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Journal Abstract Search

166 related items for PubMed ID: 33650152

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

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

  • 3. 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 15; 518(2):457-60. PubMed ID: 23370340
    [Abstract] [Full Text] [Related]

  • 4. 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 15; 50(4):512-4. PubMed ID: 22212327
    [Abstract] [Full Text] [Related]

  • 5. 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 15; 624():50-55. PubMed ID: 28456592
    [Abstract] [Full Text] [Related]

  • 6. 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 15; 56(12):648-54. PubMed ID: 24095820
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  • 9. 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 15; 38(3):242-248. PubMed ID: 29401559
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  • 10. Carcinoid transformation of presacral dermoid cyst in patient with currarino syndrome: a case report.
    Colombo F, Janous P, Buxton N.
    Br J Neurosurg; 2019 Jun 15; 33(3):285-286. PubMed ID: 28612626
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  • 11. Malignant transformation of presacral mass in Currarino syndrome.
    Rod J, Cretolle C, Faivre L, Jacquot C, Yacoub O, Ravasse P, Cheynel N, Sarnacki S.
    Pediatr Blood Cancer; 2019 Jun 15; 66(6):e27659. PubMed ID: 30740898
    [No Abstract] [Full Text] [Related]

  • 12. 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 15; 89(1):109-14. PubMed ID: 25691298
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  • 13. Currarino Syndrome: A Rare Condition With Potential Connection to Neuroendocrine Tumors.
    Liu AJ, Halfdanarson TR, Sonbol MB.
    Pancreas; 2020 Sep 15; 49(8):1104-1108. PubMed ID: 32833944
    [Abstract] [Full Text] [Related]

  • 14. A novel HLXB9 mutation in a Chinese family with Currarino syndrome.
    Wang Y, Wu Y.
    Eur J Pediatr Surg; 2012 Jun 15; 22(3):243-5. PubMed ID: 21960426
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  • 16. Currarino syndrome: a comprehensive genetic review of a rare congenital disorder.
    Dworschak GC, Reutter HM, Ludwig M.
    Orphanet J Rare Dis; 2021 Apr 09; 16(1):167. PubMed ID: 33836786
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  • 17. 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
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  • 18. Anterior sacral meningocele in a patient with currarino syndrome as a cause of ileus.
    Aydoseli A, Akcakaya MO, Aras Y, Dolas I, Yanar H, Sencer A.
    Br J Neurosurg; 2013 Dec 01; 27(6):833-5. PubMed ID: 23590527
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  • 19. 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 Dec 01; 37(2):398-402. PubMed ID: 23466002
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  • 20. 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 22; 15(1):155. PubMed ID: 32571425
    [Abstract] [Full Text] [Related]

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