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 | 67 | 2019 |
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 | 35 | 2016 |
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 | 27 | 2018 |
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 | 26 | 2018 |
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 | 24 | 2016 |
An overview of lipodystrophy and the role of the complement system F Corvillo, B Akinci Molecular immunology 112, 223-232, 2019 | 21 | 2019 |
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 | 16 | 2018 |
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 | 14 | 2016 |
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 | 13 | 2021 |
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 | 12 | 2020 |
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 | 9 | 2021 |
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 | 9 | 2020 |
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 | 6 | 2023 |
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 | 6 | 2020 |
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 | 2 | 2024 |
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 | 2 | 2017 |
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 | 1 | 2018 |
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 |