Reduced membrane attack complex formation in umbilical cord blood during Eculizumab treatment of the mother: a case report
暂无分享,去创建一个
M. Tepel | C. Nielsen | Y. Palarasah | C. Bistrup | L. Andersen | K. Assing | S. Nagarajah | L. Lange
[1] J. Wetzels,et al. Living Donor Kidney Transplantation in Atypical Hemolytic Uremic Syndrome: A Case Series. , 2017, American journal of kidney diseases : the official journal of the National Kidney Foundation.
[2] J. Wetzels,et al. Eculizumab Dosing Regimen in Atypical HUS: Possibilities for Individualized Treatment , 2017, Clinical pharmacology and therapeutics.
[3] G. Remuzzi,et al. Outcomes of patients with atypical haemolytic uraemic syndrome with native and transplanted kidneys treated with eculizumab: a pooled post hoc analysis , 2017, Transplant international : official journal of the European Society for Organ Transplantation.
[4] J. Nezu,et al. Long lasting neutralization of C5 by SKY59, a novel recycling antibody, is a potential therapy for complement-mediated diseases , 2017, Scientific Reports.
[5] L. Salomon,et al. Atypical haemolytic uraemic syndrome and pregnancy: outcome with ongoing eculizumab. , 2016, Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association.
[6] J. Arredondo,et al. Blood SC5b-9 complement levels increase at parturition during term and preterm labor. , 2015, Journal of reproductive immunology.
[7] J. Andersen,et al. Eculizumab treatment during pregnancy does not affect the complement system activity of the newborn. , 2015, Immunobiology.
[8] G. Remuzzi,et al. Efficacy and safety of eculizumab in atypical hemolytic uremic syndrome from 2-year extensions of phase 2 studies , 2015, Kidney international.
[9] D. Kavanagh,et al. Anticomplement C5 therapy with eculizumab for the treatment of paroxysmal nocturnal hemoglobinuria and atypical hemolytic uremic syndrome. , 2015, Translational research : the journal of laboratory and clinical medicine.
[10] D. Kavanagh,et al. Atypical Hemolytic Uremic Syndrome , 2013, Seminars in nephrology.
[11] A. Malek. Role of IgG antibodies in association with placental function and immunologic diseases in human pregnancy , 2013, Expert review of clinical immunology.
[12] K. Skjødt,et al. Novel assays to assess the functional capacity of the classical, the alternative and the lectin pathways of the complement system , 2011, Clinical and experimental immunology.
[13] K. Skjødt,et al. Generation of a C3c specific monoclonal antibody and assessment of C3c as a putative inflammatory marker derived from complement factor C3. , 2010, Journal of immunological methods.
[14] J. Goodship,et al. Deletion of Complement Factor H–Related Genes CFHR1 and CFHR3 Is Associated with Atypical Hemolytic Uremic Syndrome , 2007, PLoS genetics.
[15] Econor,et al. ANNEX I SUMMARY OF PRODUCT CHARACTERISTICS , 2002 .