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Fernando Corvillo Rodríguez
Fernando Corvillo Rodríguez
Ph.D. in Molecular Biosciences
Verified email at idipaz.es - Homepage
Title
Cited by
Cited by
Year
Nephritic factors: an overview of classification, diagnostic tools and clinical associations
F Corvillo, M Okrój, P Nozal, M Melgosa, P Sánchez-Corral, ...
Frontiers in immunology 10, 439945, 2019
672019
Testing the activity of complement convertases in serum/plasma for diagnosis of C4NeF-mediated C3 glomerulonephritis
AM Blom, F Corvillo, M Magda, G Stasiłojć, P Nozal, MÁ Pérez-Valdivia, ...
Journal of clinical immunology 36 (5), 517-527, 2016
352016
Autoantibodies against perilipin 1 as a cause of acquired generalized lipodystrophy
F Corvillo, V Aparicio, A López-Lera, S Garrido, D Araújo-Vilar, ...
Frontiers in immunology 9, 2018
272018
Complement as a diagnostic tool in immunopathology
A López-Lera, F Corvillo, P Nozal, JR Regueiro, P Sánchez-Corral, ...
Seminars in cell & developmental biology, 2018
262018
Serum properdin consumption as a biomarker of C5 convertase dysregulation in C3 glomerulopathy
F Corvillo, M Bravo García‐Morato, P Nozal, S Garrido, A Tortajada, ...
Clinical & Experimental Immunology 184 (1), 118-125, 2016
242016
An overview of lipodystrophy and the role of the complement system
F Corvillo, B Akinci
Molecular immunology 112, 223-232, 2019
212019
Acquired partial lipodystrophy and C3 glomerulopathy: dysregulation of the complement system as a common mechanism
F Corvillo, M López-Trascasa
Nefrología (English Edition) 38 (3), 258-266, 2018
162018
Bravo García-Morato M, Nozal P, Garrido S, Tortajada A, Rodríguez de Córdoba S, et al. Serum properdin consumption as a biomarker of C5 convertase dysregulation in C3 …
F Corvillo
Clin Exp Immunol 184 (1), 118-25, 2016
142016
Complement Genetic Variants and FH Desialylation in S. pneumoniae-Haemolytic Uraemic Syndrome
I Gomez Delgado, F Corvillo, P Nozal, E Arjona, A Madrid, M Melgosa, ...
Frontiers in immunology 12, 641656, 2021
132021
Immunological features of patients affected by Barraquer-Simons syndrome
F Corvillo, G Ceccarini, P Nozal, S Magno, C Pelosini, S Garrido, ...
Orphanet journal of rare diseases 15, 1-11, 2020
122020
Complement factor d (adipsin) levels are elevated in acquired partial lipodystrophy (Barraquer–Simons syndrome)
F Corvillo, L González-Sánchez, A López-Lera, E Arjona, G Ceccarini, ...
International Journal of Molecular Sciences 22 (12), 6608, 2021
92021
The FXII c.-4T> C polymorphism as a disease modifier in patients with hereditary angioedema due to the FXII p. Thr328Lys variant
F Corvillo, ME Morena-Barrio, C Marcos-Bravo, M López-Trascasa, ...
Frontiers in Genetics 11, 1033, 2020
92020
Characterization and clinical association of autoantibodies against perilipin 1 in patients with acquired generalized lipodystrophy
F Corvillo, BS Abel, A López-Lera, G Ceccarini, S Magno, F Santini, ...
Diabetes 72 (1), 71-84, 2023
62023
Evidence of ongoing complement activation on adipose tissue from an 11‐year‐old girl with Barraquer–Simons syndrome
F Corvillo, P Nozal, A López‐Lera, MP De Miguel, JA Piñero‐Fernández, ...
The Journal of Dermatology 47 (12), 1439-1444, 2020
62020
Clinical characteristics of patients with acquired partial lipodystrophy: a multicenter retrospective study
S Magno, G Ceccarini, F Corvillo, C Pelosini, D Gilio, M Paoli, ...
The Journal of Clinical Endocrinology & Metabolism 109 (3), e932-e944, 2024
22024
Complement profile and autoantibodies against adipocytes on acquired lipodystrophies
F Corvillo, V Aparicio, S Garrido, MP de Miguel, M López-Trascasa
Abstracts/Molecular Immunology 89, 115-120, 2017
22017
Estudio de los mecanismos inmunopatológicos en lipodistrofias adquiridas de tipo parcial y generalizado
F Corvillo Rodríguez
Universidad Autónoma de Madrid, 2018
1*2018
Lipodistrofia parcial adquirida y glomerulopatía C3: la desregulación del sistema del complemento como mecanismo común
F Corvillo, M López-Trascasa
nefrologia 38 (3), 258-266, 2018
12018
Inherited Human BCL10 Deficiencies
AA Alsaidalani, B García-Solís, E Bukhari, A Van Den Rym, ...
Journal of Clinical Immunology 44 (1), 13, 2024
2024
Properdin deficiency associated with systemic meningococcal disease due to a novel p. Cys337Arg pathogenic variant
LG Sánchez, AM Agudo, A Van Den Rym, MI Begiristain, A Saizar, ...
Genes & Diseases, 101134, 2023
2023
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