Results 101 to 110 of about 51,881 (280)

Granulomatous hepatitis caused by Q fever: a differential diagnosis of fever of unknown origin

open access: yesAnnals of Hepatology, 2013
The differential diagnosis of fever of unknown origin (FUO) includes infectious, neoplastic, rheumatic-inflammatory and miscellaneous diseases. We report the case of a 35-year-old man with FUO caused by Q fever.
Nancy Aguilar-Olivos   +5 more
doaj   +1 more source

ANTICARDIOLIPIN ANTIBODIES IN ACUTE RHEUMATIC-FEVER

open access: yes, 1992
Recent reports describe the association of antiphospholipid antibodies (aPL) with chorea or severe heart valve lesions in systemic lupus erythematosus, lupus-like disease, or the primary antiphospholipid antibody syndrome.
RIEDEL, I   +6 more
core  

Asthma and Multimorbidity Amongst Ethnic Minority Groups in High Income Countries

open access: yesClinical &Experimental Allergy, EarlyView.
There is a tight intersection between asthma, deprivation, ethnicity, multimorbidity and poor clinical outcomes. An integrated, holistic and culturally tailored approach is needed to improve clinical outcomes amongst ethnic minority groups with asthma and multimorbidity. ABSTRACT Asthma is one of the commonest noncommunicable diseases worldwide.
Mamidipudi Thirumala Krishna   +6 more
wiley   +1 more source

Acute non-rheumatic myocarditis following group G streptococcal pharyngitis: a rare mimic of acute myocardial ischemia in a young adult

open access: yesEuropean Journal of Case Reports in Internal Medicine
Background: Acute myocarditis is a rare but serious inflammatory condition of the myocardium, often triggered by infections or rheumatic heart disease. While group A Streptococcus is commonly associated with bacterial myocarditis, group G Streptococcus ...
Elizabeth R. Rimsky   +5 more
doaj   +1 more source

S1 Guideline: Therapy of generalized pustular psoriasis

open access: yesJDDG: Journal der Deutschen Dermatologischen Gesellschaft, EarlyView.
Summary The S1 guideline “Therapy of generalized pustular psoriasis (GPP)” is a German guideline developed in accordance with the criteria of the AWMF. The full version addresses clinical presentation, pathogenesis, diagnosis and differential diagnosis, comorbidities, and therapy.
Rotraut Mößner   +17 more
wiley   +1 more source

Rhythm and Conduction Analysis of Patients With Acute Rheumatic Fever

open access: yes, 2013
Various rhythm and conduction abnormalities can develop in acute rheumatic fever. This study investigated rhythm and conduction abnormalities in children with acute rheumatic fever using a standard 12-lead electrocardiogram and 24-h rhythm Holter ...
Ece, Ibrahim   +3 more
core   +1 more source

An unusual presentation of osteochondrosis in the elbows and tarsi of a Friesian colt

open access: yesEquine Veterinary Education, EarlyView.
Summary This case report describes the clinical, diagnostic imaging results and post‐mortem findings in a foal that underwent reassessment following surgical management of angular limb deformities (ALD) and acute onset of gait abnormalities. Upon presentation, the foal showed an abnormal stiff gait characterised by bilateral medial limb collapse during
A. Torrent‐Crosa   +3 more
wiley   +1 more source

Clinical Characteristics of Patients with Acute Rheumatic Fever and Rheumatic Heart Disease in Kosovo, Evaluation of the Long-Term Results

open access: yes, 2016
Background. Rheumatic fever, also known as acute rheumatic fever (ARF), is an inflammatory disease that can involve the heart, joints, skin, and brain.[1] The disease typically develops two to four weeks after a throat infection.[2] Signs and symptoms ...
Berisha, Idriz   +5 more
core   +1 more source

acute rheumatic fever patient

open access: yes
Acute Rheumatic Fever- young boy laying down in his ...

core  

Australian clinical practice guideline: diagnosis and treatment of idiopathic multicentric Castleman disease

open access: yesInternal Medicine Journal, EarlyView.
Abstract Idiopathic multicentric Castleman disease (iMCD) is a rare condition. The pathogenesis is incompletely understood; however, interleukin‐6 (IL‐6) is a major mediator. The clinical presentation is heterogeneous, from mild constitutional symptoms to severe multi‐organ failure.
Dipti Talaulikar   +16 more
wiley   +1 more source

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