Results 101 to 110 of about 5,850 (214)

Wegener`s granulomatosis and mucoromycosis: A case study and review of literature

open access: yesAdvanced Biomedical Research, 2012
Mucormycosis is a fatal invasive infection which mostly involves diabetic or immunosuppressed patients. Early diagnosis, improving immunosuppression, systemic antifungal therapy, and surgical debridement are necessary for successful treatment.
Sayyed Mojtaba Abtahi   +5 more
doaj   +1 more source

Primary Systemic Vasculitis in Childhood [PDF]

open access: yes, 2012
As vasculites sistémicas constituem um grupo de doenças, pouco frequentes na infância, caracterizadas por inflamação e necrose vascular. A sua tradução clínica é heterogénea, condicionada pelo tipo de vaso e orgão afectados. Recentemente foi proposta uma
Amaro, C, Pereira, N
core  

Autoanticuerpos y vasculitis sistémicas

open access: yesRevista de la Facultad de Ciencias Médicas de Córdoba, 2010
El término vasculitis incluye un grupo heterogéneo de enfermedades que tienen en común la lesión inflamatoria de los vasos sanguíneos. La evolución de este proceso inflamatorio conduce a la isquemia o, en ocasiones, hemorragia de los órganos dependientes
Paula Alba   +2 more
doaj   +1 more source

Queilitis granulomatosa de Miescher [PDF]

open access: yes, 2017
La queilitis granulomatosa es un raro proceso de etiología desconocida que se considera una forma oligosintomática del síndrome de Melkersson-Rosenthal.
Alsina Gibert, Mercè   +2 more
core  

Limited wegener′s granulomatosis presenting as multiple retinal vascular occlusions

open access: yesIndian Journal of Ophthalmology, 2002
In the early stages of Wegener′s granulomatosis, and in the atypical forms, the classic clinicopathologic features of the disease are often absent, delaying diagnosis.
Shenoy Radha   +3 more
doaj  

Granulomatosis with polyangiitis in children: report of a case with kidney-lung syndrome = Granulomatosis con poliangitis en pediatría: a propósito de un caso con síndrome pulmón-riñón

open access: yesIatreia, 2013
Granulomatosis with polyangiitis as a cause of kidney-lung syndrome is uncommon in children. We report the case of a 13 year old patient with alveolar hemorrhage, rapidly progressive glomerulonephritis, episcleritis and anti PR3.
Muñoz Grajales, Carolina   +2 more
doaj  

Characteristics of articular syndrome in systemic vasculitis [PDF]

open access: yes, 2017
The purpose of the study – investigation the separate joint lesion in systemic vasculitis, their X-ray sonographic characteristics, the correlation of the articular syndrome severity with extra-articular manifestations of the diseases, as well as ...
Gashynova, K.   +4 more
core  

Lymphocyte counts in patients with ANCA-associated vasculitis [PDF]

open access: yes, 2018
How lymphocyte counts relate to treatment-response in patients with ANCA-associated vasculitis (AAV) is controversial, and data on short-term variability of lymphocyte counts are lacking.
Berger, Christoph   +4 more
core  

بازسازی کامل بینی پس از تخریب به علت گرانولوماتوز وگنر [PDF]

open access: yes, 2014
تغییر شکل بینی یکی از عوارض ضایع در گرانولوماتوز وگنر است که علت آن درگیری عروق سایز متوسط می¬باشد. این بیماری می¬تواند منجر به نکروز و تخریب مخاط بینی و اسکلت استخوانی غضروفی شود.
حافظی, فرهاد   +4 more
core  

The Role of Environmental Factors in the Pathogenesis of Anti-Neutrophil Antibody Associated Vasculitis

open access: yes, 2014
This review seeks to critically examine the environmental factors reported to be associated with anti-neutrophil antibody associated systemic vasculitis. The published literature was searched in a systematic fashion.
Gatenby, Paul A
core   +1 more source

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