Nordenskjöld A - Search Results

1

Maternal Risk Factors and Perinatal Characteristics for Hirschsprung Disease.

Löf Granström A, Svenningsson A, Hagel E, Oddsberg J, Nordenskjöld A, Wester T. Löf Granström A, et al. Among authors: nordenskjold a. Pediatrics. 2016 Jul;138(1):e20154608. doi: 10.1542/peds.2015-4608. Epub 2016 Jun 15. Pediatrics. 2016. PMID: 27307146

2

Low frequency of RET mutations in Hirschsprung disease in Sweden.

Svensson PJ, Molander ML, Eng C, Anvret M, Nordenskjöld A. Svensson PJ, et al. Among authors: nordenskjold a. Clin Genet. 1998 Jul;54(1):39-44. doi: 10.1111/j.1399-0004.1998.tb03691.x. Clin Genet. 1998. PMID: 9727738

3

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. Among authors: nordenskjold a. Pediatr Res. 1999 May;45(5 Pt 1):714-7. doi: 10.1203/00006450-199905010-00018. Pediatr Res. 1999. PMID: 10231870

4

Absence of motilin gene mutations in infantile hypertrophic pyloric stenosis.

Svenningsson A, Lagerstedt K, Omrani MD, Nordenskjöld A. Svenningsson A, et al. Among authors: nordenskjold a. J Pediatr Surg. 2008 Mar;43(3):443-6. doi: 10.1016/j.jpedsurg.2007.10.006. J Pediatr Surg. 2008. PMID: 18358279

5

Maternal and gestational risk factors for hypospadias.

Akre O, Boyd HA, Ahlgren M, Wilbrand K, Westergaard T, Hjalgrim H, Nordenskjöld A, Ekbom A, Melbye M. Akre O, et al. Among authors: nordenskjold a. Environ Health Perspect. 2008 Aug;116(8):1071-6. doi: 10.1289/ehp.10791. Environ Health Perspect. 2008. PMID: 18709149 Free PMC article.

6

No association between a promoter NOS1 polymorphism (rs41279104) and Infantile Hypertrophic Pyloric Stenosis.

Lagerstedt-Robinson K, Svenningsson A, Nordenskjöld A. Lagerstedt-Robinson K, et al. Among authors: nordenskjold a. J Hum Genet. 2009 Dec;54(12):706-8. doi: 10.1038/jhg.2009.101. Epub 2009 Oct 23. J Hum Genet. 2009. PMID: 19851341

7

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: nordenskjold a. J Pediatr Surg. 2011 Jul;46(7):1390-5. doi: 10.1016/j.jpedsurg.2011.02.039. J Pediatr Surg. 2011. PMID: 21763840

8

Genome-wide linkage analysis in families with infantile hypertrophic pyloric stenosis indicates novel susceptibility loci.

Svenningsson A, Söderhäll C, Persson S, Lundberg F, Luthman H, Chung E, Gardiner M, Kockum I, Nordenskjöld A. Svenningsson A, et al. Among authors: nordenskjold a. J Hum Genet. 2012 Feb;57(2):115-21. doi: 10.1038/jhg.2011.137. Epub 2011 Dec 8. J Hum Genet. 2012. PMID: 22158425

9

Novel mutations in the MNX1 gene in two families with Currarino syndrome and variable phenotype.

Markljung E, Adamovic T, Cao J, Naji H, Kaiser S, Wester T, Nordenskjöld A. Markljung E, et al. Among authors: nordenskjold a. Gene. 2012 Oct 1;507(1):50-3. doi: 10.1016/j.gene.2012.06.096. Epub 2012 Jul 20. Gene. 2012. PMID: 22820079

10

A rare microduplication in a familial case of annular pancreas and duodenal stenosis.

Markljung E, Adamovic T, Ortqvist L, Wester T, Nordenskjöld A. Markljung E, et al. Among authors: nordenskjold a. J Pediatr Surg. 2012 Nov;47(11):2039-43. doi: 10.1016/j.jpedsurg.2012.06.028. J Pediatr Surg. 2012. PMID: 23163995

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