Кураринов синдром (Serbian Wikipedia)
Analysis of information sources in references of the Wikipedia article "Кураринов синдром" in Serbian language version.
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archive.org
- Currarino, G.; Coln, D.; Votteler, T. (1981). „Triad of anorectal, sacral, and presacral anomalies”. Am J Roentgenol. 137: 395—8..
- Belloni, E.; Martucciello, G.; Verderio, D.; Ponti, E.; Seri, M.; Jasonni, V.; Torre, M.; Ferrari, M.; Tsui, L.-C.; Scherer, S.W. (2000). „Involvement of the HLXB9 Homeobox Gene in Currarino Syndrome”. Am J Hum Genet. 66: 312—9. doi:10.1086/302723.
- Yates, V. D.; Wilroy RS; Whitington, I; Simmons JCH (1983). „Anterior sacral defects: an autosomal dominantly inherited condition”. J Pediatr. 102: 239—42..
- Garcia-Barceló, Mercè; So, Man-ting; Lau, Danny Ko-chun; Leon, Thomas Yuk-yu; Yuan, Zheng-wei; Cai, Wei-song; Lui, Vincent Chi-hang; Fu, Ming; Herbrick, Jo-Anne; Gutter, Emily; Proud, Virginia (2006-01-01). „Population Differences in the Polyalanine Domain and 6 New Mutations in HLXB9 in Patients with Currarino Syndrome”. Clinical Chemistry (на језику: енглески). 52 (1): 46—52. ISSN 0009-9147. PMID 16254195. doi:10.1373/clinchem.2005.056192
. - Kenefick, J. S. (1973). „Hereditary sacral agenesis associated with presacral tumours”. British Journal of Surgery. 60: 271—4..
- Ashcraft, K. W.; Holder, T. M. (1974). „Hereditary pre-sacral teratoma”. J Pediatr Surg. 9: 691—7..
- Kirks, D. R.; Merten DF; Filston, H. C.; Oakes, W. J. (1984). „The Currarino triad: complex of anorectal malformation, sacral bony defect, and presacral mass”. Pediatr Radiol. 14: 220—5..
- Ashcraft, K. W.; Holder, T. M. (1965). „Congenital anal stenosis with presacral teratoma: case reports”. Annals of Surgery. 162: 1091—5..
- Lynch, S. A.; Wang, Y; Strachan, T.; Burn, J; Lindsay, S. (2000). „Autosomal dominant sacral agenesis: Currarino syndrome”. J Med Genet. 37: 561—6.
- Ashcraft, Keith W.; Holder, Thomas M. (1974). „Hereditary presacral teratoma”. Journal of Pediatric Surgery. 9 (5): 691—697. PMID 4418917. doi:10.1016/0022-3468(74)90107-9.
- Belloni, E.; Martucciello, G.; Verderio, D.; Ponti, E.; Seri, M.; Jasonni, V.; Torre, M.; Ferrari, M.; Tsui, L.-C.; Scherer, S.W. (2000). „Involvement of the HLXB9 Homeobox Gene in Currarino Syndrome”. The American Journal of Human Genetics. 66 (1): 312—319. PMC 1288336 . PMID 10631160. doi:10.1086/302723..
- Gereige, R. S.; Frias, J. L. (2002). „Is it more than just constipation?”. Pediatrics. 109 (5): 961—5. PMID 11986463. doi:10.1542/peds.109.5.961.
- Garcia-Barceló, Mercè; So, Man-ting; Lau, Danny Ko-chun; Leon, Thomas Yuk-yu; Yuan, Zheng-wei; Cai, Wei-song; Lui, Vincent Chi-hang; Fu, Ming; Herbrick, Jo-Anne; Gutter, Emily; Proud, Virginia (2006-01-01). „Population Differences in the Polyalanine Domain and 6 New Mutations in HLXB9 in Patients with Currarino Syndrome”. Clinical Chemistry (на језику: енглески). 52 (1): 46—52. ISSN 0009-9147. PMID 16254195. doi:10.1373/clinchem.2005.056192 .
