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au.\*:("KARPMAN, Diana")

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Results 1 to 21 of 21

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Kinin system activation in vasculitisKAHN, Robin; KARPMAN, Diana.Acta paediatrica (Oslo). 2011, Vol 100, Num 7, pp 950-957, issn 0803-5253, 8 p.Article

Human renal epithelial cells express iNOS in response to cytokines but not bacteriaPOLJAKOVIC, Mirjana; KARPMAN, Diana; SVANBORG, Catharina et al.Kidney international. 2002, Vol 61, Num 2, pp 444-455, issn 0085-2538Article

Shiga Toxin Pathogenesis: Kidney Complications and Renal FailureOBRIG, Tom G; KARPMAN, Diana.Current Topics in Microbiology and Immunology. 2012, Vol 357, pp 105-136, issn 0070-217X, 32 p.Article

Antibody response to IgA-binding streptococcal M proteins in children with IgA nephropathySCHMITT, Roland; LINDAHL, Gunnar; KARPMAN, Diana et al.Nephrology, dialysis, transplantation (Print). 2010, Vol 25, Num 10, pp 3434-3436, issn 0931-0509, 3 p.Article

Cross-Reactive Protection against Enterohemorrhagic Escherichia coli Infection by Enteropathogenic E. coli in a Mouse ModelCALDERON TOLEDO, Carla; ARVIDSSON, Ida; KARPMAN, Diana et al.Infection and immunity. 2011, Vol 79, Num 6, pp 2224-2233, issn 0019-9567, 10 p.Article

Pathogenesis of Shiga toxin-associated hemolytic uremic syndromePROULX, Francois; SEIDMAN, Ernest G; KARPMAN, Diana et al.Pediatric research. 2001, Vol 50, Num 2, pp 163-171, issn 0031-3998Article

Correct evaluation of renal glomerular filtration rate requires clearance assaysHJORTH, Lars; WIEBE, Thomas; KARPMAN, Diana et al.Pediatric nephrology (Berlin, West). 2002, Vol 17, Num 10, pp 847-851, issn 0931-041XArticle

Anguish over angiopathy : Hemolytic uremic syndromeKARPMAN, Diana; BLOM, Anna; GOODSHIP, Timothy et al.Clinical immunology (Orlando, Fla. Print). 2007, Vol 122, Num 2, pp 135-138, issn 1521-6616, 4 p.Article

IgA nephropathy associated with a novel N-terminal mutation in factor HSCHMITT, Roland; KRMAR, Rafael T; KRISTOFFERSSON, Anncharlotte et al.European journal of pediatrics. 2011, Vol 170, Num 1, pp 107-110, issn 0340-6199, 4 p.Article

Pathophysiology of Typical Hemolytic Uremic SyndromeKARPMAN, Diana; SARTZ, Lisa; JOHNSON, Sally et al.Seminars in thrombosis and hemostasis. 2010, Vol 36, Num 6, pp 575-585, issn 0094-6176, 11 p.Article

Tissue Deposits of IgA-Binding Streptococcal M Proteins in IgA Nephropathy and Henoch-Schönlein PurpuraSCHMITT, Roland; CARLSSON, Fredric; MÖRGELIN, Matthias et al.The American journal of pathology. 2010, Vol 176, Num 2, pp 608-618, issn 0002-9440, 11 p.Article

Contact-system activation in children with vasculitisKAHN, Robin; HERWALD, Heiko; MÜLLER-ESTERL, Werner et al.Lancet (British edition). 2002, Vol 360, Num 9332, pp 535-541, issn 0140-6736Article

Lipopolysaccharide from enterohemorrhagic Escherichia coli binds to platelets through TLR4 and CD62 and is detected on circulating platelets in patients with hemolytic uremic syndromeSTAHL, Anne-Lie; SVENSSON, Majlis; MÖRGELIN, Matthias et al.Blood. 2006, Vol 108, Num 1, pp 167-176, issn 0006-4971, 10 p.Article

ADAMTS13 phenotype in plasma from normal individuals and patients with thrombotic thrombocytopenic purpuraMANEA, Minola; KRISTOFFERSSON, Anncharlotte; TSAI, Han-Mou et al.European journal of pediatrics. 2007, Vol 166, Num 3, pp 249-257, issn 0340-6199, 9 p.Article

Uropathogenic Escherichia coli as a model of host-parasite interactionSVANBORG, Catharina; BERGSTEN, Göran; FISCHER, Hans et al.Current opinion in microbiology. 2006, Vol 9, Num 1, pp 33-39, issn 1369-5274, 7 p.Article

Platelet activation in hemolytic uremic syndromeKARPMAN, Diana; MANEA, Minola; VAZIRI-SANI, Fariba et al.Seminars in thrombosis and hemostasis. 2006, Vol 32, Num 2, pp 128-145, issn 0094-6176, 18 p.Article

Mutation analysis and clinical implications of von Willebrand factor-cleaving protease deficiencyASSINK, Karin; SCHIPHORST, Rikke; ALLFORD, Sarah et al.Kidney international. 2003, Vol 63, Num 6, pp 1995-1999, issn 0085-2538, 5 p.Article

Thrombotic microangiopathy mimicking membranoproliferative glomerulonephritisBRACKMAN, Damien; SARTZ, Lisa; LEH, Sabine et al.Nephrology, dialysis, transplantation (Print). 2011, Vol 26, Num 10, pp 3399-3403, issn 0931-0509, 5 p.Article

Factor H dysfunction in patients with atypical hemolytic uremic syndrome contributes to complement deposition on platelets and their activation. CommentaryAFSHAR-KHARGHAN, Vahid; STAHL, Anne-Lie; KARPMAN, Diana et al.Blood. 2008, Vol 111, Num 11, issn 0006-4971, 5266, 5307-5315 [10 p.]Article

Podocytes express ADAMTS13 in normal renal cortex and in patients with thrombotic thrombocytopenic purpuraMANEA, Minola; KRISTOFFERSSON, Anncharlotte; SCHNEPPENHEIM, Reinhard et al.British journal of haematology. 2007, Vol 138, Num 5, pp 651-662, issn 0007-1048, 12 p.Article

Antibodies to intimin and Escherichia coli secreted proteins A and B in patients with enterohemorrhagic Escherichia coli infectionsKARPMAN, Diana; BEKASSY, Zivile D; KAPER, James B et al.Pediatric nephrology (Berlin, West). 2002, Vol 17, Num 3, pp 201-211, issn 0931-041XArticle

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