受强制性开放获取政策约束的文章 - Christoph Licht了解详情
无法在其他位置公开访问的文章：9 篇
DEAP-HUS: deficiency of CFHR plasma proteins and autoantibody-positive form of hemolytic uremic syndrome
PF Zipfel, C Mache, D Müller, C Licht, M Wigger, C Skerka, ...
Pediatric nephrology 25, 2009-2019, 2010
强制性开放获取政策： Heart and Stroke Foundation of Canada, German Research Foundation
Pathological aspects of membranoproliferative glomerulonephritis (MPGN) and haemolytic uraemic syndrome (HUS)/thrombocytic thrombopenic purpura (TTP)
K Benz, K Amann
Thrombosis and haemostasis 101 (02), 265-270, 2009
强制性开放获取政策： German Research Foundation
Autoimmune forms of thrombotic micorangiopathy and membranoproliferative glomerulonephritis: Indications for a disease spectrum and common pathogenic principles
C Skerka, C Licht, M Mengel, B Uzonyi, S Strobel, PF Zipfel, M Józsi
Molecular immunology 46 (14), 2801-2807, 2009
强制性开放获取政策： German Research Foundation
Pretransplant genetic susceptibility: clinical relevance in transplant-associated thrombotic microangiopathy
E Gavriilaki, T Touloumenidou, I Sakellari, I Batsis, D Mallouri, ...
Thrombosis and haemostasis 120 (04), 638-646, 2020
强制性开放获取政策： European Hematology Association, Netherlands
The role of defective complement control in hemolytic uremic syndrome
C Licht, C Skerka, J Misselwitz, PF Zipfel
Seminars in thrombosis and hemostasis 32 (02), 146-154, 2006
强制性开放获取政策： German Research Foundation
Genetic and Functional Characterization of ADAMTS13 Variants in a Patient Cohort with Upshaw–Schulman Syndrome Investigated in Germany
WA Hassenpflug, T Obser, J Bode, F Oyen, U Budde, S Schneppenheim, ...
Thrombosis and Haemostasis 118 (04), 709-722, 2018
强制性开放获取政策： German Research Foundation
Long-term data on two sisters with C3GN due to an identical, homozygous CFH mutation and autoantibodies
A Hackl, F Erger, C Skerka, A Wenzel, N Tschernoster, R Ehren, ...
Clinical Nephrology 94 (4), 197, 2020
强制性开放获取政策： German Research Foundation
Lack of Complement Factor H Contributes to Endothelial Cell Injury in Shiga Toxin Haemolytic Uraemic Syndrome: FR-PO715
EE Bowen, J Hurcombe, F Barrington, LK Farmer, CG Ortiz-Sandoval, ...
Journal of the American Society of Nephrology 33 (11S), 518, 2022
强制性开放获取政策： US National Institutes of Health
Langzeitdaten von zwei Schwestern mit C3-Glomerulonephritis (C3-GN) aufgrund einer homozygoten CFH-Mutation und Auto-Antikörpern
A Hackl, F Erger, C Skerka, A Wenzel, N Tschernoster, R Ehren, ...
Nieren-und Hochdruckkrankheiten 50 (7), 282, 2021
强制性开放获取政策： German Research Foundation
可在其他位置公开访问的文章：50 篇
Atypical hemolytic uremic syndrome and C3 glomerulopathy: conclusions from a “Kidney Disease: Improving Global Outcomes”(KDIGO) Controversies Conference
THJ Goodship, HT Cook, F Fakhouri, FC Fervenza, V Frémeaux-Bacchi, ...
Kidney international 91 (3), 539-551, 2017
强制性开放获取政策： UK Medical Research Council, Wellcome Trust
Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test
AC Lionel, G Costain, N Monfared, S Walker, MS Reuter, SM Hosseini, ...
Genetics in Medicine 20 (4), 435-443, 2018
强制性开放获取政策： Canadian Institutes of Health Research, Genome Canada
Efficacy and safety of eculizumab in atypical hemolytic uremic syndrome from 2-year extensions of phase 2 studies
C Licht, LA Greenbaum, P Muus, S Babu, CL Bedrosian, DJ Cohen, ...
Kidney international 87 (5), 1061-1073, 2015
强制性开放获取政策： US National Institutes of Health
Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency
M Józsi, C Licht, S Strobel, SLH Zipfel, H Richter, S Heinen, PF Zipfel, ...
Blood, The Journal of the American Society of Hematology 111 (3), 1512-1514, 2008
强制性开放获取政策： German Research Foundation
Deletion of Complement Factor H–Related Genes CFHR1 and CFHR3 Is Associated with Atypical Hemolytic Uremic Syndrome
PF Zipfel, M Edey, S Heinen, M Józsi, H Richter, J Misselwitz, B Hoppe, ...
PLoS genetics 3 (3), e41, 2007
强制性开放获取政策： German Research Foundation
Abnormalities in the alternative pathway of complement in children with hematopoietic stem cell transplant-associated thrombotic microangiopathy
S Jodele, C Licht, J Goebel, BP Dixon, K Zhang, TA Sivakumaran, ...
Blood, The Journal of the American Society of Hematology 122 (12), 2003-2007, 2013
强制性开放获取政策： US National Institutes of Health
Deletion of Lys224 in regulatory domain 4 of Factor H reveals a novel pathomechanism for dense deposit disease (MPGN II)
C Licht, S Heinen, M Jozsi, I Löschmann, RE Saunders, SJ Perkins, ...
Kidney international 70 (1), 42-50, 2006
强制性开放获取政策： German Research Foundation
Eculizumab therapy in children with severe hematopoietic stem cell transplantation–associated thrombotic microangiopathy
S Jodele, T Fukuda, A Vinks, K Mizuno, BL Laskin, J Goebel, BP Dixon, ...
Biology of Blood and Marrow Transplantation 20 (4), 518-525, 2014
强制性开放获取政策： US National Institutes of Health
Identification of a rare coding variant in complement 3 associated with age-related macular degeneration
X Zhan, DE Larson, C Wang, DC Koboldt, YV Sergeev, RS Fulton, ...
Nature genetics 45 (11), 1375-1379, 2013
强制性开放获取政策： US National Institutes of Health, National Health and Medical Research …
Outrageous prices of orphan drugs: a call for collaboration
L Luzzatto, HI Hyry, A Schieppati, E Costa, S Simoens, F Schaefer, ...
The Lancet 392 (10149), 791-794, 2018
强制性开放获取政策： Research Foundation (Flanders)
NETosing Neutrophils Activate Complement Both on Their Own NETs and Bacteria via Alternative and Non-alternative Pathways
J Yuen, FG Pluthero, DN Douda, M Riedl, A Cherry, M Ulanova, ...
Frontiers in immunology 7, 137, 2016
强制性开放获取政策： Canadian Institutes of Health Research, Natural Sciences and Engineering …
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