Results 11 to 20 of about 61,143,816 (160)

Tear Lysozyme in Sjögren´s syndrome, Meibomian gland dysfunction, and non-dry-eye. [PDF]

Arq Bras Oftalmol, 2021
Purpose: To evaluate the concentration of tear lysozyme in individuals with Sjogren´s syndrome, meibomian gland dysfunction, and non-dry-eye disease. Methods: Ninety subjects were recruited for this study, including 30 with Sjogren´s syndrome, 30 with ...
Berra M, Galperín G, Berra F, Marquez MI, Mandaradoni M, Tau J, Berra A.   +6 more
europepmc   +2 more sources

Genital Tuberculosis and Serous Cystadenoma in a 58-Year-Old Female With Rheumatoid Arthritis and Sjögren's Syndrome: A Case Report. [PDF]

Case Rep Rheumatol
Genital tuberculosis (GT) is a rare but significant extrapulmonary tuberculosis form, often mimicking ovarian malignancy. We report a case of a 58‐year‐old woman with Sjögren’s syndrome and rheumatoid arthritis, previously treated with infliximab, who presented with abdominal distension, weight loss, night sweats, and intermittent abdominal pain ...
la Cruz-Aragón S, Castillo-Duarte IG, Camacho-Cervantes A, Saad-Ganem A, Rodríguez FMG, Leija-Torres AA.   +5 more
europepmc   +2 more sources

Marcadores inmunológicos como factores pronósticos en el síndrome de Sjögren primario [PDF]

, 2006
[spa] ANTECEDENTES DEL TEMA. El síndrome de Sjögren primario (SSp) es una enfermedad autoinmune sistémica que afecta a las glándulas exocrinas, principalmente las salivales y las lacrimales, originando síntomas de sequedad.
Brito Zerón, María del Pilar
core   +6 more sources

Artificial intelligence processing electronic health records to identify commonalities and comorbidities cluster at Immuno Center Humanitas

Clinical and Translational Allergy, Volume 12, Issue 6, June 2022., 2022
Abstract Background Comorbidities are common in chronic inflammatory conditions, requiring multidisciplinary treatment approach. Understanding the link between a single disease and its comorbidities is important for appropriate treatment and management.
Pierandrea Morandini, Maria Elena Laino, Giovanni Paoletti, Alessandro Carlucci, Tobia Tommasini, Giovanni Angelotti, Jack Pepys, Giorgio Walter Canonica, Enrico Heffler, Victor Savevski, Francesca Puggioni   +10 more
wiley   +1 more source

A importância do diagnóstico e intervenções precoces na síndrome de Sjogren: relato de caso [PDF]

, 2014
A Síndrome de Sjogren é uma doença de progressão lenta, inflamatória, crônica, sistêmica e autoimune que atinge glândulas exócrinas, sobretudo as salivares e as lacrimais. Além disso, pode acometer outros sistemas extraglandulares.
Silva Ramos, Rafaela, Chaveiro Gomes, Fabiana, Menezes de Aquino Ramos, Paula, Rayane Titoto Labre, Sayra, de Melo Prata Mendonça, Fernanda   +4 more
core   +1 more source

STAT4, TRAF3IP2, IL10, and HCP5 Polymorphisms in Sjögren’s Syndrome: Association with Disease Susceptibility and Clinical Aspects

Journal of Immunology Research, Volume 2019, Issue 1, 2019., 2019
Sjögren’s syndrome (SS) is a chronic autoimmune condition characterized by autoantibody production, sicca syndrome, and periepithelial lymphocytic lesions in target tissues. A predisposing genetic background is likely, and, to date, several polymorphisms in non‐HLA genes have been explored with interesting results.
Serena Colafrancesco, Cinzia Ciccacci, Roberta Priori, Andrea Latini, Giovanna Picarelli, Francesca Arienzo, Giuseppe Novelli, Guido Valesini, Carlo Perricone, Paola Borgiani, Senthamil R. Selvan   +10 more
wiley   +1 more source

Nefrocalcinosis y acidosis tubular renal proximal en síndrome de Sjögren

Revista de la Facultad de Ciencias Médicas de Córdoba, 2018
El síndrome de Sjögren primario es una enfermedad autoinmune sistémica de evolución crónica. Puede presentar compromiso renal hasta en un 30% de los pacientes.La incidencia de tubulopatías varía de 2.6 a 33%.
Diego Federico Baenas, Janet Flores Balverdi, Soledad Retamozo, Nadia Riscanevo, Ana Cecilia Álvarez, Verónica Saurit, Jorge De la Fuente, Francisco Caeiro   +7 more
doaj   +1 more source

Abstract

, 2022
Research and Practice in Thrombosis and Haemostasis, Volume 6, Issue S1, October 2022.
wiley   +1 more source

Síndrome Pellizaeus-Merzbacher, Sjogren-Larsson [PDF]

, 1993
Se presenta un extraño caso de Síndrome de Pellizaeus Merzbacher, asociado a un Síndrome de Sjogren-Larsson en una niña ciega puertorriqueña de 16 años con retraso mental y parálisis espástica. La asociación entre ambos síndromes es genética, debido a la
Corpas Pastor, Luis, Machuca Portillo, María del Carmen   +1 more
core   +1 more source

Abstract Book for the 27th Congress of the European Hematology Association

, 2022
HemaSphere, Volume 6, Issue S3, Page 1-4130, June 2022.
wiley   +1 more source