228 related articles for article (PubMed ID: 29801510)
1. 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]
2. Currarino syndrome and spinal dysraphism.
Kole MJ; Fridley JS; Jea A; Bollo RJ
J Neurosurg Pediatr; 2014 Jun; 13(6):685-9. PubMed ID: 24745342
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. Currarino syndrome at Rikshospitalet 1961-2012.
Monclair T; Lundar T; Smevik B; Holm I; Ørstavik KH
Tidsskr Nor Laegeforen; 2013 Nov; 133(22):2364-8. PubMed ID: 24287836
[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]
7. 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; 38(3):242-248. PubMed ID: 29401559
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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; 29(7):836-7. PubMed ID: 23823266
[TBL] [Abstract][Full Text] [Related]
10. 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; 89(1):109-14. PubMed ID: 25691298
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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; 518(2):457-60. PubMed ID: 23370340
[TBL] [Abstract][Full Text] [Related]
13. 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; 624():50-55. PubMed ID: 28456592
[TBL] [Abstract][Full Text] [Related]
14. [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]
15. 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]
16. 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
[TBL] [Abstract][Full Text] [Related]
17. First case of Currarino syndrome and trimethylaminuria: two rare diseases for a complex clinical presentation.
Scimone C; Donato L; Rinaldi C; Sidoti A; D'Angelo R
J Dig Dis; 2016 Sep; 17(9):628-632. PubMed ID: 27335202
[No Abstract] [Full Text] [Related]
18. 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]
19. The Currarino triad: the variable expression.
Emans PJ; Kootstra G; Marcelis CL; Beuls EA; van Heurn LW
J Pediatr Surg; 2005 Aug; 40(8):1238-42. PubMed ID: 16080925
[TBL] [Abstract][Full Text] [Related]
20. [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]
[Next] [New Search]