- Beuls, Emile A.M.; Vles, Johannes S.H.; Beets-Tan, Regina G.H.; Kootstra, Gauke; Marcelis, Carlo; Van Heurn, Ernest L.W.; Van Aalst, Jasper; Emans, Pieter J. (2006). „The Currarino Triad: Neurosurgical Considerations”. Neurosurgery. 58 (5): 924—929. PMID 16639328. S2CID 45316326. doi:10.1227/01.NEU.0000209945.87233.6A.
doi.org
- Belloni, E.; Martucciello, G.; Verderio, D.; Ponti, E.; Seri, M.; Jasonni, V.; Torre, M.; Ferrari, M.; Tsui, L.-C.; Scherer, S.W. (2000). „Involvement of the HLXB9 Homeobox Gene in Currarino Syndrome”. Am J Hum Genet. 66: 312—9. doi:10.1086/302723.
- AbouZeid, Amr Abdelhamid; Mohammad, Shaimaa Abdelsattar; Abolfotoh, Mohammad; Radwan, Ahmed Bassiouny; Ismail, Mohamed Mohamed ElSayed; Hassan, Tarek Ahmed (август 2017). „The Currarino triad: What pediatric surgeons need to know”. Journal of Pediatric Surgery (на језику: енглески). 52 (8): 1260—1268. PMID 28065719. doi:10.1016/j.jpedsurg.2016.12.010.
- Garcia-Barceló, Mercè; So, Man-ting; Lau, Danny Ko-chun; Leon, Thomas Yuk-yu; Yuan, Zheng-wei; Cai, Wei-song; Lui, Vincent Chi-hang; Fu, Ming; Herbrick, Jo-Anne; Gutter, Emily; Proud, Virginia (2006-01-01). „Population Differences in the Polyalanine Domain and 6 New Mutations in HLXB9 in Patients with Currarino Syndrome”. Clinical Chemistry (на језику: енглески). 52 (1): 46—52. ISSN 0009-9147. PMID 16254195. doi:10.1373/clinchem.2005.056192 .
- Dworschak, Gabriel C.; Reutter, Heiko M.; Ludwig, Michael (2021-04-09). „Currarino syndrome: a comprehensive genetic review of a rare congenital disorder”. Orphanet Journal of Rare Diseases. 16 (1): 167. ISSN 1750-1172. PMC 8034116 . PMID 33836786. doi:10.1186/s13023-021-01799-0 .
- Dirix, Marc; Van Becelaere, Tine; Berkenbosch, Lizanne; Van Baren, Robertine; Wijnen, Rene M.; Wijnen, Marc H.; Van Der Zee, David C.; Heij, Hugo A.; Derikx, Joep P.M.; Van Heurn, L.W. Ernest (2015). „Malignant transformation in sacrococcygeal teratoma and in presacral teratoma associated with Currarino syndrome: A comparative study”. J Pediatr Surg. 50 (3): 462—4. doi:10.1016/j.jpedsurg.2014.07.014.
- Crétolle, C.; Zérah, M.; Jaubert, F.; Sarnacki, S.; Révillon, Y.; Lyonnet, S.; Nihoul-Fékété, C. (2006). „New clinical and therapeutic perspectives in Currarino syndrome (Study of 29 cases)”. J Pediatr Surg. 41 (1): 126—31. PMID 16410121. doi:10.1016/j.jpedsurg.2005.10.053.
- Crétolle, C.; Pelet, A.; Sanlaville, D.; Zérah, M.; Amiel, J.; Jaubert, F.; Révillon, Y.; Baala, L.; Munnich, A.; Nihoul-Fékété, C.; Lyonnet, S. (2008). „Spectrum of HLXB9 gene mutations in Currarino syndrome and genotype-phenotype correlation”. Hum Mutat. 29 (7): 903—10. PMID 18449898. doi:10.1002/humu.20718.
- Gupta, Rahul; Sharma, Shyam Bihari; Mathur, Praveen; Goyal, Ram Babu (2014). „Variants of Currarino Syndrome: Embryological Association and Review of Pertinent Literature”. International Journal of Embryology. 2014: 1—5. doi:10.1155/2014/636375 ..
