Results 211 to 220 of about 1,195,397 (240)
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American Journal of Critical Care, 2010
Scenario:A 59-year-old woman had brief episodes of rapid atrial fibrillation and bradycardia several months ago. It was not recurrent or sustained, so she was not treated with invasive or pharmacological interventions but followed up with occasional clinic visits.
Michele M, Pelter, Mary G, Carey
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Scenario:A 59-year-old woman had brief episodes of rapid atrial fibrillation and bradycardia several months ago. It was not recurrent or sustained, so she was not treated with invasive or pharmacological interventions but followed up with occasional clinic visits.
Michele M, Pelter, Mary G, Carey
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Behçet’s disease as a systemic disease
Clinics in Dermatology, 2014Behçet's disease usually begins with cutaneous manifestations, such as recurrent aphthous stomatitis, genital ulcers, erythema nodosum-like lesions, papulopustular findings, and pathergy phenomenon. Recurrent aphthous stomatitis is generally the first sign, and other findings may develop in the course of the disease.
M Cem, Mat +3 more
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Systemic Erdheim–Chester disease
Virchows Archiv, 2008Erdheim-Chester disease is a rare xanthomatosis that may present with characteristic radiologic and histologic features. There have been conflicting reports regarding the nature of this process, including whether it represents a reactive or neoplastic lesion. We present the clinical histories, pathologic findings, and an analysis of clonality using the
Brendan Craig, Dickson +8 more
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Annals of Internal Medicine, 1963
Excerpt Urticaria pigmentosa was first described in 1869 by Nettleship (1) and named by Sangster (2) in 1878. In this disease, mast cell infiltration is confined entirely to the skin.
R D, MUTTER, M, TANNENBAUM, J E, ULTMANN
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Excerpt Urticaria pigmentosa was first described in 1869 by Nettleship (1) and named by Sangster (2) in 1878. In this disease, mast cell infiltration is confined entirely to the skin.
R D, MUTTER, M, TANNENBAUM, J E, ULTMANN
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ains · Anästhesiologie · Intensivmedizin · Notfallmedizin · Schmerztherapie, 2003
F, Hrska, W, Graninger, M, Frass
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F, Hrska, W, Graninger, M, Frass
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Systemic Weber-Christian Disease
Journal of Cutaneous Medicine and Surgery, 2000Background: Weber-Christian disease is a controversial entity that histologically presents as a lobular panniculitis. A systemic variant of this disorder, in which visceral fat is affected, has been reported. Objective: A 29-year-old woman with Weber-Christian disease developed a rapidly enlarging abdominal mass during hospitalization for a flare of ...
M A, Ter Poorten , B H, Thiers
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Menstruation and Systemic Disease
New England Journal of Medicine, 1958Diabetes Mellitus It is said that adult diabetes commonly results in infrequent and scanty uterine bleeding, amenorrhea, decreased libido and sterility.248 In children with poorly controlled diabet...
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Postgraduate Medicine, 1971
As a first step in analyzing dementia in a patient with or without signs of systemic disease, the mental deterioration needs to be defined. The effects of the dementia on different components of memory are clues to the location of processes causing memory loss.
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As a first step in analyzing dementia in a patient with or without signs of systemic disease, the mental deterioration needs to be defined. The effects of the dementia on different components of memory are clues to the location of processes causing memory loss.
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2012
VasculitisThe classification of paediatric vasculitis 168The epidemiology of paediatric vasculitis 171The investigation of primary systemic vasculitis 172The standard treatment of childhood vasculitis 174Henoch–Schönlein purpura 179Kawasaki disease 183The anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides ...
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VasculitisThe classification of paediatric vasculitis 168The epidemiology of paediatric vasculitis 171The investigation of primary systemic vasculitis 172The standard treatment of childhood vasculitis 174Henoch–Schönlein purpura 179Kawasaki disease 183The anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitides ...
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2018
This chapter covers the full spectrum of systemic diseases in paediatric rheumatology including: the systemic vasculitides (HSP, Kawasaki disease, PAN, ANCA-associated vasculitis, Takayasu arteritis, Behçet's disease, cerebral vasculitis, and many others); juvenile SLE; scleroderma; JDM; overlap syndromes; antiphospholipid syndrome; sarcoid; and ...
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This chapter covers the full spectrum of systemic diseases in paediatric rheumatology including: the systemic vasculitides (HSP, Kawasaki disease, PAN, ANCA-associated vasculitis, Takayasu arteritis, Behçet's disease, cerebral vasculitis, and many others); juvenile SLE; scleroderma; JDM; overlap syndromes; antiphospholipid syndrome; sarcoid; and ...
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