BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

164 related articles for article (PubMed ID: 8933345)

  • 1. Currarino triad with a terminal deletion 7q35-->qter.
    Masuno M; Imaizumi K; Aida N; Tanaka Y; Sekido K; Ohhama Y; Nishi T; Kuroki Y
    J Med Genet; 1996 Oct; 33(10):877-8. PubMed ID: 8933345
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. A gene for autosomal dominant sacral agenesis maps to the holoprosencephaly region at 7q36.
    Lynch SA; Bond PM; Copp AJ; Kirwan WO; Nour S; Balling R; Mariman E; Burn J; Strachan T
    Nat Genet; 1995 Sep; 11(1):93-5. PubMed ID: 7550324
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Microcephaly, sensorineural deafness and Currarino triad with duplication-deletion of distal 7q.
    Pavone P; Ruggieri M; Lombardo I; Sudi J; Biancheri R; Castellano-Chiodo D; Rossi A; Incorpora G; Nowak NJ; Christian SL; Pavone L; Dobyns WB
    Eur J Pediatr; 2010 Apr; 169(4):475-81. PubMed ID: 19838731
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. The Currarino triad: complex of anorectal malformation, sacral bony abnormality, and presacral mass.
    Kirks DR; Merten DF; Filston HC; Oakes WJ
    Pediatr Radiol; 1984; 14(4):220-5. PubMed ID: 6728549
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Complete familial Currarino triad. Report of three cases in one family.
    Kurosaki M; Kamitani H; Anno Y; Watanabe T; Hori T; Yamasaki T
    J Neurosurg; 2001 Jan; 94(1 Suppl):158-61. PubMed ID: 11147855
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Complete familial Currarino triad in association with Hirschsprung's disease: magnetic resonance imaging features and the spectrum of anorectal malformations.
    Kilickesmez O; Gol IH; Uzun M; Oruk C
    Acta Radiol; 2006 May; 47(4):422-6. PubMed ID: 16739705
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. [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]  

  • 12. 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]  

  • 13. [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]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. 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]  

  • 18. Minimal clinical expression of the holoprosencephaly spectrum and of Currarino syndrome due to different cytogenetic rearrangements deleting the Sonic Hedgehog gene and the HLXB9 gene at 7q36.3.
    Horn D; Tönnies H; Neitzel H; Wahl D; Hinkel GK; von Moers A; Bartsch O
    Am J Med Genet A; 2004 Jul; 128A(1):85-92. PubMed ID: 15211664
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [The Currarino triad. An autosomal-dominant inherited complex of anorectal malformation, sacrococcygeal defect and presacral tumor. Observation of 9 further cases].
    Holthusen W; Birtel T; Brinkmann B; Gunkel J; Janneck C; Richter E
    Rofo; 1985 Jul; 143(1):83-9. PubMed ID: 2992020
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Currarino triad : a case report].
    Miyake S; Kamikawa S; Kojima N; Yamamoto K; Kobayashi N; Yamazato M; Higashimoto Y; Tsugawa C; Kanegawa K; Tamaki N
    No Shinkei Geka; 1996 Feb; 24(2):189-93. PubMed ID: 8849481
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.