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58 – Streptococcus group A vaccines

Karen L. Kotloff
- pp 1169-1175
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The article was published on 2013-01-01 and is currently open access. It has received 1 citations till now. The article focuses on the topics: Streptococcus.

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Citations
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The Serological Differentiation of Pathogenic and Non-Pathogenic Strains of Hemolytie Streptococci from Parturient Women.

TL;DR: The existence of two new serological groups of hemolytic streptococci, Groups F and G, is described, and the majority of strains isolated from the birth canal of women whose puerperium was afebrile were not members of Group A.
References
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Journal ArticleDOI

The global burden of group A streptococcal diseases

TL;DR: The need to reinforce current control strategies, develop new primary prevention strategies, and collect better data from developing countries for most diseases is highlighted, as GAS is an important cause of morbidity and mortality.
Journal ArticleDOI

Pathogenesis of Group A Streptococcal Infections

TL;DR: Group A streptococci are model extracellular gram-positive pathogens responsible for pharyngitis, impetigo, rheumatic fever, and acute glomerulonephritis, and an emerging theme is the dichotomy between skin and throat strains in their epidemiology and genetic makeup.
Journal ArticleDOI

A serological differentiation of human and other groups of hemolytic streptococci.

TL;DR: Five strains of hemolytic streptococci isolated from man, other animals, milk, and cheese have been classified into five groups, which bear a definite relationship to the sources of the cultures, each being chemically distinct and ser specific in the individual groups.
Journal ArticleDOI

Streptococcal M protein: molecular design and biological behavior.

TL;DR: Many of the approaches described in the elucidation of the M-protein structure may be applied for characterizing similar molecules in other microbial systems.
Journal ArticleDOI

Effectiveness of heptavalent pneumococcal conjugate vaccine in children younger than five years of age for prevention of pneumonia.

TL;DR: The heptavalent CRM197 pneumococcal conjugate vaccine was given to infants at 2, 4, 6 and 12 to 15 months of age in a randomized, double blind trial and was effective in reducing the risk of pneumonia in young children.