Karpman D - Search Results

1

A classification of hemolytic uremic syndrome and thrombotic thrombocytopenic purpura and related disorders.

Besbas N, Karpman D, Landau D, Loirat C, Proesmans W, Remuzzi G, Rizzoni G, Taylor CM, Van de Kar N, Zimmerhackl LB; European Paediatric Research Group for HUS. Besbas N, et al. Among authors: karpman d. Kidney Int. 2006 Aug;70(3):423-31. doi: 10.1038/sj.ki.5001581. Epub 2006 Jun 14. Kidney Int. 2006. PMID: 16775594 Free article. Review.

2

Complement dysregulation associated with a genetic variant in factor H-related protein 5 in atypical hemolytic uremic syndrome.

Aradottir SS, Kristoffersson AC, Linnér E, Karpman D. Aradottir SS, et al. Among authors: karpman d. Pediatr Nephrol. 2024 Apr;39(4):1105-1111. doi: 10.1007/s00467-023-06184-6. Epub 2023 Nov 13. Pediatr Nephrol. 2024. PMID: 37955705 Free PMC article.

3

In Vivo Sustained Release of the Retrograde Transport Inhibitor Retro-2.1 Formulated in a Thermosensitive Hydrogel.

Vinck R, Nguyen LA, Munier M, Caramelle L, Karpman D, Barbier J, Pruvost A, Cintrat JC, Gillet D. Vinck R, et al. Among authors: karpman d. Int J Mol Sci. 2022 Nov 23;23(23):14611. doi: 10.3390/ijms232314611. Int J Mol Sci. 2022. PMID: 36498939 Free PMC article.

4

Increased platelet retention in familial recurrent thrombotic thrombocytopenic purpura.

Karpman D, Holmberg L, Jirgård L, Lethagen S. Karpman D, et al. Kidney Int. 1996 Jan;49(1):190-9. doi: 10.1038/ki.1996.26. Kidney Int. 1996. PMID: 8770967 Free article.

5

Mutation analysis and clinical implications of von Willebrand factor-cleaving protease deficiency.

Assink K, Schiphorst R, Allford S, Karpman D, Etzioni A, Brichard B, van de Kar N, Monnens L, van den Heuvel L. Assink K, et al. Among authors: karpman d. Kidney Int. 2003 Jun;63(6):1995-9. doi: 10.1046/j.1523-1755.63.6s.1.x. Kidney Int. 2003. PMID: 12753286 Free article.

6

Phenotypic expression of factor H mutations in patients with atypical hemolytic uremic syndrome.

Vaziri-Sani F, Holmberg L, Sjöholm AG, Kristoffersson AC, Manea M, Frémeaux-Bacchi V, Fehrman-Ekholm I, Raafat R, Karpman D. Vaziri-Sani F, et al. Among authors: karpman d. Kidney Int. 2006 Mar;69(6):981-8. doi: 10.1038/sj.ki.5000155. Kidney Int. 2006. PMID: 16528247 Free article.

7

Epidemiology, clinical presentation, and pathophysiology of atypical and recurrent hemolytic uremic syndrome.

Zimmerhackl LB, Besbas N, Jungraithmayr T, van de Kar N, Karch H, Karpman D, Landau D, Loirat C, Proesmans W, Prüfer F, Rizzoni G, Taylor MC; European Study Group for Haemolytic Uraemic Syndromes and Related Disorders. Zimmerhackl LB, et al. Among authors: karpman d. Semin Thromb Hemost. 2006 Mar;32(2):113-20. doi: 10.1055/s-2006-939767. Semin Thromb Hemost. 2006. PMID: 16575686

8

Characterization of mutations in complement factor I (CFI) associated with hemolytic uremic syndrome.

Kavanagh D, Richards A, Noris M, Hauhart R, Liszewski MK, Karpman D, Goodship JA, Fremeaux-Bacchi V, Remuzzi G, Goodship TH, Atkinson JP. Kavanagh D, et al. Among authors: karpman d. Mol Immunol. 2008 Jan;45(1):95-105. doi: 10.1016/j.molimm.2007.05.004. Epub 2007 Jun 26. Mol Immunol. 2008. PMID: 17597211

9

Guideline for the investigation and initial therapy of diarrhea-negative hemolytic uremic syndrome.

Ariceta G, Besbas N, Johnson S, Karpman D, Landau D, Licht C, Loirat C, Pecoraro C, Taylor CM, Van de Kar N, Vandewalle J, Zimmerhackl LB; European Paediatric Study Group for HUS. Ariceta G, et al. Among authors: karpman d. Pediatr Nephrol. 2009 Apr;24(4):687-96. doi: 10.1007/s00467-008-0964-1. Epub 2008 Sep 18. Pediatr Nephrol. 2009. PMID: 18800230

10

A novel mutation in the complement regulator clusterin in recurrent hemolytic uremic syndrome.

Ståhl AL, Kristoffersson A, Olin AI, Olsson ML, Roodhooft AM, Proesmans W, Karpman D. Ståhl AL, et al. Among authors: karpman d. Mol Immunol. 2009 Jul;46(11-12):2236-43. doi: 10.1016/j.molimm.2009.04.012. Epub 2009 May 15. Mol Immunol. 2009. PMID: 19446882

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