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Low frequency of RET mutations in Hirschsprung disease in Sweden.
Svensson PJ, Molander ML, Eng C, Anvret M, Nordenskjöld A. Svensson PJ, et al. Clin Genet. 1998 Jul;54(1):39-44. doi: 10.1111/j.1399-0004.1998.tb03691.x. Clin Genet. 1998. PMID: 9727738
Laparoscopic-assisted pull-through for Hirschsprung's disease, a prospective repeated evaluation of functional outcome.
Granström AL, Husberg B, Nordenskjöld A, Svensson PJ, Wester T. Granström AL, et al. Among authors: svensson pj. J Pediatr Surg. 2013 Dec;48(12):2536-9. doi: 10.1016/j.jpedsurg.2013.07.017. J Pediatr Surg. 2013. PMID: 24314199 Clinical Trial.
Nerve growth factor receptor immunohistochemistry has a limited additional value to diagnose Hirschsprung's disease.
Granström AL, Orrego A, Svensson PJ, Almström M, Skikuniene J, Wester T. Granström AL, et al. Among authors: svensson pj. Pediatr Surg Int. 2011 Apr;27(4):431-5. doi: 10.1007/s00383-010-2728-9. Epub 2010 Sep 17. Pediatr Surg Int. 2011. PMID: 20848287
A heterozygous frameshift mutation in the endothelin-3 (EDN-3) gene in isolated Hirschsprung's disease.
Svensson PJ, Von Tell D, Molander ML, Anvret M, Nordenskjöld A. Svensson PJ, et al. Pediatr Res. 1999 May;45(5 Pt 1):714-7. doi: 10.1203/00006450-199905010-00018. Pediatr Res. 1999. PMID: 10231870
Mutations in the endothelin-receptor B gene in Hirschsprung disease in Sweden.
Svensson PJ, Tapper-Persson M, Anvret M, Molander ML, Eng C, Nordenskjöld A. Svensson PJ, et al. Clin Genet. 1999 Mar;55(3):215-7. doi: 10.1034/j.1399-0004.1999.550312.x. Clin Genet. 1999. PMID: 10334478 No abstract available.
Phenotypic variation in a family with mutations in two Hirschsprung-related genes (RET and endothelin receptor B).
Svensson PJ, Anvret M, Molander ML, Nordenskjöld A. Svensson PJ, et al. Hum Genet. 1998 Aug;103(2):145-8. doi: 10.1007/s004390050797. Hum Genet. 1998. PMID: 9760196
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. Zu S, et al. Among authors: svensson pj. J Pediatr Surg. 2011 Jul;46(7):1390-5. doi: 10.1016/j.jpedsurg.2011.02.039. J Pediatr Surg. 2011. PMID: 21763840
Mutation screening and array comparative genomic hybridization using a 180K oligonucleotide array in VACTERL association.
Winberg J, Gustavsson P, Papadogiannakis N, Sahlin E, Bradley F, Nordenskjöld E, Svensson PJ, Annerén G, Iwarsson E, Nordgren A, Nordenskjöld A. Winberg J, et al. Among authors: svensson pj. PLoS One. 2014 Jan 9;9(1):e85313. doi: 10.1371/journal.pone.0085313. eCollection 2014. PLoS One. 2014. PMID: 24416387 Free PMC article.
Supraumbilical incision with U-u umbilicoplasty for congenital duodenal atresia: the Stockholm experience.
Ghaffarpour N, Svensson PJ, Svenningsson A, Wester T, Mesas Burgos C. Ghaffarpour N, et al. Among authors: svensson pj. J Pediatr Surg. 2013 Sep;48(9):1981-5. doi: 10.1016/j.jpedsurg.2013.06.028. J Pediatr Surg. 2013. PMID: 24074679
Functional outcome and health-related quality of life in patients with sacrococcygeal teratoma - a Swedish multicenter study.
Hambraeus M, Al-Mashhadi A, Wester T, Svensson PJ, Stenström P, Lilja HE. Hambraeus M, et al. Among authors: svensson pj. J Pediatr Surg. 2019 Aug;54(8):1638-1643. doi: 10.1016/j.jpedsurg.2018.10.044. Epub 2018 Oct 22. J Pediatr Surg. 2019. PMID: 30420172
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