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Journal of Clinical Investigation, ISSN 0021-9738, 06/2013, Volume 123, Issue 6, pp. 2434 - 2446
Journal Article
Journal Article
NEFROLOGÍA, ISSN 0211-6995, 05/2018, Volume 38, Issue 3, pp. 258 - 266
La activación de la vía alternativa del complemento interviene en el desarrollo de varias enfermedades renales, como el síndrome hemolítico urémico atípico o... 
Acquired partial lipodystrophy | C3 glomerulopathy | C3NeF | Complemento | Complement | Glomerulopatía C3 | Lipodistrofia parcial adquirida
Journal Article
Kidney International, ISSN 0085-2538, 11/2012, Volume 82, Issue 10, pp. 1084 - 1092
Journal Article
NEFROLOGIA (English Edition), ISSN 2013-2514, 05/2018, Volume 38, Issue 3, pp. 258 - 266
The activation of the alternative pathway of the complement is involved in the development of several renal diseases, such as atypical haemolytic uraemic... 
Acquired partial lipodystrophy | C3 glomerulopathy | C3NeF | Complement | Complemento | Glomerulopatía C3 | Lipodistrofia parcial adquirida
Journal Article
Human mutation, ISSN 1059-7794, 09/2019
C1 Inhibitor (C1Inh) deficiency is responsible for hereditary angioedema (C1-INH-HAE) and caused by variants of the SERPING1/C1INH/C1NH gene. C1Inh is the... 
Journal Article
Nefrologia : publicacion oficial de la Sociedad Espanola Nefrologia, 05/2018, Volume 38, Issue 3, p. 258
The activation of the alternative pathway of the complement is involved in the development of several renal diseases, such as atypical haemolytic uremic... 
Nephritis - immunology | Complement C3 | Humans | Kidney Glomerulus | Lipodystrophy - immunology
Journal Article
NEFROLOGÍA, ISSN 0211-6995, 09/2016, Volume 36, Issue 5, pp. 489 - 495
La activación del sistema del complemento interviene en el desarrollo de varias enfermedades renales, como las glomerulonefritis mediadas por anticuerpos, el... 
Factor H | Autoantibodies | Factor B | Autoanticuerpos | C3NeF | Vía alternativa | Factor I | Alternative pathway
Journal Article
Journal Article
Orphanet Journal of Rare Diseases, ISSN 1750-1172, 2012, Volume 7, Issue 1, pp. 42 - 42
Background: Complement Factor I (CFI) is a serine protease with an important role in complement alternative pathway regulation. Complete factor I deficiency is... 
Large deletions | Complement factor I | Diagnostic flowchart | Recurrent infections | C3 consumption | Complement deficiency | MOLECULAR CHARACTERIZATION | GLOMERULONEPHRITIS | MEDICINE, RESEARCH & EXPERIMENTAL | HEMOLYTIC-UREMIC SYNDROME | FACTOR-H-AUTOANTIBODIES | INACTIVATOR | HEREDITARY | DISEASE | DYSREGULATION | GENETICS & HEREDITY | FUNCTIONAL ANALYSES | Recurrence | Exons | Humans | Genetic Diseases, Inborn - genetics | Child, Preschool | Male | Complement Factor I - deficiency | Bacterial Infections - complications | Complement C3 - deficiency | Bacterial Infections - immunology | Gene Deletion | Genetic Diseases, Inborn - complications | Adult | Female | Child | Complement C3 - genetics | Genetic Diseases, Inborn - diagnosis | Complement C4 - metabolism | Complement C3 - metabolism | Genetic Diseases, Inborn - immunology | Complement Factor I - genetics | Complement C3 - immunology | Spain | Homozygote | Pedigree | Family | Heterozygote | Mutation | Usage | Gene mutations | Complement deficiency (Immunology) | Genetic aspects | Nucleotide sequencing | Research | Diagnosis | Health aspects | Risk factors | DNA sequencing | Infection | Bacterial infections | Genes | Thrombin | Medical research | Immunoassay | Pneumonia | Disease | Infections | Manuscripts | Defects | Proteins | Studies | Genetics | Autoimmune diseases | Age
Journal Article
Journal of Allergy and Clinical Immunology, The, ISSN 0091-6749, 2008, Volume 121, Issue 2, pp. 429 - 433
Journal Article
Seminars in Cell and Developmental Biology, ISSN 1084-9521, 01/2019, Volume 85, pp. 86 - 97
The complement system is a complex and autoregulated multistep cascade at the interface of innate and adaptive immunity. It is activated by immune complexes or... 
Infection | Autoimmunity | Complement system | Molecular diagnosis | Immune deficiency | Monitoring | ECULIZUMAB | HOST-CELLS | SYSTEMIC-LUPUS-ERYTHEMATOSUS | ACTIVATION | HEMOLYTIC-UREMIC SYNDROME | C3 GLOMERULOPATHY | DEVELOPMENTAL BIOLOGY | CELL BIOLOGY | FACTOR-H AUTOANTIBODIES | MEDICAL PROGRESS | DISEASE | FUNCTIONAL-ANALYSIS
Journal Article