148 related articles for article (PubMed ID: 34156759)
21. 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]
22. [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]
23. [Currarino syndrome--a case report].
Moshekov E; Ionkov A
Khirurgiia (Sofiia); 2006; (3):59-60. PubMed ID: 18785437
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Malignant degeneration of presacral teratoma in the Currarino anomaly.
Urioste M; Garcia-Andrade Mdel C; Valle L; Robledo M; González-Palacios F; Méndez R; Ferreirós J; Nuño J; Benítez J
Am J Med Genet A; 2004 Jul; 128A(3):299-304. PubMed ID: 15216552
[TBL] [Abstract][Full Text] [Related]
26. [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]
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. 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; 33(3):285-286. PubMed ID: 28612626
[TBL] [Abstract][Full Text] [Related]
29. 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]
30. Currarino triad: anorectal malformation, sacral bony abnormality, and presacral mass--a review of 11 cases.
Lee SC; Chun YS; Jung SE; Park KW; Kim WK
J Pediatr Surg; 1997 Jan; 32(1):58-61. PubMed ID: 9021570
[TBL] [Abstract][Full Text] [Related]
31. 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; 48(1):233-8. PubMed ID: 23331821
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. A previously unreported mutation in a Currarino syndrome kindred.
Wang RY; Jones JR; Chen S; Rogers RC; Friez MJ; Schwartz CE; Graham JM
Am J Med Genet A; 2006 Sep; 140(18):1923-30. PubMed ID: 16906559
[TBL] [Abstract][Full Text] [Related]
34. 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
[TBL] [Abstract][Full Text] [Related]
35. 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; 68(1):90-95. PubMed ID: 27887934
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. A novel HLXB9 mutation in a Chinese family with Currarino syndrome.
Wang Y; Wu Y
Eur J Pediatr Surg; 2012 Jun; 22(3):243-5. PubMed ID: 21960426
[No Abstract] [Full Text] [Related]
38. 18F-FDG PET/CT of Malignant Presacral Masses in Currarino Syndrome.
Nguyen BD
Clin Nucl Med; 2022 Feb; 47(2):e158-e160. PubMed ID: 35006115
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. 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; 27(6):833-5. PubMed ID: 23590527
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