- Ashcraft, Keith W.; Holder, Thomas M. (1974). „Hereditary presacral teratoma”. Journal of Pediatric Surgery. 9 (5): 691—697. PMID 4418917. doi:10.1016/0022-3468(74)90107-9.
- Belloni, E.; Martucciello, G.; Verderio, D.; Ponti, E.; Seri, M.; Jasonni, V.; Torre, M.; Ferrari, M.; Tsui, L.-C.; Scherer, S.W. (2000). „Involvement of the HLXB9 Homeobox Gene in Currarino Syndrome”. The American Journal of Human Genetics. 66 (1): 312—319. PMC 1288336 . PMID 10631160. doi:10.1086/302723..
- Samuel, M.; Hosie, G.; Holmes, K. (2000). „Currarino triad—Diagnostic dilemma and a combined surgical approach”. J Pediatr Surg. 35 (12): 1790—4. PMID 11101738. doi:10.1053/jpsu.2000.19258. .
- Gereige, R. S.; Frias, J. L. (2002). „Is it more than just constipation?”. Pediatrics. 109 (5): 961—5. PMID 11986463. doi:10.1542/peds.109.5.961.
- „Currarino syndrome: does the presence of a genetic anomaly correlate with a more severe phenotype?”. J Pediatr Surg. 52: 1591—6. 2017. PMID 28689883. doi:10.1016/j.jpedsurg.2017.06.012.
- Garcia-Barceló, Mercè; So, Man-ting; Lau, Danny Ko-chun; Leon, Thomas Yuk-yu; Yuan, Zheng-wei; Cai, Wei-song; Lui, Vincent Chi-hang; Fu, Ming; Herbrick, Jo-Anne; Gutter, Emily; Proud, Virginia (2006-01-01). „Population Differences in the Polyalanine Domain and 6 New Mutations in HLXB9 in Patients with Currarino Syndrome”. Clinical Chemistry (на језику: енглески). 52 (1): 46—52. ISSN 0009-9147. PMID 16254195. doi:10.1373/clinchem.2005.056192 .
- Berghauser Pont LM, Dirven CM, Dammers R (2012). „Currarino's triad diagnosed in an adult woman”. Eur Spine J. 21 (Suppl 4): S569—72. PMC 3369045 . PMID 22526704. doi:10.1007/s00586-012-2311-2.
- Emoto S, Kaneko M, Murono K, Sasaki K, Otani K, Nishikawa T, Tanaka T, Hata K, Kawai K, Imai H, Saito N, Kobayashi H, Tanaka S, Ikemura M, Ushiku T, Nozawa H (2018). „Surgical management for a huge presacral teratoma and a meningocele in an adult with Currarino triad: a case report”. Surg Case Rep. 4 (1): 9. PMC 5775187 . PMID 29352751. doi:10.1186/s40792-018-0419-2 .
- Samuel, M.; Hosie, G.; Holmes, K. (децембар 2000). „Currarino triad--diagnostic dilemma and a combined surgical approach”. J Pediatr Surg. 35 (12): 1790—4. PMID 11101738. doi:10.1053/jpsu.2000.19258.
- Beuls, Emile A.M.; Vles, Johannes S.H.; Beets-Tan, Regina G.H.; Kootstra, Gauke; Marcelis, Carlo; Van Heurn, Ernest L.W.; Van Aalst, Jasper; Emans, Pieter J. (2006). „The Currarino Triad: Neurosurgical Considerations”. Neurosurgery. 58 (5): 924—929. PMID 16639328. S2CID 45316326. doi:10.1227/01.NEU.0000209945.87233.6A.
- Crétolle, Celia; Zérah, Michel; Jaubert, Francis; Sarnacki, Sabine; Révillon, Yann; Lyonnet, Stanislas; Nihoul-Fékété, Claire (2006). „New clinical and therapeutic perspectives in Currarino syndrome (Study of 29 cases)”. Journal of Pediatric Surgery. 41 (1): 126—131. PMID 16410121. doi:10.1016/j.jpedsurg.2005.10.053..
