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22. 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; 20(3):1088-1091. PubMed ID: 39023623 [TBL] [Abstract][Full Text] [Related]
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25. [Currarino syndrome. A rare cause of severe constipation. Case report and literature review]. Vargas-González R; Paniagua-Morgan F; Victoria G; De la Torre-Mondragón L; Manuel Aparicio J Rev Gastroenterol Mex; 2008; 73(2):80-4. PubMed ID: 19666251 [TBL] [Abstract][Full Text] [Related]
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27. Spectrum of mutations and genotype-phenotype analysis in Currarino syndrome. Köchling J; Karbasiyan M; Reis A Eur J Hum Genet; 2001 Aug; 9(8):599-605. PubMed ID: 11528505 [TBL] [Abstract][Full Text] [Related]
28. 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]
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30. Currarino Syndrome: A Rare Condition With Potential Connection to Neuroendocrine Tumors. Liu AJ; Halfdanarson TR; Sonbol MB Pancreas; 2020 Sep; 49(8):1104-1108. PubMed ID: 32833944 [TBL] [Abstract][Full Text] [Related]
31. 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; 64(3):211-215. PubMed ID: 29731315 [TBL] [Abstract][Full Text] [Related]
32. 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]
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34. [Currarino syndrome--a case report]. Moshekov E; Ionkov A Khirurgiia (Sofiia); 2006; (3):59-60. PubMed ID: 18785437 [TBL] [Abstract][Full Text] [Related]
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40. [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] [Previous] [Next] [New Search]