Results 31 to 40 of about 27,299 (305)
Audio-vestibular symptoms in systemic autoimmune diseases [PDF]
, 2018 Immune-mediated inner ear disease can be primary, when the autoimmune response is against the inner ear, or secondary. The latter is characterized by the involvement of the ear in the presence of systemic autoimmune conditions. Sensorineural hearing loss
Adelchi, Croce +7 more
core +1 more source
Classic polyarteritis nodosa associated with hepatitis C virus infection: a case report
Journal of Medical Case Reports, 2012 Introduction Hepatitis C virus has been under-recognized as an etiologic factor for polyarteritis nodosa and the presence of hepatitis C antigenemia in patients with polyarteritis nodosa has been reported as insignificant.
Rodrigo Damith +2 more
doaj +1 more source
CUTANEOUS POLYARTERITIS NODOSA: A REPORT OF TWO CASES [PDF]
Acta Medica Iranica, 1998 Polyarteritis nodosa is a multisystem necrotizing vasculitis of small and medium size muscular arteries in which involvement of the renal and viserat arteries is characteristic.
Z . Nowroozi
doaj +1 more source
Turkish Journal of Internal Medicine, 2021 Aortic diseases have high mortality and are usually late or misdiagnosed. Especially in patients with inflammatory vasculitis, diagnosis is often confused with other causes of chest pain and this causes a delay in diagnosis.
Hatice Taşkan +4 more
doaj +1 more source
Uveitis, 2020 The first description of polyarteritis nodosa (PAN) was in 1852 by Karl Rokitansky, a Pathologist at the University of Vienna.(1) The initial report describes a 23 year-old man who had a five-day history of fever and diarrhea.
Jordan A. Ueberroth
semanticscholar +1 more source
Annals of the Rheumatic Diseases, 2020 We read the paper by Rimar et al 1 in your journal with great interest. They reported the case with refractory polyarteritis nodosa treated with tofacitinib, a janus kinase inhibitor, successfully.
M. Akiyama, Y. Kaneko, T. Takeuchi
semanticscholar +1 more source
Muscular Polyarteritis Nodosa: A Case Series Study of 6 Patients
Annals of Internal Medicine: Clinical Cases, 2022 A subset of polyarteritis nodosa known as muscular polyarteritis nodosa (MPAN) is a disease process that remains mostly limited to the muscle. Here, we report 6 patient cases of MPAN for which we investigated the clinical features. We examined 6 patients
Fumitoshi Fukuzawa +7 more
doaj +1 more source
Systemic lupus erythematosus and hearing disorders: literature review and meta-analysis of clinical and temporal bone findings [PDF]
, 2017 Objective: This literature review and meta-analysis was performed to evaluate the correlations among hearing and vestibular clinical symptoms, temporal bone findings, and pathological mechanisms in patients with systemic lupus erythematosus (SLE).
DI STADIO, Arianna, Ralli, Massimo
core +1 more source
Genetic flow directionality and geographical segregation in a Cymodocea nodosa genetic diversity network [PDF]
EPJ Data Science, 1:11, 2012, 2012 We analyse a large data set of genetic markers obtained from populations of Cymodocea nodosa, a marine plant occurring from the East Mediterranean to the Iberian-African coasts in the Atlantic Ocean. We fully develop and test a recently introduced methodology to infer the directionality of gene flow based on the concept of geographical segregation ...
arxiv +1 more source
Arterial distensibility in children and teenagers: Normal evolution and the effect of childhood vasculitis [PDF]
, 2002 Background: Polyarteritis nodosa is a necrotising vasculitis of the medium sized and small muscular arteries. The inflammatory and subsequent reparative processes may alter the arterial mechanical properties.
Brogan, PA +4 more
core +2 more sources