Results 41 to 50 of about 14,024 (212)
Polyarteritis Nodosa – eine verschwindende Erkrankung dank Identifikation der Hauptursache [PDF]
The polyarteritis nodosa is a vasculitis for which the main cause had been identified as hepatitis B, a chronic infectious disease inducing an overshooting immune reaction.
Frey, Felix Julius
core
HYPERTROPHIC CARDIOMYOPATHY ASSOCIATED WITH POLYARTERITIS NODOSA: A CASE OF SUDDEN CARDIAC DEATH
This case concerns a rare sudden cardiac death characterized by macroscopic and microscopic post-mortem findings of hypertrophic cardiomyopathy and polyarteritis nodosa.
Elvira Ventura Spagnolo
doaj +1 more source
Updated COVID‐19 Vaccines and Health Outcomes in Patients With Autoimmune Rheumatic Conditions
Objective We aimed to assess the association between COVID‐19 vaccination status and COVID‐19‐related hospital admissions, need for mechanical ventilation or extracorporeal membrane oxygenation (ECMO), and death in people with autoimmune rheumatic conditions. Methods We conducted a retrospective cohort study using National Clinical Cohort Collaborative
Lesley E. Jackson +127 more
wiley +1 more source
Rare vasculitis types and obstetric and neonatal outcomes – A population‐based study
Abstract Objective Vasculitis is an infrequent pathology among reproductive‐aged women. While data exists regarding pregnancy outcomes in the more common vasculitis subtypes, data is limited regarding these outcomes in rare vasculitis subtypes. We aimed to compare pregnancy and perinatal outcomes between women who suffered from rare types of vasculitis
Uri Amikam +4 more
wiley +1 more source
Poliarteritis nodosa cutánea [PDF]
Classic systemic polyarteritis nodosa (PAN) is a necrotizing vasculitis of smalland medium-sized arteries. On the other hand, cutaneous polyarteritis nodosa is designated for the cutaneous limited form (deep dermis and panniculus) of PAN.  ...
Cárdenas, Luis Fernando
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ABSTRACT Introduction/Aims Electrophysiologic features suggestive of demyelination have been reported in vasculitic neuropathy, complicating the diagnostic process, but their frequency is unknown. We aimed to determine the prevalence of demyelinating features, including fulfillment of European Academy of Neurology/Peripheral Nerve Society (EAN/PNS ...
Alexandra Maury +7 more
wiley +1 more source
Multiple intrahepatic arterial aneurysms and spontaneous aneurysmal rupture associated with polyarteritis nodosa leading to hemoperitoneum are extremely rare occurrences, but the conditions can be life-threatening if left untreated because of the risk of
Myung Jin Seol +3 more
doaj +1 more source
Inborn errors of immunity in children with neuroinflammation
Abstract Inborn errors of immunity (IEIs), an expanding group of monogenic disorders with diverse clinical manifestations, are increasingly recognized to include neuroinflammatory disease. Examples of diseases included under this umbrella are Aicardi–Goutières syndrome, deficiency of adenosine deaminase 2, familial haemophagocytic lymphohistiocytosis ...
Eppie M Yiu +5 more
wiley +1 more source
POLYARTERITIS NODOSA WITH NEW BONE FORMATION
1. A case of polyarteritis nodosa is reported, the presenting manifestation of which was subperiosteal new bone formation in both legs. 2. The effect of cortisone on the symptoms is recorded. 3.
Paul D. Saville
core +1 more source
The aim of the study – to determine the diagnostic value of serum levels of endothelin-1, alpha-actin-2 and elastin in patients with primary systemic vasculitis. Materials and methods.
L. B. Petelytska, O. B. Yaremenko
doaj +1 more source

