JOSÉ LUIS
CALLEJAS RUBIO
PROFESOR PERMANENTE LABORAL
Hospital Clinic Barcelona
Barcelona, EspañaPublicaciones en colaboración con investigadores/as de Hospital Clinic Barcelona (20)
2024
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Autoimmune and Rheumatic Diseases and Sexuality
Trends in Andrology and Sexual Medicine (Springer Science and Business Media Deutschland GmbH), pp. 291-304
2023
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External clinical validation of automated software to identify structural abnormalities and microhaemorrhages in nailfold videocapillaroscopy images
Clinical and experimental rheumatology, Vol. 41, Núm. 8, pp. 1605-1611
2022
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Complement component C4 structural variation and quantitative traits contribute to sex-biased vulnerability in systemic sclerosis
npj Genomic Medicine, Vol. 7, Núm. 1
2021
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Multidisciplinary care and units for uveitis in the internal medicine departments in Spain: Survey of the Systemic Autoimmune Diseases Group
Revista Clinica Espanola, Vol. 221, Núm. 4, pp. 221-225
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SARS-CoV-2 infection in patients with primary Sjögren syndrome: Characterization and outcomes of 51 patients
Rheumatology (United Kingdom), Vol. 60, Núm. 6, pp. 2946-2957
2020
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A cross-disease meta-GWAS identifies four new susceptibility loci shared between systemic sclerosis and Crohn’s disease
Scientific Reports, Vol. 10, Núm. 1
2019
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LAUDES Study: impact of digital ulcers on hand functional limitation, work productivity and daily activities, in systemic sclerosis patients
Rheumatology International, Vol. 39, Núm. 11, pp. 1875-1882
2018
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Interstitial lung disease in systemic sclerosis: data from the spanish scleroderma study group
Rheumatology International, Vol. 38, Núm. 3, pp. 363-374
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Successful Optimization of Adalimumab Therapy in Refractory Uveitis Due to Behçet's Disease
Ophthalmology, Vol. 125, Núm. 9, pp. 1444-1451
2017
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Clinical and epidemiological differences between men and women with systemic sclerosis: A study in a Spanish systemic sclerosis cohort and literature review
Clinical and Experimental Rheumatology, Vol. 35, pp. S89-S97
2016
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Digital ulcers and cutaneous subsets of systemic sclerosis: Clinical, immunological, nailfold capillaroscopy, and survival differences in the Spanish RESCLE Registry
Seminars in Arthritis and Rheumatism, Vol. 46, Núm. 2, pp. 200-208
2015
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Confirmation of CCR6 as a risk factor for anti-topoisomerase I antibodies in systemic sclerosis
Clinical and Experimental Rheumatology, Vol. 33, pp. 31-35
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Somatic NLRP3 mosaicism in Muckle-Wells syndrome. A genetic mechanism shared by different phenotypes of cryopyrin-associated periodic syndromes
Annals of the Rheumatic Diseases, Vol. 74, Núm. 3, pp. 603-610
2012
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Adalimumab for the treatment of behçet's disease: Experience in 19 patients
Rheumatology (United Kingdom), Vol. 51, Núm. 10, pp. 1825-1831
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Influence of the IL6 gene in susceptibility to systemic sclerosis
Journal of Rheumatology, Vol. 39, Núm. 12, pp. 2294-2302
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Registry of the Spanish Network for Systemic Sclerosis: Clinical Pattern According to Cutaneous Subsets and Immunological Status
Seminars in Arthritis and Rheumatism, Vol. 41, Núm. 6, pp. 789-800
2004
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Intolerancia a la hidroxicloroquina comercializada en España (Dolquine®) en pacientes con patología autoinmune
Revista Clinica Espanola, Vol. 204, Núm. 11, pp. 588-591
1999
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Association of antiphospholipid antibodies with retinal vascular disease in systemic lupus erythematosus
Seminars in Arthritis and Rheumatism, Vol. 28, Núm. 5, pp. 326-332
1998
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Fulminant thrombotic thrombocytopenic purpura in systemic lupus erythematosus
Scandinavian Journal of Rheumatology, Vol. 27, Núm. 1, pp. 76-77
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Trombosis venosa cerebral en la enfermedad de Behcet: Aparicion a pesar del tratamiento anticoagulante
Revista Clinica Espanola