These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
180 related articles for article (PubMed ID: 22901924)
1. A case of Currarino's syndrome presenting as neonatal bowel obstruction. Sekaran P; Brindley N J Pediatr Surg; 2012 Aug; 47(8):1600-3. PubMed ID: 22901924 [TBL] [Abstract][Full Text] [Related]
2. Currarino's syndrome in twins presenting as neonatal intestinal obstruction--identical presentation in non-identical twins. Patel RV; De Coppi P; Kiely E; Pierro A BMJ Case Rep; 2014 Sep; 2014():. PubMed ID: 25199187 [TBL] [Abstract][Full Text] [Related]
3. Neonatal Currarino's syndrome presenting as intestinal obstruction. Patel RV; Shepherd G; Kumar H; Patwardhan N BMJ Case Rep; 2013 Oct; 2013():. PubMed ID: 24130205 [No Abstract] [Full Text] [Related]
4. 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]
5. 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]
6. 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; 37(2):398-402. PubMed ID: 23466002 [TBL] [Abstract][Full Text] [Related]
9. 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 [TBL] [Abstract][Full Text] [Related]
10. Currarino's triad diagnosed in an adult woman. Berghauser Pont LM; Dirven CM; Dammers R Eur Spine J; 2012 Jun; 21 Suppl 4(Suppl 4):S569-72. PubMed ID: 22526704 [TBL] [Abstract][Full Text] [Related]
11. 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; 50(4):512-4. PubMed ID: 22212327 [TBL] [Abstract][Full Text] [Related]
12. 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]
13. Presacral masses in children: presentation, aetiology and risk of malignancy. Bartels SA; van Koperen PJ; van der Steeg AF; Deurloo EE; Bemelman WA; Heij HA Colorectal Dis; 2011 Aug; 13(8):930-4. PubMed ID: 20478006 [TBL] [Abstract][Full Text] [Related]
14. 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; 22(5):584-590. PubMed ID: 30095346 [TBL] [Abstract][Full Text] [Related]
15. [Currarino's triad: anorectal malformation, sacral anomaly and presacral mass]. Arifi M; Kaddouri N; Abdelhak M; Benhmamouch MN; Barahioui M Gastroenterol Clin Biol; 2006 Jan; 30(1):139-41. PubMed ID: 16514396 [TBL] [Abstract][Full Text] [Related]
17. Clinical features and HLXB9 gene mutation of a sporadic Chinese Currarino's syndrome case. Liang Y; Wang J; Cai W J Pediatr Surg; 2007 Jun; 42(6):E27-30. PubMed ID: 17560192 [TBL] [Abstract][Full Text] [Related]
18. Rare malignant neuroendocrine transformation of a presacral teratoma in patient with Currarino syndrome. Pendlimari R; Leonard D; Dozois EJ Int J Colorectal Dis; 2010 Nov; 25(11):1383-4. PubMed ID: 20532537 [No Abstract] [Full Text] [Related]
19. 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]
20. 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; 56(12):648-54. PubMed ID: 24095820 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]