- Serratrice, N.; Fievet, L.; Albader, F.; Scavarda, D.; Dufour, H.; Fuentes, S. (2018). „Multiple neurosurgical treatments for different members of the same family with Currarino syndrome”. Neurochirurgie. 64 (3): 211—215. PMID 29731315. S2CID 19176774. doi:10.1016/j.neuchi.2018.01.009..
- Emoto, Shigenobu; Kaneko, Manabu; Murono, Koji; Sasaki, Kazuhito; Otani, Kensuke; Nishikawa, Takeshi; Tanaka, Toshiaki; Hata, Keisuke; Kawai, Kazushige; Imai, Hideaki; Saito, Nobuhito; Kobayashi, Hiroshi; Tanaka, Sakae; Ikemura, Masako; Ushiku, Tetsuo; Nozawa, Hiroaki (2018). „Surgical management for a huge presacral teratoma and a meningocele in an adult with Currarino triad: A case report”. Surgical Case Reports. 4 (1): 9. PMC 5775187 . PMID 29352751. doi:10.1186/s40792-018-0419-2 ..
- Kazemi, Noojan; Chakhalian, Daniel; Gunasekaran, Arunprasad; Gandhi, Gautam; Bradley, Lucas; Mizell, Jason (2017). „Multidisciplinary surgical treatment of presacral meningocele and teratoma in an adult with Currarino triad”. Surgical Neurology International. 8: 77. PMC 5445655 . PMID 28584680. doi:10.4103/sni.sni_439_16 ..
- Isik N, Elmaci I, Gokben B, Balak N, Tosyali N (2010). „Currarino triad: surgical management and follow-up results of four [correction of three] cases”. Pediatric Neurosurgery. 46 (2): 110—9. PMID 20664237. S2CID 30203031. doi:10.1159/000319007.
- Kansal R, Mahore A, Dange N, Kukreja S (2012). „Epidermoid cyst inside anterior sacral meningocele in an adult patient of Currarino syndrome manifesting with meningitis”. Turk Neurosurg. 22 (5): 659—61. PMID 23015348. doi:10.5137/1019-5149.JTN.3985-10.1 .
- Duru, Soner; Karabagli, Hakan; Turkoglu, Erhan; Erşahin, Yusuf (2014). „Currarino syndrome: Report of five consecutive patients”. Child's Nervous System. 30 (3): 547—552. PMID 24013264. S2CID 20214381. doi:10.1007/s00381-013-2274-6.
- Bergeron, Eric; Roux, Alain; Demers, Jacques; Vanier, Laurent E.; Moore, Lynne (2010). „A 40-Year-Old Woman with Cauda Equina Syndrome Caused by Rectothecal Fistula Arising from an Anterior Sacral Meningocele”. Neurosurgery. 67 (5): E1464—E1475. PMID 20871432. S2CID 31090668. doi:10.1227/NEU.0b013e3181f352ba.
nih.gov
ncbi.nlm.nih.gov
- AbouZeid, Amr Abdelhamid; Mohammad, Shaimaa Abdelsattar; Abolfotoh, Mohammad; Radwan, Ahmed Bassiouny; Ismail, Mohamed Mohamed ElSayed; Hassan, Tarek Ahmed (август 2017). „The Currarino triad: What pediatric surgeons need to know”. Journal of Pediatric Surgery (на језику: енглески). 52 (8): 1260—1268. PMID 28065719. doi:10.1016/j.jpedsurg.2016.12.010.
- Garcia-Barceló, Mercè; So, Man-ting; Lau, Danny Ko-chun; Leon, Thomas Yuk-yu; Yuan, Zheng-wei; Cai, Wei-song; Lui, Vincent Chi-hang; Fu, Ming; Herbrick, Jo-Anne; Gutter, Emily; Proud, Virginia (2006-01-01). „Population Differences in the Polyalanine Domain and 6 New Mutations in HLXB9 in Patients with Currarino Syndrome”. Clinical Chemistry (на језику: енглески). 52 (1): 46—52. ISSN 0009-9147. PMID 16254195. doi:10.1373/clinchem.2005.056192 .
