Results 21 to 30 of about 16,344 (265)
Elicitation of expert prior opinion:application to the MYPAN trial in childhood polyarteritis nodosa [PDF]
, 2015 Objectives Definitive sample sizes for clinical trials in rare diseases are usually infeasible. Bayesian methodology can be used to maximise what is learnt from clinical trials in these circumstances.
, MYPAN Vasculitis Expert Group +15 more
core +1 more source
Familial polyarteritis nodosa [PDF]
Arthritis & Rheumatism, 1994 AbstractFamilial polyarteritis nodosa (PAN) is rare. We describe here two siblings who developed PAN 8 years apart. HLA typing showed that the affected family members shared a common haplotype with their unaffected mother. Further study of the family history suggested the possibility of an inherited disorder of connective tissue predisposing to ...
J C, Mason +8 more
openaire +2 more sources
Medicine Science, 2014 Polyarteritis nodosa is multisystem disease with necrotizing vasculitis of middle and small sized arteries. Takayasu arteritis is a rare nonspecific inflammatory disease with unknown cause, predominantly affecting the aorta and its main branches.
Onur Gurer, Ismail Haberal
doaj +1 more source
A rare case of Polyarteritis Nodosa associated with autoimmune hepatitis: a case report
BMC Rheumatology, 2021 Background Polyarteritis nodosa is a type of vasculitis affecting medium- and small-sized arteries that has been associated with hepatitis B but does not have an established relationship with autoimmune hepatitis.
Freda Kennedy +5 more
doaj +1 more source
Case Reports in Pediatrics, 2016 Pediatric polyarteritis nodosa is rare systemic necrotizing arteritis involving small- and medium-sized muscular arteries characterized by aneurysmal dilatations involving the vessel wall.
Kae Watanabe +2 more
doaj +1 more source
Necrosis of the small intestine leading to a diagnosis of polyarteritis nodosa: a case report
Journal of Medical Case Reports, 2019 Background Polyarteritis nodosa is a disease that presents with necrotizing vasculitis in small and medium-sized arteries. It may occur in various organs, but approximately half of cases have gastrointestinal involvement.
Saori Yajima +6 more
doaj +1 more source
Spontaneous kidney rupture in polyarteritis nodosa presenting as an acute abdomen [PDF]
, 1991 CITATION: Edelstein, C. L. & Welke, H. 1991. Spontaneous kidney rupture in polyarteritis nodosa presenting as an acute abdome. South African Medical Journal, 79:52-53.The original publication is available at http://www.samj.org.zaAn acute abdomen in a ...
Edelstein, C. L., Welke, H.
core +1 more source
Journal of Medical Case Reports, 2019 Background Polyarteritis nodosa is a small vessel to medium vessel vasculitis that frequently presents with multi-organ involvement, but can sometimes be limited to single organs such as the testes.
Mohan Stewart +3 more
doaj +1 more source
Therapeutic advances in the treatment of vasculitis [PDF]
, 2016 Considerable therapeutic advances for the treatment of vasculitis of the young have been made in the past 10 years, including the development of outcome measures that facilitate clinical trial design.
Brogan, PA, Eleftheriou, D
core +2 more sources
Rituximab Efficacy during a Refractory Polyarteritis Nodosa Flare
Case Reports in Medicine, 2009 Polyarteritis nodosa (PAN) is a systemic vasculitis whose severe forms are treated with glucocorticoids and cyclophosphamide. Refractory patients are exposed to many complications, notably accelerated atherosclerosis.
Emmanuel Ribeiro +7 more
doaj +1 more source