Svensson PJ - Search Results

1

PHOX2B genotype allows for prediction of tumor risk in congenital central hypoventilation syndrome.

Trochet D, O'Brien LM, Gozal D, Trang H, Nordenskjöld A, Laudier B, Svensson PJ, Uhrig S, Cole T, Niemann S, Munnich A, Gaultier C, Lyonnet S, Amiel J. Trochet D, et al. Among authors: svensson pj. Am J Hum Genet. 2005 Mar;76(3):421-6. doi: 10.1086/428366. Epub 2005 Jan 18. Am J Hum Genet. 2005. PMID: 15657873 Free PMC article.

2

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

3

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

4

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

5

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

6

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.

7

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.

8

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.

9

National centralization of Hirschsprung's disease in Sweden: a comparison of postoperative outcome.

Söderström L, Graneli C, Rossi D, Hagelsteen K, Gunnarsdottir A, Oddsberg J, Svensson PJ, Borg H, Bräutigam M, Gustafson E, Löf Granström A, Stenström P, Wester T. Söderström L, et al. Among authors: svensson pj. Pediatr Surg Int. 2024 Oct 5;40(1):265. doi: 10.1007/s00383-024-05842-6. Pediatr Surg Int. 2024. PMID: 39369074 Free PMC article.

10

Malignant transformation and tumour recurrence in sacrococcygeal teratoma: a global, retrospective cohort study.

van Heurn LJ, Derikx JPM, Hall N, Aldrink JH, Bailez MM, Chirdan LB, Fumino S, Hesse A, Soyer T, StPeter S, Twisk J, Yang T, van Heurn ELW; SCT-study consortium. van Heurn LJ, et al. Int J Surg. 2024 Nov 1;110(11):7177-7186. doi: 10.1097/JS9.0000000000002045. Int J Surg. 2024. PMID: 39248311 Free PMC article.

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