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Advancing the Management Of Hereditary Angioedema
Hereditary angioedema (HAE) is a rare but potentially life-threatening genetic disease caused by functional C1-inhibitor (C1-INH) deficiency and characterized by recurrent episodes of severe, localized edema of the skin, gastrointestinal mucosa, and upper respiratory tract that do not respond to treatment with antihistamines or corticosteroids.
To request a free hard copy of this Special Report article, please email your full name, mailing address, and institution to infectiousdisease@mcmahonmed.com
JUNE, 2010 |
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Guidelines in the Treatment of Methicillin-Resistant Staphylococcus aureus
Staphylococcus aureus is a significant cause of disease in humans that can cause life-threatening infection. Although staphylococcal disease is most often associated with skin and soft tissue infections (SSTIs), its manifestations are myriad and include syndromes with low morbidity and mortality, such as folliculitis and food poisoning, and fatal systemic illnesses, such as endocarditis and toxic shock syndrome.
To request a free hard copy of this Special Report article, please email your full name, mailing address, and institution to infectiousdisease@mcmahonmed.com
SEPTEMBER, 2009 |
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