Persson U - Search Results

1

Patients with Goodpasture's disease have two normal COL4A3 alleles encoding the NC1 domain of the type IV collagen alpha 3 chain.

Persson U, Hertz JM, Carlsson M, Hellmark T, Juncker I, Wieslander J, Segelmark M. Persson U, et al. Nephrol Dial Transplant. 2004 Aug;19(8):2030-5. doi: 10.1093/ndt/gfh355. Epub 2004 Jun 15. Nephrol Dial Transplant. 2004. PMID: 15199166

2

Alport syndrome in southern Sweden.

Persson U, Hertz JM, Wieslander J, Segelmark M. Persson U, et al. Clin Nephrol. 2005 Aug;64(2):85-90. doi: 10.5414/cnp64085. Clin Nephrol. 2005. PMID: 16114783

3

X-linked Alport syndrome: natural history in 195 families and genotype- phenotype correlations in males.

Jais JP, Knebelmann B, Giatras I, Marchi M, Rizzoni G, Renieri A, Weber M, Gross O, Netzer KO, Flinter F, Pirson Y, Verellen C, Wieslander J, Persson U, Tryggvason K, Martin P, Hertz JM, Schröder C, Sanak M, Krejcova S, Carvalho MF, Saus J, Antignac C, Smeets H, Gubler MC. Jais JP, et al. Among authors: persson u. J Am Soc Nephrol. 2000 Apr;11(4):649-657. doi: 10.1681/ASN.V114649. J Am Soc Nephrol. 2000. PMID: 10752524

4

Alport syndrome caused by inversion of a 21 Mb fragment of the long arm of the X-chromosome comprising exon 9 through 51 of the COL4A5 gene.

Hertz JM, Persson U, Juncker I, Segelmark M. Hertz JM, et al. Among authors: persson u. Hum Genet. 2005 Oct;118(1):23-8. doi: 10.1007/s00439-005-0013-0. Epub 2005 Oct 28. Hum Genet. 2005. PMID: 16133187

5

A candidate gene approach to ANCA-associated vasculitis reveals links to the C3 and CTLA-4 genes but not to the IL1-Ra and Fcγ-RIIa genes.

Persson U, Gullstrand B, Pettersson A, Sturfelt G, Truedsson L, Segelmark M. Persson U, et al. Kidney Blood Press Res. 2013;37(6):641-8. doi: 10.1159/000355744. Epub 2013 Dec 14. Kidney Blood Press Res. 2013. PMID: 24356554 Free article.

6

C3 and C4 allotypes in anti-neutrophil cytoplasmic autoantibody (ANCA)-positive vasculitis.

Persson U, Truedsson L, Westman KW, Segelmark M. Persson U, et al. Clin Exp Immunol. 1999 May;116(2):379-82. doi: 10.1046/j.1365-2249.1999.00889.x. Clin Exp Immunol. 1999. PMID: 10337034 Free PMC article.

7

X-linked Alport syndrome: natural history and genotype-phenotype correlations in girls and women belonging to 195 families: a "European Community Alport Syndrome Concerted Action" study.

Jais JP, Knebelmann B, Giatras I, De Marchi M, Rizzoni G, Renieri A, Weber M, Gross O, Netzer KO, Flinter F, Pirson Y, Dahan K, Wieslander J, Persson U, Tryggvason K, Martin P, Hertz JM, Schröder C, Sanak M, Carvalho MF, Saus J, Antignac C, Smeets H, Gubler MC. Jais JP, et al. Among authors: persson u. J Am Soc Nephrol. 2003 Oct;14(10):2603-10. doi: 10.1097/01.asn.0000090034.71205.74. J Am Soc Nephrol. 2003. PMID: 14514738

8

Detection of mutations in the COL4A5 gene by SSCP in X-linked Alport syndrome.

Hertz JM, Juncker I, Persson U, Matthijs G, Schmidtke J, Petersen MB, Kjeldsen M, Gregersen N. Hertz JM, et al. Among authors: persson u. Hum Mutat. 2001 Aug;18(2):141-8. doi: 10.1002/humu.1163. Hum Mutat. 2001. PMID: 11462238 Free article.

9

Citrate supplementation of PD fluid: effects on net ultrafiltration and clearance of small solutes in single dwells.

Braide M, Haraldsson B, Persson U. Braide M, et al. Among authors: persson u. Nephrol Dial Transplant. 2009 Jan;24(1):286-92. doi: 10.1093/ndt/gfn452. Epub 2008 Sep 15. Nephrol Dial Transplant. 2009. PMID: 18796439

10

Resource use and costs in a Swedish cohort of patients with Parkinson's disease.

Hagell P, Nordling S, Reimer J, Grabowski M, Persson U. Hagell P, et al. Among authors: persson u. Mov Disord. 2002 Nov;17(6):1213-20. doi: 10.1002/mds.10262. Mov Disord. 2002. PMID: 12465059

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