Manual of Clinical MicrobiologyAlbert Balows, American Society for Microbiology First published in 1970, previous edition in 1985. MCM5 is enlarged and restructured to keep pace with new developments and technology. Users must have knowledge of the fundamentals of microbiology and possess basic laboratory skills. Operational and organizational chapters address topics ranging from collecting and managing clinical specimens to selecting the best methodological approach for determining strain identity. Subsequent chapters deal with specific microorganisms as etiologic agents and with the clinical microbiologic laboratory in various treatment and research functions. Member price, $64. Annotation copyrighted by Book News, Inc., Portland, OR |
From inside the book
Results 1-3 of 90
Page 142
... toxin is determined by increased tyrosinase ac- tivity and accumulation of melanin in the B16 cells . ST ST are small peptides that withstand temperatures up to 100 ° C . They are produced by a variety of bacteria , most notably E. coli ...
... toxin is determined by increased tyrosinase ac- tivity and accumulation of melanin in the B16 cells . ST ST are small peptides that withstand temperatures up to 100 ° C . They are produced by a variety of bacteria , most notably E. coli ...
Page 506
... toxins are detected by using toxicity and toxin - antiserum neu- tralization tests in mice ( 26 ) . Most infections of humans involving C. perfringens are caused by type A strains . C. perfringens type C is the only other toxin type en ...
... toxins are detected by using toxicity and toxin - antiserum neu- tralization tests in mice ( 26 ) . Most infections of humans involving C. perfringens are caused by type A strains . C. perfringens type C is the only other toxin type en ...
Page 512
... toxins have been developed , but they have not yet enjoyed routine use in clinical laboratories ( 105 ) . One commercial membrane - bound solid - phase ELISA for toxin has been evaluated ( 110 ) . Gram stain of fecal smears ( 85 ) and ...
... toxins have been developed , but they have not yet enjoyed routine use in clinical laboratories ( 105 ) . One commercial membrane - bound solid - phase ELISA for toxin has been evaluated ( 110 ) . Gram stain of fecal smears ( 85 ) and ...
Contents
Specimen Collection and Handling HENRY D ISENBERG JOHN A WASHINGTON II GARY V | 15 |
Microscopy KIMBERLE CHAPINROBERTSON AND STEPHEN C EDBERG | 29 |
Quality Assurance in the Clinical Microbiology Laboratory RAYMOND C BARTLETT | 36 |
Copyright | |
111 other sections not shown
Common terms and phrases
acid aerobic Aeromonas agar plates agents agglutination anaerobic antibiotic antibody antigen antimicrobial assay aureus Bacillus bacteremia bacteria Bacteriol biochemical biotype blood agar blood culture broth Campylobacter catalase caused cells characteristics chemical Clin clinical laboratory clinical microbiology clinical specimens coli colonies containing detection diagnosis differentiation disease disinfection Enterobacteriaceae enterococci enzyme epidemiologic esculin fermentation fluid genus germicides glucose Gram stain gram-negative growth Haemophilus hospital human hydrolysis identification incubation infections inoculated isolated Legionella mannitol medium meningitis methods microbial Microbiol microbiology microorganisms Motility Mycobacterium negative Neisseria Nocardia nosocomial nosocomial infections organisms oxidase pathogens patients pertussis plasmid pneumoniae polymyxin positive present probes procedures produce protein Pseudomonas reaction reagents reported resistance Salmonella sample sensitivity serological serotypes serum Shigella smear species staphylococci sterile strains streptococci subsp substrate susceptibility testing swab Table techniques tion tissue toxin tube tuberculosis urease usually vancomycin Vibrio virus