BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

135 related articles for article (PubMed ID: 16254195)

  • 21. 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]  

  • 22. 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]  

  • 23. 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]  

  • 24. Novel MNX1 mutations and genotype-phenotype analysis of patients with Currarino syndrome.
    Han L; Zhang Z; Wang H; Song H; Gao Q; Yan Y; Tao R; Xiao P; Li L; Jiang Q; Li Q
    Orphanet J Rare Dis; 2020 Jun; 15(1):155. PubMed ID: 32571425
    [TBL] [Abstract][Full Text] [Related]  

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

  • 26. 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]  

  • 27. 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]  

  • 28. 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]  

  • 29. 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]  

  • 30. Currarino syndrome: a comprehensive genetic review of a rare congenital disorder.
    Dworschak GC; Reutter HM; Ludwig M
    Orphanet J Rare Dis; 2021 Apr; 16(1):167. PubMed ID: 33836786
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Whole exome sequencing of sporadic patients with Currarino Syndrome: A report of three trios.
    Holm I; Spildrejorde M; Stadheim B; Eiklid KL; Samarakoon PS
    Gene; 2017 Aug; 624():50-55. PubMed ID: 28456592
    [TBL] [Abstract][Full Text] [Related]  

  • 32. [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]  

  • 33. Currarino syndrome with pelvic neuroendocrine tumor diagnosed by post-mortem genetic analysis of tissue specimens.
    Ciotti P; Mandich P; Bellone E; Ceppa P; Bovio M; Ameri P; Torre G; Fiocca R; Murialdo G
    Am J Med Genet A; 2011 Nov; 155A(11):2750-3. PubMed ID: 21915987
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Comprehensive review of the duplication 3q syndrome and report of a patient with Currarino syndrome and de novo duplication 3q26.32-q27.2.
    Dworschak GC; Crétolle C; Hilger A; Engels H; Korsch E; Reutter H; Ludwig M
    Clin Genet; 2017 May; 91(5):661-671. PubMed ID: 27549440
    [TBL] [Abstract][Full Text] [Related]  

  • 35. 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]  

  • 36. 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]  

  • 37. 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]  

  • 38. 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]  

  • 39. Autosomal dominant sacral agenesis: Currarino syndrome.
    Lynch SA; Wang Y; Strachan T; Burn J; Lindsay S
    J Med Genet; 2000 Aug; 37(8):561-6. PubMed ID: 10922380
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Currarino syndrome: repair of the dysraphic anomalies and resection of the presacral mass in a combined neurosurgical and general surgical approach.
    Cearns MD; Hettige S; De Coppi P; Thompson DNP
    J Neurosurg Pediatr; 2018 Nov; 22(5):584-590. PubMed ID: 30095346
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.