Results 111 to 120 of about 24,964 (213)

Eculizumab in C3 Glomerulopathy: A Systematic Review of Therapeutic Efficacy and Clinical Outcomes

Pharmaceutics
Background: C3 glomerulopathies (C3G), including dense deposit disease (DDD) and C3 glomerulonephritis (C3GN), are rare kidney disorders driven by dysregulation of the alternative complement pathway.
Dominik Lewandowski, Mateusz Konieczny, Krzysztof Chrzanowski, Marta Jakubowska, Zuzanna Paryzek, Miłosz Miedziaszczyk, Ilona Idasiak-Piechocka   +6 more
doaj   +1 more source

Recurrent C3 Glomerulonephritis along with BK-Virus-Associated Nephropathy after Kidney Transplantation: A Case Report. [PDF]

Medicina (Kaunas), 2023
Lim JH, Shin SW, Kim MS, Han MH, Kim YJ, Jung HY, Choi JY, Cho JH, Park SH, Kim YL, Hwang D, Yun WS, Kim HK, Huh S, Yoo ES, Won DI, Kim CD.   +16 more
europepmc   +1 more source

Annus Mirabilis - a guide to the 6th European Lupus meeting 3-5 March 2005 [PDF]

, 2005
This article has no ...
Bowman, S.J., Giles, I.P., Ioannou, Y., Isenburg, D.A., Rahman, A.   +4 more
core  

Renal injury in scleromyxoedema due to monoclonal gammopathy associated C3 glomerulonephritis. [PDF]

BMJ Case Rep, 2022
Kao S, Silinsky Krupnikova SD, AlMackenzie M, Atefi G.   +3 more
europepmc   +1 more source

World small animal veterinary association renal pathology initiative: classification of glomerular diseases in dogs [PDF]

, 2015
Aresu, L, Brovida, C, Brown, C A, Cianciolo, R E, Cowgill, L D, Heiene, R, James, C, Jansen, J H, Kass, PH, Lees, G E, Mohr, F C, Polzin, D J, Spangler, W L, Syme, H M, Vaden, S L, van de Lugt, JJ, van Dongen, A M   +16 more
core   +2 more sources

Anti-C1q autoantibodies do not correlate with the occurrence or severity of experimental lupus nephritis [PDF]

, 2017
Background. In systemic lupus erythematosus patients, a strong association between the occurrence of antibodies against complement C1q (anti-C1q) and lupus nephritis can be observed.
Bigler, Cornelia, Danner, Doris, Hopfer, Helmut, Mihatsch, Michael J., Schaller, Monica, Trendelenburg, Marten   +5 more
core  

Hereditary complement factor I deficiency [PDF]

, 2017
Summary We describe four cases (from three families) of hereditary factor I deficiency, bringing the total number of cases now reported to 23. In one family there are two affected siblings: one has suffered recurrent pyogenic infections; the other is ...
ATHANASSIOU, P., DAVIES, K.A., GILES, C.M., MORLEY, B.J., PHILIPPE, P., SPÄTH, P.J., VYSE, T.J., WALPORT, M.J.   +7 more
core  

C3 glomerulonephritis associated with ANCA positivity: a case report. [PDF]

BMC Nephrol, 2021
Li L, Liu LQ, Yang YY, Hu ZX.
europepmc   +1 more source

Diagnostic and therapeutic challenges in dense deposit disease: case report

Počki
We report a complex case of a 15-year-old girl initially diagnosed with post-streptococcal glomerulonephritis (PSGN) but later identified as having dense deposit disease, which was initially classified as type 2 membranoproliferative glomerulonephritis ...
Anand Prasad, Dhruv Jain, Navya Jaiswal, Harsha Shahi   +3 more
doaj   +1 more source

Endocardite Aguda Bi-Valvular Esquerda por Estafilococo Aureus Meticilino-Resistente com Complicações Cardíaca, Cerebral, Renal e Sepsis [PDF]

, 2011
Infective endocarditis (IE) is now rare in developed countries, but its prevalence is higher in elderly patients with prosthetic valves, diabetes, renal impairment, or heart failure.
Carvalho, F, Damásio, H, Figueiredo, M, Gomes, P, Murinello, A, Peres, H, Póvoas, D, Ramos, A, Rodrigues, N, Sousa, J   +9 more
core