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250 related items for PubMed ID: 22237391

  • 1. [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
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Currarino Syndrome and the Effect of a Large Anterior Sacral Meningocele on Distal Colostogram in an Anorectal Malformation.
    Lee JK, Towbin AJ.
    J Radiol Case Rep; 2016 Jun; 10(6):16-21. PubMed ID: 27761181
    [Abstract] [Full Text] [Related]

  • 4. 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 Jun; 37(2):398-402. PubMed ID: 23466002
    [Abstract] [Full Text] [Related]

  • 5. 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 01; 22(5):584-590. PubMed ID: 30095346
    [Abstract] [Full Text] [Related]

  • 6. 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 01; 46(7):1390-5. PubMed ID: 21763840
    [Abstract] [Full Text] [Related]

  • 7. Currarino syndrome with immature teratoma: A case report with review of literature.
    Behera G, Manekar A, Mahallik S, Sable M, Das K.
    J Cancer Res Ther; 2024 Apr 01; 20(3):1088-1091. PubMed ID: 39023623
    [Abstract] [Full Text] [Related]

  • 8. 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 01; 50(4):512-4. PubMed ID: 22212327
    [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 01; 185(5):1582-1588. PubMed ID: 33650152
    [Abstract] [Full Text] [Related]

  • 10. 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 01; 52(8):1260-1268. PubMed ID: 28065719
    [Abstract] [Full Text] [Related]

  • 11. 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 01; 56(12):648-54. PubMed ID: 24095820
    [Abstract] [Full Text] [Related]

  • 12. [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 01; 176(4):564-9. PubMed ID: 15088182
    [Abstract] [Full Text] [Related]

  • 13. Familial Currarino syndrome associated with Hirschsprung disease: two cases of a mother and daughter.
    Ohno K, Nakamura T, Azuma T, Nakaoka T, Takama Y, Hayashi H, Horiike M, Zenitani M, Higashio A.
    J Pediatr Surg; 2013 Jan 01; 48(1):233-8. PubMed ID: 23331821
    [Abstract] [Full Text] [Related]

  • 14. 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 01; 29(7):836-7. PubMed ID: 23823266
    [Abstract] [Full Text] [Related]

  • 15. 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 01; 89(1):109-14. PubMed ID: 25691298
    [Abstract] [Full Text] [Related]

  • 16. Currarino Syndrome in a Fetus, Infant, Child, and Adolescent: Spectrum of Clinical Presentations and Imaging Findings.
    Caro-Domínguez P, Bass J, Hurteau-Miller J.
    Can Assoc Radiol J; 2017 Feb 01; 68(1):90-95. PubMed ID: 27887934
    [Abstract] [Full Text] [Related]

  • 17. 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 01; 155A(11):2750-3. PubMed ID: 21915987
    [Abstract] [Full Text] [Related]

  • 18. 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 01; 94(1 Suppl):158-61. PubMed ID: 11147855
    [Abstract] [Full Text] [Related]

  • 19. [Currarino triad: different forms of presentation].
    Calleja Aguayo E, Estors Sastre B, Bragagnini Rodríguez P, Fustero de Miguel D, Martínez-Pardo NG, Eliás Pollina J.
    Cir Pediatr; 2012 Jul 01; 25(3):155-8. PubMed ID: 23480013
    [Abstract] [Full Text] [Related]

  • 20. Multiple neurosurgical treatments for different members of the same family with Currarino syndrome.
    Serratrice N, Fievet L, Albader F, Scavarda D, Dufour H, Fuentes S.
    Neurochirurgie; 2018 Jun 01; 64(3):211-215. PubMed ID: 29731315
    [Abstract] [Full Text] [Related]

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