Margarita Trascasa-Lopez

Madrid, MD, Spain

Last Updated: 09/26/2026

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Found 62 publications

Common and rare variants in complement genes as biomarkers of COVID-19 infection and severity. A lesson to learn for emerging pathogens.

Common and rare variants in complement genes as biomarkers of COVID-19 infection and severity. A lesson to learn for emerging pathogens.

Journal: Frontiers in immunology

Published: March 12, 2026

Primary Amoebic Meningoencephalitis caused by Complement C2 Deficiency.

Primary Amoebic Meningoencephalitis caused by Complement C2 Deficiency.

Journal: medRxiv : the preprint server for health sciences

Published: February 12, 2026

Serum adipsin levels in rheumatic diseases: defining its role in disease activity and progression in rheumatoid arthritis and axial spondyloarthritis.

Serum adipsin levels in rheumatic diseases: defining its role in disease activity and progression in rheumatoid arthritis and axial spondyloarthritis.

Journal: Frontiers in immunology

Published: May 27, 2025

Genetic determinants of the complement and coagulation pathways in invasive meningococcal disease.

Genetic determinants of the complement and coagulation pathways in invasive meningococcal disease.

Journal: The Journal of allergy and clinical immunology

Published: March 28, 2025

Perilipin-1 autoantibodies are a robust marker of acquired lipodystrophy and may precede clinical detection.

Perilipin-1 autoantibodies are a robust marker of acquired lipodystrophy and may precede clinical detection.

Journal: Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology

Published: October 23, 2024

Clinical Characteristics of Patients With Acquired Partial Lipodystrophy: A Multicenter Retrospective Study.

Clinical Characteristics of Patients With Acquired Partial Lipodystrophy: A Multicenter Retrospective Study.

Journal: The Journal of clinical endocrinology and metabolism

Published: July 14, 2023

Properdin deficiency associated with systemic meningococcal disease due to a novel p.Cys337Arg pathogenic variant.

Properdin deficiency associated with systemic meningococcal disease due to a novel p.Cys337Arg pathogenic variant.

Journal: Genes & diseases

Published: July 03, 2023

SERPING1 Variants and C1-INH Biological Function: A Close Relationship With C1-INH-HAE.

SERPING1 Variants and C1-INH Biological Function: A Close Relationship With C1-INH-HAE.

Journal: Frontiers in allergy

Published: December 14, 2021

Characterization and Clinical Association of Autoantibodies Against Perilipin 1 in Patients With Acquired Generalized Lipodystrophy.

Characterization and Clinical Association of Autoantibodies Against Perilipin 1 in Patients With Acquired Generalized Lipodystrophy.

Journal: Diabetes

Published: November 30, 2021

Case Report: Combined Liver-Kidney Transplantation to Correct a Mutation in Complement Factor B in an Atypical Hemolytic Uremic Syndrome Patient.

Case Report: Combined Liver-Kidney Transplantation to Correct a Mutation in Complement Factor B in an Atypical Hemolytic Uremic Syndrome Patient.

Journal: Frontiers in immunology

Published: July 31, 2021

Complement Factor D (adipsin) Levels Are Elevated in Acquired Partial Lipodystrophy (Barraquer-Simons syndrome).

Complement Factor D (adipsin) Levels Are Elevated in Acquired Partial Lipodystrophy (Barraquer-Simons syndrome).

Journal: International journal of molecular sciences

Published: May 07, 2021

Thrombin in the Activation of the Fluid Contact Phase in Patients with Hereditary Angioedema Carrying the F12 P.Thr309Lys Variant.

Thrombin in the Activation of the Fluid Contact Phase in Patients with Hereditary Angioedema Carrying the F12 P.Thr309Lys Variant.

Journal: Clinical reviews in allergy & immunology

Published: January 13, 2021

Showing 1-12 of 62

Last Updated: 09/26/2026