Results 141 to 150 of about 273,619 (385)

Updates in ANCA-associated vasculitis

European Journal of Rheumatology, 2022
Carolyn Ross, Jean-Paul Makhzoum, Christian Pagnoux   +2 more
doaj   +1 more source

THE ROLE OF POLYMORPHONUCLEAR LEUKOCYTES IN THE INITIATION AND CESSATION OF THE ARTHUS VASCULITIS [PDF]

, 1959
Charles G. Cochrane, William O. Weigle, Frank J. Dixon   +2 more
openalex   +1 more source

Efficacy and Safety of Belimumab and Azathioprine for Maintenance of Remission in Antineutrophil Cytoplasmic Antibody–Associated Vasculitis: A Randomized Controlled Study

Arthritis & Rheumatology, 2019
To evaluate the safety and efficacy of belimumab as adjunctive therapy to maintain remission in antineutrophil cytoplasmic antibody (ANCA)–associated vasculitis (AAV).
D. Jayne, D. Blockmans, R. Luqmani, S. Moiseev, B. Ji, Y. Green, L. Hall, D. Roth, R. B. Henderson, P. Merkel   +9 more
semanticscholar   +1 more source

Takayasu's arteritis in an adult female from Cameroon: diagnosis via Doppler echocardiography [PDF]

, 2016
No abstract ...
Aminde, Leopold N, Dzudie, Anastase, Njim, Tsi, Noubiap, Jean Jacques N., Takah, Noah   +4 more
core   +1 more source

Porto‐sinusoidal vascular disorder in a pediatric patient with prolidase deficiency: A case report

JPGN Reports, EarlyView.
Abstract Prolidase deficiency (PD) is a rare autosomal recessive disorder affecting collagen turnover, leading to diverse clinical manifestations including dermatologic lesions, hepatosplenomegaly, and vascular anomalies. Liver involvement in PD is poorly understood, with few reported cases.
Melissa Castro, Christian Martinez, Carole Brathwaite, Reuven Bromberg, Ana M. Rodriguez, Erick Hernandez   +5 more
wiley   +1 more source

Persistent B Cell Depletion After Rituximab for Autoimmune and Glomerular Diseases: A Case Series

Kidney International Reports
Introduction: Persistent B cell depletion is a rare complication of rituximab treatment, and its clinical implications are unknown. Methods: This retrospective case series included patients with glomerular and autoimmune diseases who developed persistent
Orhan Efe, Gabriel Sauvage, Anushya Jeyabalan, Ayman Al Jurdi, Harish S. Seethapathy, Katherine Cosgrove, Frank B. Cortazar, Karen A. Laliberte, Reza Zonozi, John L. Niles   +9 more
doaj  

Hypocomplementemic urticarial vasculitis complicated with diffuse alveolar hemorrhage: a case report and review of literature

Italian Journal of Medicine, 2014
Urticarial vasculitis is a small-vessel vasculitis characterized clinically by urticaria and microscopically by leukocytoclastic vasculitis. Hypocomplementemic urticarial vasculitis syndrome is a rare subtype of urticarial vasculitis with organ ...
Paola Gnerre, Sandra Buscaglia, Alessandro Cattana, Andrea Pestarino, Silvia Ardoino, Ezio Venturino, Lionello Parodi   +6 more
doaj   +1 more source

Pseudomonas Infections in Mink with Special Reference to Pseudomonas Vasculitis in Pulmonary Lesions [PDF]

, 1968
Knut Nordstoga
openalex   +1 more source

Vasculitis: an update

British Journal of Hospital Medicine, 2014
The systemic vasculitides are uncommon but serious diseases. Early recognition can be difficult because they mimic many conditions. Aggressive immunosuppression is toxic but effective; a targeted approach with biological agents may improve the outcome.
openaire   +4 more sources

Head and Neck Manifestations of Eosinophilic Granulomatosis with Polyangiitis: A Systematic Review. [PDF]

, 2016
OBJECTIVE: To conduct the first and only systematic review of the existing literature on head and neck manifestations of eosinophilic granulomatosis with polyangiitis to guide clinical decision making for the otolaryngologist.
Basnyat, Shristi, Goldfarb, Jared M., Nyquist, Gurston G., Rabinowitz, Mindy R., Rosen, Marc R.   +4 more
core   +1 more source