/anorectal malformations maps to 6q25.3 in a 0.3 Mb interval region.
    Titomanlio L; Giurgea I; Baumann C; Elmaleh M; Sachs P; Chalard F; Aboura A; Verloes A
    Eur J Hum Genet; 2006 Aug; 14(8):971-4. PubMed ID: 16724010
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. A case of Currarino triad with familial sacral bony deformities.
    Iinuma Y; Iwafuchi M; Uchiyama M; Yagi M; Kondoh K; Ohtani S; Kanada S; Mishina T; Saitoh H; Suzuki N
    Pediatr Surg Int; 2000; 16(1-2):134-5. PubMed ID: 10663864
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Presentation of incomplete Currarino triad in a 12-day-old patient with vomiting: a case report.
    Kasem AJ; Pottker T
    Pediatr Emerg Care; 2013 Jul; 29(7):836-7. PubMed ID: 23823266
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Anorectal malformation: familial aspects and associated anomalies.
    Boocock GR; Donnai D
    Arch Dis Child; 1987 Jun; 62(6):576-9. PubMed ID: 3619473
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Currarino triad (anorectal malformation, sacral bony abnormality and presacral mass) with partial trisomy of chromosomes 13q and 20p.
    Nagai T; Katoh R; Hasegawa T; Ohashi H; Fukushima Y
    Clin Genet; 1994 May; 45(5):272-3. PubMed ID: 8076416
    [No Abstract]   [Full Text] [Related]  

  • 38. Pierre Robin syndrome with caudal regression syndrome-a rare combination of congenital syndromes.
    Ilyas M; Bashir I; Ellahi I; Shaheen F; Choh N
    Childs Nerv Syst; 2018 Jun; 34(6):1105-1106. PubMed ID: 29651537
    [No Abstract]   [Full Text] [Related]  

  • 39. 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]  

  • 40. Sharing of the same embryogenic pathway in anorectal malformations and anterior sacral myelomeningocele formation.
    Liu Y; Sugiyama F; Yagami K; Ohkawa H
    Pediatr Surg Int; 2003 May; 19(3):152-6. PubMed ID: 12682745
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.