Kristoffersson AC - Search Results

1

Hypoaldosteronism due to a novel SEC61A1 variant successfully treated with fludrocortisone.

Karpman D, Lindström ML, Möller M, Ivarsson S, Kristoffersson AC, Bekassy Z, Fogo AB, Elfving M. Karpman D, et al. Among authors: kristoffersson ac. Clin Kidney J. 2024 Jul 5;17(8):sfae213. doi: 10.1093/ckj/sfae213. eCollection 2024 Aug. Clin Kidney J. 2024. PMID: 39135939 Free PMC article.

2

VWF-cleaving protease (ADAMTS13) in premature infants.

Hellström-Westas L, Ley D, Berg AC, Kristoffersson AC, Holmberg L. Hellström-Westas L, et al. Among authors: kristoffersson ac. Acta Paediatr. 2005 Feb;94(2):205-10. doi: 10.1111/j.1651-2227.2005.tb01892.x. Acta Paediatr. 2005. PMID: 15981755

3

von Willebrand factor mediates increased platelet retention in recurrent thrombotic thrombocytopenic purpura.

Karpman D, Lethagen S, Kristoffersson A, Isaksson C, Holmberg L. Karpman D, et al. Thromb Haemost. 1997 Dec;78(6):1456-62. Thromb Haemost. 1997. PMID: 9423794

4

Ins405AsnPro mutation in the von Willebrand factor propeptide in recessive type 2A (IIC) von Willebrand's disease.

Holmberg L, Karpman D, Isaksson C, Kristoffersson AC, Lethagen S, Schneppenheim R. Holmberg L, et al. Among authors: kristoffersson ac. Thromb Haemost. 1998 Apr;79(4):718-22. Thromb Haemost. 1998. PMID: 9569179

5

Platelet activation in hemolytic uremic syndrome.

Karpman D, Manea M, Vaziri-Sani F, Ståhl AL, Kristoffersson AC. Karpman D, et al. Among authors: kristoffersson ac. Semin Thromb Hemost. 2006 Mar;32(2):128-45. doi: 10.1055/s-2006-939769. Semin Thromb Hemost. 2006. PMID: 16575688 Review.

6

A mutation in factor I that is associated with atypical hemolytic uremic syndrome does not affect the function of factor I in complement regulation.

Nilsson SC, Karpman D, Vaziri-Sani F, Kristoffersson AC, Salomon R, Provot F, Fremeaux-Bacchi V, Trouw LA, Blom AM. Nilsson SC, et al. Among authors: kristoffersson ac. Mol Immunol. 2007 Mar;44(8):1835-44. doi: 10.1016/j.molimm.2006.10.005. Epub 2006 Nov 7. Mol Immunol. 2007. PMID: 17084897 Clinical Trial.

7

ADAMTS13 phenotype in plasma from normal individuals and patients with thrombotic thrombocytopenic purpura.

Manea M, Kristoffersson A, Tsai HM, Zhou W, Winqvist I, Oldaeus G, Billström R, Björk P, Holmberg L, Karpman D. Manea M, et al. Eur J Pediatr. 2007 Mar;166(3):249-57. doi: 10.1007/s00431-006-0354-2. Epub 2006 Dec 24. Eur J Pediatr. 2007. PMID: 17187257 Free PMC article.

8

Podocytes express ADAMTS13 in normal renal cortex and in patients with thrombotic thrombocytopenic purpura.

Manea M, Kristoffersson A, Schneppenheim R, Saleem MA, Mathieson PW, Mörgelin M, Björk P, Holmberg L, Karpman D. Manea M, et al. Br J Haematol. 2007 Sep;138(5):651-62. doi: 10.1111/j.1365-2141.2007.06694.x. Epub 2007 Jul 12. Br J Haematol. 2007. PMID: 17627784 Free article.

9

Factor H dysfunction in patients with atypical hemolytic uremic syndrome contributes to complement deposition on platelets and their activation.

Ståhl AL, Vaziri-Sani F, Heinen S, Kristoffersson AC, Gydell KH, Raafat R, Gutierrez A, Beringer O, Zipfel PF, Karpman D. Ståhl AL, et al. Among authors: kristoffersson ac. Blood. 2008 Jun 1;111(11):5307-15. doi: 10.1182/blood-2007-08-106153. Epub 2008 Feb 11. Blood. 2008. PMID: 18268093 Free article.

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. 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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