PURPURIC FEVER.

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منابع مشابه

Potential virulence-associated factors in Brazilian purpuric fever. Brazilian Purpuric Fever Study Group.

Centers for Disease Control, Atlanta, Georgia 30333'; Division of Infectious Diseases, Departinent of Internul Medicine, The University of Texas Health Sciences Center, Dallas, Texas 75206-; Depautnent of Microbiologv, Georgetown Uni'ersitv, Washington, D.C. 200573; Depautrnent of Microbiology and Public Health, Michigan State University, East Lansing, Michigan 488244, Departinent of Pathologv ...

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Epidemiology and clinical spectrum of Brazilian purpuric fever. Brazilian Purpuric Fever Study Group.

Meningitis and Special Pathogens Braunch, Division ofBacterial Diseases, Centerfj) Infectious Diseuses, Centers .o16 Disease Control, Atlanta, Georgia 303331; Epidemiologv Surveillunce Cetîter, Seereturirt oJfHealtli, Sao Pauzlo, S.P., Brazil2; Center for Biologics Evalation und Research, Food and Drug Administration, Bethesda, Murylund 20205'; and Health Division, Oregon Departinent of Huinan ...

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Suspected Brazilian Purpuric Fever, Brazilian Amazon Region

To the Editor: Brazilian purpuric fever (BPF), a Haemophilus aegyptius–caused febrile hemorrhagic illness of children that begins with conjunctivitis and has a case-fatality rate of 40%–90% (1,2), was fi rst recognized during a 1984 outbreak. Before June 2007, 69 cases were reported worldwide; 65 were from Brazil (1–3). To our knowledge, the disease had not been reported in the Amazon region un...

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Inflammatory response of Haemophilus influenzae biotype aegyptius causing Brazilian Purpuric Fever

The Brazilian Purpuric Fever (BPF) is a systemic disease with many clinical features of meningococcal sepsis and is usually preceded by purulent conjunctivitis. The illness is caused by Haemophilus influenza biogroup aegyptius, which was associated exclusively with conjunctivitis. In this work construction of the las gene, hypothetically responsible for this virulence, were fusioned with ermAM ...

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Pigmented purpuric dermatoses.

Pigmented purpuric dermatoses (PPD) are a group of histopathologically similar conditions that are primarily differentiated based on morphology. The basic pathological finding is a lymphocytic perivascular infiltrate with hemorrhage limited to the papillary dermis without fibrinoid necrosis of the vessels. The etiology is unknown; they run a chronic course and are fairly resistant to treatment....

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ژورنال

عنوان ژورنال: The Lancet

سال: 1867

ISSN: 0140-6736

DOI: 10.1016/s0140-6736(02)51893-6