- Dworschak, Gabriel C.; Reutter, Heiko M.; Ludwig, Michael (2021-04-09). „Currarino syndrome: a comprehensive genetic review of a rare congenital disorder”. Orphanet Journal of Rare Diseases. 16 (1): 167. ISSN 1750-1172. PMC 8034116 . PMID 33836786. doi:10.1186/s13023-021-01799-0 .
- Crétolle, C.; Zérah, M.; Jaubert, F.; Sarnacki, S.; Révillon, Y.; Lyonnet, S.; Nihoul-Fékété, C. (2006). „New clinical and therapeutic perspectives in Currarino syndrome (Study of 29 cases)”. J Pediatr Surg. 41 (1): 126—31. PMID 16410121. doi:10.1016/j.jpedsurg.2005.10.053.
- Crétolle, C.; Pelet, A.; Sanlaville, D.; Zérah, M.; Amiel, J.; Jaubert, F.; Révillon, Y.; Baala, L.; Munnich, A.; Nihoul-Fékété, C.; Lyonnet, S. (2008). „Spectrum of HLXB9 gene mutations in Currarino syndrome and genotype-phenotype correlation”. Hum Mutat. 29 (7): 903—10. PMID 18449898. doi:10.1002/humu.20718.
- Ashcraft, Keith W.; Holder, Thomas M. (1974). „Hereditary presacral teratoma”. Journal of Pediatric Surgery. 9 (5): 691—697. PMID 4418917. doi:10.1016/0022-3468(74)90107-9.
- Belloni, E.; Martucciello, G.; Verderio, D.; Ponti, E.; Seri, M.; Jasonni, V.; Torre, M.; Ferrari, M.; Tsui, L.-C.; Scherer, S.W. (2000). „Involvement of the HLXB9 Homeobox Gene in Currarino Syndrome”. The American Journal of Human Genetics. 66 (1): 312—319. PMC 1288336 . PMID 10631160. doi:10.1086/302723..
- Samuel, M.; Hosie, G.; Holmes, K. (2000). „Currarino triad—Diagnostic dilemma and a combined surgical approach”. J Pediatr Surg. 35 (12): 1790—4. PMID 11101738. doi:10.1053/jpsu.2000.19258. .
- Gereige, R. S.; Frias, J. L. (2002). „Is it more than just constipation?”. Pediatrics. 109 (5): 961—5. PMID 11986463. doi:10.1542/peds.109.5.961.
- „Currarino syndrome: does the presence of a genetic anomaly correlate with a more severe phenotype?”. J Pediatr Surg. 52: 1591—6. 2017. PMID 28689883. doi:10.1016/j.jpedsurg.2017.06.012.
- Garcia-Barceló, Mercè; So, Man-ting; Lau, Danny Ko-chun; Leon, Thomas Yuk-yu; Yuan, Zheng-wei; Cai, Wei-song; Lui, Vincent Chi-hang; Fu, Ming; Herbrick, Jo-Anne; Gutter, Emily; Proud, Virginia (2006-01-01). „Population Differences in the Polyalanine Domain and 6 New Mutations in HLXB9 in Patients with Currarino Syndrome”. Clinical Chemistry (на језику: енглески). 52 (1): 46—52. ISSN 0009-9147. PMID 16254195. doi:10.1373/clinchem.2005.056192 .
- Berghauser Pont LM, Dirven CM, Dammers R (2012). „Currarino's triad diagnosed in an adult woman”. Eur Spine J. 21 (Suppl 4): S569—72. PMC 3369045 . PMID 22526704. doi:10.1007/s00586-012-2311-2.
- Emoto S, Kaneko M, Murono K, Sasaki K, Otani K, Nishikawa T, Tanaka T, Hata K, Kawai K, Imai H, Saito N, Kobayashi H, Tanaka S, Ikemura M, Ushiku T, Nozawa H (2018). „Surgical management for a huge presacral teratoma and a meningocele in an adult with Currarino triad: a case report”. Surg Case Rep. 4 (1): 9. PMC 5775187 . PMID 29352751. doi:10.1186/s40792-018-0419-2 .
