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Medicina Clinica|September 1, 2022
Paradigm shift in monogenic autoinflammatory diseases and systemic vasculitis: The VEXAS syndromeJosé Hernández-Rodríguez, Anna Mensa-Vilaró, Juan I Aróstegui
European Journal of Medical Genetics|March 31, 2020
Genetic diagnosis of autoinflammatory disease patients using clinical exome sequencingLaura Batlle-Masó, Anna Mensa-Vilaró, Manuel Solís-Moruno, et al.
Acta Dermato-Venereologica|August 14, 2019
Acquired Cold Urticaria vs. Autoinflammatory Diseases, Genetic and Clinical Profile and Differential Diagnosis: Study of a Cohort of Patients in a Tertiary Reference CentreGustavo Deza, Anna Mensa-Vilaró, Alvaro March-Rodriguez, et al.
Scientific Reports|June 22, 2021
Assessment of the gene mosaicism burden in blood and its implications for immune disordersManuel Solís-Moruno, Anna Mensa-Vilaró, Laura Batlle-Masó, et al.
The Australasian Journal of Dermatology|February 17, 2023
Early-onset recurrent panniculitis as a phenotype of NLRC4-associated autoinflammatory syndrome: Characterization of pathogenicity of the p.Ser445Pro NLRC4 variantJavier Gil-Lianes, Giuseppe Gariup, Pilar Iranzo-Fernández, et al.
Iscience|December 14, 2021
Low levels of <i>CIITA</i> and high levels of <i>SOCS1</i> predict COVID-19 disease severity in children and adultsMònica Girona-Alarcon, Guillermo Argüello, Ana Esteve-Sole, et al.
Clinical and Experimental Rheumatology|January 13, 2017
Novel evidences of atypical manifestations in cryopyrin-associated periodic syndromesSegundo Bujan-Rivas, Maria Basagaña, Francisca Sena, et al.
Autoimmunity Reviews|August 25, 2015
Clinical and genetic characterization of the autoinflammatory diseases diagnosed in an adult reference centerJosé Hernández-Rodríguez, Estíbaliz Ruíz-Ortiz, Adrià Tomé, et al.
Journal of Neuroimmunology|June 19, 2022
Cytokine profile and brain biopsy in a case of childhood-onset central nervous system vasculitis in Noonan syndrome-like disorder due to a novel CBL variantJuan Darío Ortigoza-Escobar, Mariona Fernández de Sevilla, Laura Monfort, et al.
Scientific Reports|March 16, 2019
Biallelic loss-of-function LACC1/FAMIN Mutations Presenting as Rheumatoid Factor-Negative Polyarticular Juvenile Idiopathic ArthritisRaquel Rabionet, Agustín Remesal, Anna Mensa-Vilaró, et al.
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