Keyphrases
Advanced Age-related Macular Degeneration
31%
Age-related Macular Degeneration
33%
Alternative Pathway
14%
Atypical Hemolytic Uremic Syndrome (aHUS)
88%
Autoimmune Disease
15%
C3 Glomerulopathy
25%
CD46
11%
Complement Activation
54%
Complement Cascade
14%
Complement Dysregulation
16%
Complement Factor H
42%
Complement Factors
44%
Complement Pathway
11%
Complement Proteins
19%
Complement Receptors
28%
Complement Regulators
12%
Complement System
51%
COVID-19
11%
Cytomegalovirus
11%
Disease-associated
13%
Dysregulated
11%
Early Onset Drusen
11%
Eculizumab
26%
Epithelial Cells
11%
Functional Analysis
14%
Functional Assay
11%
Genetic Progression
11%
Genetic Studies
11%
Genetic Variants
48%
Idiopathic Membranous Nephropathy
11%
Kidney
28%
Kidney Transplant
12%
Kidney Transplantation
22%
Management Strategy
33%
Membranous Nephropathy
11%
Missense Variants
12%
Pathophysiology
12%
Perioperative Evaluation
11%
Postpartum Period
11%
Preeclampsia
16%
Pregnancy Disorders
13%
Quality of Life Impact
11%
Rare Genetic Variants
11%
Rare Variants
13%
Renal Disease
18%
Renal Transplant
13%
Thrombotic Microangiopathy
100%
Treatment Preferences
11%
Treatment Quality
11%
Variants of Uncertain Significance
17%
Medicine and Dentistry
Age Related Macular Degeneration
19%
Allograft
5%
Antigen Antibody Complex
8%
Antiphospholipid Syndrome
7%
Atypical Hemolytic Uremic Syndrome
70%
Autoantibodies
7%
Autoimmune Disease
14%
Complement Activation
38%
Complement Factor H
14%
Complement Factor I
22%
Complement Inhibitor
6%
Complement Regulator
11%
Complement System
38%
COVID-19
11%
Creatinine
7%
Cytomegalovirus
11%
Diagnosis
12%
Disease
10%
Diseases
46%
Eculizumab
26%
Elevated Transaminases
11%
End Organ Damage
8%
End Stage Renal Disease
11%
Endothelial Cell
7%
Genetic Variability
7%
Geographic Atrophy
6%
Glomerulopathy
21%
Immunity
7%
Infusion
7%
Innate Immunity
7%
Kidney Disorder
7%
Kidney Graft
34%
Kidney Transplantation
22%
Lactate Dehydrogenase
7%
Low Platelet Count
11%
Membrane Cofactor Protein
14%
Membranoproliferative Glomerulonephritis
11%
Membranous Glomerulonephritis
11%
Microangiopathy
25%
Nephropathy
14%
Pathophysiology
14%
Protein Deficiency
5%
Puerperium
11%
Quality of Life
11%
Ravulizumab
11%
Recurrent Disease
7%
Systemic Lupus Erythematosus
9%
Thrombosis
8%
Thrombotic Thrombocytopenic Purpura
93%
Transplantation
12%
Immunology and Microbiology
Autoimmune Disease
14%
Autoimmunity
6%
Blood Plasma
7%
C3b
6%
CD46
14%
Complement Activation
41%
Complement Disorder
11%
Complement Factor
11%
Complement Factor B
6%
Complement Factor I
22%
Complement Inhibitor
5%
Complement Receptor 1
26%
Complement Regulator
12%
Complement System
33%
COVID-19
11%
Eclampsia
11%
Factor H
36%
Fibrinogen
21%
Humoral Immunity
5%
Immunity
9%
Infectious Agent
6%
Inflammation Response
7%
Innate Immune System
5%
Kidney Transplantation
11%
Membranous Glomerulonephritis
11%
Podocyte
6%
Thrombotic Thrombocytopenic Purpura
33%
Wild Type
14%