- Samuel, M.; Hosie, G.; Holmes, K. (децембар 2000). „Currarino triad--diagnostic dilemma and a combined surgical approach”. J Pediatr Surg. 35 (12): 1790—4. PMID 11101738. doi:10.1053/jpsu.2000.19258.
- Beuls, Emile A.M.; Vles, Johannes S.H.; Beets-Tan, Regina G.H.; Kootstra, Gauke; Marcelis, Carlo; Van Heurn, Ernest L.W.; Van Aalst, Jasper; Emans, Pieter J. (2006). „The Currarino Triad: Neurosurgical Considerations”. Neurosurgery. 58 (5): 924—929. PMID 16639328. S2CID 45316326. doi:10.1227/01.NEU.0000209945.87233.6A.
- Crétolle, Celia; Zérah, Michel; Jaubert, Francis; Sarnacki, Sabine; Révillon, Yann; Lyonnet, Stanislas; Nihoul-Fékété, Claire (2006). „New clinical and therapeutic perspectives in Currarino syndrome (Study of 29 cases)”. Journal of Pediatric Surgery. 41 (1): 126—131. PMID 16410121. doi:10.1016/j.jpedsurg.2005.10.053..
- Serratrice, N.; Fievet, L.; Albader, F.; Scavarda, D.; Dufour, H.; Fuentes, S. (2018). „Multiple neurosurgical treatments for different members of the same family with Currarino syndrome”. Neurochirurgie. 64 (3): 211—215. PMID 29731315. S2CID 19176774. doi:10.1016/j.neuchi.2018.01.009..
- Emoto, Shigenobu; Kaneko, Manabu; Murono, Koji; Sasaki, Kazuhito; Otani, Kensuke; Nishikawa, Takeshi; Tanaka, Toshiaki; Hata, Keisuke; Kawai, Kazushige; Imai, Hideaki; Saito, Nobuhito; Kobayashi, Hiroshi; Tanaka, Sakae; Ikemura, Masako; Ushiku, Tetsuo; Nozawa, Hiroaki (2018). „Surgical management for a huge presacral teratoma and a meningocele in an adult with Currarino triad: A case report”. Surgical Case Reports. 4 (1): 9. PMC 5775187 . PMID 29352751. doi:10.1186/s40792-018-0419-2 ..
- Kazemi, Noojan; Chakhalian, Daniel; Gunasekaran, Arunprasad; Gandhi, Gautam; Bradley, Lucas; Mizell, Jason (2017). „Multidisciplinary surgical treatment of presacral meningocele and teratoma in an adult with Currarino triad”. Surgical Neurology International. 8: 77. PMC 5445655 . PMID 28584680. doi:10.4103/sni.sni_439_16 ..
- Işik, N.; Balak, N.; Kircelli, A.; Göynümer, G.; Elmaci, I. (2008). „The shrinking of an anterior sacral meningocele in time following transdural ligation of its neck in a case of the Currarino triad”. Turkish Neurosurgery. 18 (3): 254—258. PMID 18814114.
- Isik N, Elmaci I, Gokben B, Balak N, Tosyali N (2010). „Currarino triad: surgical management and follow-up results of four [correction of three] cases”. Pediatric Neurosurgery. 46 (2): 110—9. PMID 20664237. S2CID 30203031. doi:10.1159/000319007.
- Kansal R, Mahore A, Dange N, Kukreja S (2012). „Epidermoid cyst inside anterior sacral meningocele in an adult patient of Currarino syndrome manifesting with meningitis”. Turk Neurosurg. 22 (5): 659—61. PMID 23015348. doi:10.5137/1019-5149.JTN.3985-10.1 .
- Duru, Soner; Karabagli, Hakan; Turkoglu, Erhan; Erşahin, Yusuf (2014). „Currarino syndrome: Report of five consecutive patients”. Child's Nervous System. 30 (3): 547—552. PMID 24013264. S2CID 20214381. doi:10.1007/s00381-013-2274-6.
