Results 111 to 120 of about 27,529 (230)

Case report: VEXAS as an example of autoinflammatory syndrome in pulmonology clinical practice

Frontiers in Medicine
Lung involvement is not widely recognized as a complication of auto-inflammatory diseases. We present a broad approach to diagnose a severe form of autoinflammatory syndrome in an adult male patient.
Ewa Więsik-Szewczyk, Arkadiusz Zegadło, Agnieszka Sobczyńska-Tomaszewska, Marcelina Korzeniowska, Karina Jahnz-Rózyk   +4 more
doaj   +1 more source

Familial Mediterranean Fever; Recent Advances, Future Prospectives

Diagnostics
Familial Mediterranean Fever (FMF) is the prototype and most common autoinflammatory disease that is particularly frequent in populations originating from the Mediterranean basin. It is characterized by episodes of recurrent inflammation lasting 2–3 days.
Micol Romano, David Piskin, Ovgu Kul Cinar, Erdal Sag   +3 more
doaj   +1 more source

Inflammatory osteolysis: A conspiracy against bone [PDF]

, 2017
Abu-Amer, Abu-Amer, Anton, Bardin, Beranger, Chen, Christo, Claro, Cobelli, Coll, Dapunt, Deborah V. Novack, Dewhirst, Gabriel Mbalaviele, Georg Schett, Gravallese, Harre, Josse, Jovanovic, Kollias, Lukens, Maitra, McCall, Mukai, Negishi-Koga, Osta, Ozen, Pasco, Robaszkiewicz, Rubbert-Roth, Sanchez, Scianaro, Sharma, Steven L. Teitelbaum, Van Hauwermeiren, Wang, Zaki   +36 more
core   +2 more sources

Editorial: Case reports in dermatology

Frontiers in Medicine, 2023
Andreas Recke, Takashi Hashimoto
doaj   +1 more source

Editorial: The role of neutrophils and its NETosis in autoimmunity and autoinflammation

Frontiers in Immunology, 2022
François Niyonsaba, François Niyonsaba
doaj   +1 more source

Case Report: two cases of idiopathic plasmacytic lymphadenopathy subtype of idiopathic multicentric Castleman disease with xanthelasma palpebrum from a Canadian center

Frontiers in Hematology
BackgroundIdiopathic plasmacytic lymphadenopathy is a newly recognized subtype of idiopathic multicentric Castleman disease (iMCD-IPL) and often mimics IgG4-related disease (IgG4-RD).
Andrew A. Y. Chen, Vivian T. Yin, Paula Blanco, Mark Trinder, Richard I. Crawford, Richard I. Crawford, Ryan Henrie, Stephen Parkin, Nasreen Khalil, Mollie Carruthers, Lu Zhang, Luke Y. C. Chen, Luke Y. C. Chen   +12 more
doaj   +1 more source

Exploring targeted therapy in retinal vasculopathy with cerebral leukoencephalopathy: a case report and review of literature

Frontiers in Immunology
Retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations (RVCL-S) is a rare autosomal dominant microvascular disorder caused by C-terminal truncating mutations in TREX1 gene, which impair protein localization and lead to ...
Patricia Tato-Moreno, Patricia Tato-Moreno, Cristina Lavilla Olleros, Cristina Lavilla Olleros, Héctor Balastegui Martín, María Barrientos Guerrero, María Barrientos Guerrero, Anna Mensa-Vilaro, Anna Mensa-Vilaro, María Esther Durán-García, María Esther Durán-García, Paloma Sánchez-Mateos, Paloma Sánchez-Mateos, Elena García-Martínez, Elena García-Martínez   +14 more
doaj   +1 more source

Role of animal models in understanding the mechanisms of autoimmune diseases

Autoimmunity
Autoimmune diseases are diverse, necessitating a mechanistic understanding of the protracted disease process to improve diagnostic accuracy and therapeutic efficacy.
Wasif N. Khan, Grace M. Lacoume, Eric L. Greidinger   +2 more
doaj   +1 more source

How Protein Ubiquitination Can Influence Cytokine Expression—Updated Review on Autoinflammatory VEXAS Syndrome

Immuno
VEXAS syndrome is a new disease entity with symptoms that can mimic hematological, rheumatic and dermatological diseases. It is important to take a multidisciplinary approach to patient care, taking into account genetic testing, in which the presence of ...
Dominika Majer, Matylda Kujawińska, Piotr Limanówka, Łukasz Sędek   +3 more
doaj   +1 more source

Autoinflammatory Disease: Molecular Insights, Clinical Spectrum, and Emerging Therapies

The Journal of Pediatric Academy
Autoinflammatory disease (AID) represents a heterogeneous group of disorders resulting from dysregulation of the innate immune system, independent of autoantibodies or antigen-specific T-cells.
Selen Duygu Arık, Bengisu Menentoğlu, Özlem Akgün   +2 more
doaj   +1 more source