Results 11 to 20 of about 58,978,997 (155)
Enfermedad de Behçet asociada a trombosis venosa [PDF]
Revista de la Asociación Colombiana de Dermatología y Cirugía Dermatológica, 2019 La enfermedad de Behçet es una enfermedad crónica y multisistémica, caracterizada por uveítis, úlceras orales y úlceras genitales recurrentes. Se reporta un paciente con enfermedad de Behçet asociada a trombosis venosa profunda, que presentó edema en la
Yury Alexander Usuga +3 more
doaj +1 more source
Enfermedad de Behçet: Reporte de 5 casos
Revista Reumatología al Día, 2022 La enfermedad de Behçet (EB) es una vasculitis sistémica de causa desconocida.1 En el Ecuador no hay estudios epidemiológicos de la enfermedad y de su diversidad clínica, por lo que se realizó la revisión de 5 pacientes ambulatorios con EB, basados en ...
Patricia Arteaga +3 more
doaj +1 more source
Enfermedad de Behçet: Reporte de un caso clínico pediátrico
Revista Reumatología al Día, 2019 La enfermedad de Behçet es una vasculitis de etiología desconocida, frecuente en los países de oriente, caracterizada por úlceras orales, genitales, uveítis y manifestaciones cutáneas.
Cristina Herrera
doaj +1 more source
Úlceras orales a repetición y eritema nodoso: pensar en Enfermedad de Behçet [PDF]
Revista Methodo, 2018 La enfermedad de Behçet es una vasculitis sistémica crónica recurrente poco habitual en nuestro país. Se caracteriza por afectación mucocutánea, pero también, compromete otros órganos como ojo, sistema nervioso, gastrointestinal, musculoesquelético ...
Gutiérrez Magaldi I +6 more
doaj +1 more source
Síndrome de Adamantiades-Behçet. Informe de un caso [PDF]
, 2021 Adamantiades-Behcet Syndrome is a multsystemicinflammatory disease which is most common in Oriental Mediterranean basin, Asia and Turkey. A case report is presented related to a 52 year-old male patient who showed oral ulcers, uveitis, euphoria and ...
Palmero Marrero, Roxana +1 more
core +1 more source
PROTEOMICS, Volume 21, Issue 23-24, December 2021., 2021 Abstract T cells play an important role in the adaptive immune response to a variety of infections and cancers. Initiation of a T cell mediated immune response requires antigen recognition in a process termed MHC (major histocompatibility complex) restri ction.
Sebastian Joyce, Nicola Ternette
wiley +1 more source
Glucocorticoid‐induced osteonecrosis in systemic lupus erythematosus patients
Clinical and Translational Medicine, Volume 11, Issue 10, October 2021., 2021 ON is a complex and multifactorial complication of Systemic Lupus Erythematosus (SLE). However, the pathophysiology and risk factors for ON in patients with SLE have not been fully determined yet. Here, we review the epidemiology, risk factors, diagnosis, and treatment options for glucocorticoid‐induced ON, with a specific focus on patients with SLE ...
Kaichi Kaneko +5 more
wiley +1 more source
Manifestaciones gastrointestinales de la enfermedad de Behçet
, 2022 Behçet\u27s Disease (BD) is a rare, idiopathic, chronic and relapsing entity; characterized by multisystem involvement. The gastrointestinal tract has aroused special interest, as it is associated with higher morbidity and mortality and given its ...
Rojas-Zuleta, Wilmer Gerardo +3 more
core +2 more sources
British Journal of Haematology, Volume 194, Issue 1, Page 195-199, July 2021., 2021 Summary Autoimmune disease is a risk factor for first incident venous thromboembolism (VTE). However, data on the risk of recurrent VTE in people with autoimmune disease is sparse. We explored the risk of recurrent VTE using the RIETE registry, comparing people with autoimmune disease (n = 1305) to those without (n = 50608).
Jaime Borjas Howard +10 more
wiley +1 more source
Neuro-Behçet: diagnóstico diferencial de enfermedades desmielinizantes [PDF]
, 2022 The Behçet´s disease (BD) is an inflammatory multisystemic vasculitis of unknown etiology and is classified as a rare disease in the USA and European countries.
Rivera Sandoval, Natalia +3 more
core +2 more sources