- Bergeron, Eric; Roux, Alain; Demers, Jacques; Vanier, Laurent E.; Moore, Lynne (2010). „A 40-Year-Old Woman with Cauda Equina Syndrome Caused by Rectothecal Fistula Arising from an Anterior Sacral Meningocele”. Neurosurgery. 67 (5): E1464—E1475. PMID 20871432. S2CID 31090668. doi:10.1227/NEU.0b013e3181f352ba.
rarediseases.info.nih.gov
- „Currarino triad | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program”. rarediseases.info.nih.gov (на језику: енглески). Приступљено 2022-02-21.
semanticscholar.org
api.semanticscholar.org
- Beuls, Emile A.M.; Vles, Johannes S.H.; Beets-Tan, Regina G.H.; Kootstra, Gauke; Marcelis, Carlo; Van Heurn, Ernest L.W.; Van Aalst, Jasper; Emans, Pieter J. (2006). „The Currarino Triad: Neurosurgical Considerations”. Neurosurgery. 58 (5): 924—929. PMID 16639328. S2CID 45316326. doi:10.1227/01.NEU.0000209945.87233.6A.
- Serratrice, N.; Fievet, L.; Albader, F.; Scavarda, D.; Dufour, H.; Fuentes, S. (2018). „Multiple neurosurgical treatments for different members of the same family with Currarino syndrome”. Neurochirurgie. 64 (3): 211—215. PMID 29731315. S2CID 19176774. doi:10.1016/j.neuchi.2018.01.009..
- Isik N, Elmaci I, Gokben B, Balak N, Tosyali N (2010). „Currarino triad: surgical management and follow-up results of four [correction of three] cases”. Pediatric Neurosurgery. 46 (2): 110—9. PMID 20664237. S2CID 30203031. doi:10.1159/000319007.
- Duru, Soner; Karabagli, Hakan; Turkoglu, Erhan; Erşahin, Yusuf (2014). „Currarino syndrome: Report of five consecutive patients”. Child's Nervous System. 30 (3): 547—552. PMID 24013264. S2CID 20214381. doi:10.1007/s00381-013-2274-6.
- Bergeron, Eric; Roux, Alain; Demers, Jacques; Vanier, Laurent E.; Moore, Lynne (2010). „A 40-Year-Old Woman with Cauda Equina Syndrome Caused by Rectothecal Fistula Arising from an Anterior Sacral Meningocele”. Neurosurgery. 67 (5): E1464—E1475. PMID 20871432. S2CID 31090668. doi:10.1227/NEU.0b013e3181f352ba.
worldcat.org
- Garcia-Barceló, Mercè; So, Man-ting; Lau, Danny Ko-chun; Leon, Thomas Yuk-yu; Yuan, Zheng-wei; Cai, Wei-song; Lui, Vincent Chi-hang; Fu, Ming; Herbrick, Jo-Anne; Gutter, Emily; Proud, Virginia (2006-01-01). „Population Differences in the Polyalanine Domain and 6 New Mutations in HLXB9 in Patients with Currarino Syndrome”. Clinical Chemistry (на језику: енглески). 52 (1): 46—52. ISSN 0009-9147. PMID 16254195. doi:10.1373/clinchem.2005.056192 .
- Dworschak, Gabriel C.; Reutter, Heiko M.; Ludwig, Michael (2021-04-09). „Currarino syndrome: a comprehensive genetic review of a rare congenital disorder”. Orphanet Journal of Rare Diseases. 16 (1): 167. ISSN 1750-1172. PMC 8034116 . PMID 33836786. doi:10.1186/s13023-021-01799-0 .
- Garcia-Barceló, Mercè; So, Man-ting; Lau, Danny Ko-chun; Leon, Thomas Yuk-yu; Yuan, Zheng-wei; Cai, Wei-song; Lui, Vincent Chi-hang; Fu, Ming; Herbrick, Jo-Anne; Gutter, Emily; Proud, Virginia (2006-01-01). „Population Differences in the Polyalanine Domain and 6 New Mutations in HLXB9 in Patients with Currarino Syndrome”. Clinical Chemistry (на језику: енглески). 52 (1): 46—52. ISSN 0009-9147. PMID 16254195. doi:10.1373/clinchem.2005.056192 .