Zobrazeno 1 - 10
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pro vyhledávání: '"J. Álvarez-Troncoso"'
Akademický článek
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Akademický článek
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Publikováno v:
Medicine - Programa de Formación Médica Continuada Acreditado. 13:1985-1994
espanolLas vasculitis de gran vaso afectan predominantemente a la arteria aorta y sus ramas y se clasifican en dos entidades principales: la arteritis de celulas gigantes (ACG) y la arteritis de Takayasu (ATK). La ACG suele presentarse con cefalea te
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ab77db9cc9fac96f60e36e404d8ac182
https://doi.org/10.1016/j.med.2021.05.011
https://doi.org/10.1016/j.med.2021.05.011
Autor:
J. Álvarez Troncoso, Á. Robles Marhuenda, R. Sorriguieta Torre, S. Carrasco Molina, C. Soto Abánades, A. Noblejas Mozo, E. Martínez Robles, C. Sánchez Díaz, J. J. Rios
Publikováno v:
Annals of the Rheumatic Diseases. 81:1371.2-1372
BackgroundSLICC Damage Index (SDI) index was designed to reflect accrual damage in patients with systemic lupus erythematosus (SLE). It reflects an irreversible change, unrelated to inflammatory activity, that has occurred since the diagnosis of SLE,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f982558f9026df981ae422a804a3161
https://doi.org/10.1136/annrheumdis-2022-eular.1870
https://doi.org/10.1136/annrheumdis-2022-eular.1870
Akademický článek
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Autor:
E. Ruiz Bravo, F. Arnalich Fernández, C. Soto Abánades, L. Ramos Ruperto, J. J. Rios, C. M. Oñoro López, Á. Robles Marhuenda, L. Blasco Santana, E. Martínez Robles, A. Noblejas Mozo, J. Álvarez Troncoso
Publikováno v:
Annals of the Rheumatic Diseases. 80:1192.1-1192
Background:Sjögren’s syndrome (SS) is a systemic autoimmune disease characterized by mononuclear cell infiltration of the exocrine glands, which leads to sicca syndrome and systemic manifestations. The minor salivary gland biopsy (MSGB) is undoubt
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c4b82350cce838ef7d32561358d812d5
https://doi.org/10.1136/annrheumdis-2021-eular.3251
https://doi.org/10.1136/annrheumdis-2021-eular.3251
Autor:
M. C. Vega Cabrera, J. C. Santacruz Mancheno, A. Díez Vidal, Á. Robles Marhuenda, B. Rivas, S. Afonso Ramos, A. Noblejas Mozo, F. Arnalich Fernández, J. Álvarez Troncoso, J. J. Rios, T. Olea Tejero, C. Soto Abánades, E. Martínez Robles
Publikováno v:
Annals of the Rheumatic Diseases. 80:270.2-271
Background:Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides (AAV) include granulomatosis with polyangiitis (GPA), microscopic polyangiitis (MPA), and eosinophilic granulomatosis with polyangiitis (EPGA). Renal involvement is freque
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6bd89f44ae0a683667da301882ae227
https://doi.org/10.1136/annrheumdis-2021-eular.345
https://doi.org/10.1136/annrheumdis-2021-eular.345
Autor:
Pilar Nozal, J. J. Rios, J. Álvarez Troncoso, F. Arnalich Fernández, E. Martínez Robles, C. Soto Abánades, A. Noblejas Mozo, S. Carrasco Molina, Á. Robles Marhuenda, J. Valdivieso
Publikováno v:
Annals of the Rheumatic Diseases. 80:693.2-694
Background:Myositis-specific antibodies (MSA) are highly specific and useful to classify patients as having syndromes with distinct clinical features and prognosis. MSA are almost always mutually exclusive and quite specific, adding value as a useful
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e03885062a01ca668d0a4253ab3062cf
https://doi.org/10.1136/annrheumdis-2021-eular.3234
https://doi.org/10.1136/annrheumdis-2021-eular.3234
Autor:
L. Blasco Santana, Á. Robles Marhuenda, J. J. Rios, L. Ramos Ruperto, A. Noblejas Mozo, C. M. Oñoro López, J. Álvarez Troncoso, F. Arnalich Fernández, R. Sorriguieta Torre, E. Martínez Robles, E. Ruiz Bravo, C. Soto Abánades
Publikováno v:
Annals of the Rheumatic Diseases. 79:1497.1-1498
Background:Sjögren’s syndrome (SjS) is a systemic autoimmune disease with a broad clinical presentation from dry syndrome to systemic extraglandular manifestations. The diagnosis can be complex since none of the markers, except anti-Ro, is suffici
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30b258db9b0d0d0f8cd85d513fdcc4d3
https://doi.org/10.1136/annrheumdis-2020-eular.4921
https://doi.org/10.1136/annrheumdis-2020-eular.4921
Autor:
L. Ramos Ruperto, J. J. Rios, A. Díez Vidal, J. Álvarez Troncoso, Á. Robles Marhuenda, F. Arnalich Fernández, G. Daroca Bengoa, A. De Gea Grela, C. Soto Abánades, A. Noblejas Mozo, E. Martínez Robles
Publikováno v:
Annals of the Rheumatic Diseases. 79:1041.1-1041
Background:Antiphospholipid syndrome (APS) is a systemic autoimmune disease, associated with a hypercoagulable state and fetal loss and with other clinical manifestations including cardiac involvement. APS occurs as a primary disorder (PAPS) or secon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a66dd2a6307ae1b15ece03468e68bb7
https://doi.org/10.1136/annrheumdis-2020-eular.4958
https://doi.org/10.1136/annrheumdis-2020-eular.4958