Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Alasdair Geddes"'
Publikováno v:
Journal of Antimicrobial Chemotherapy. 75:2375-2375
Autor:
G.N. Rolinson, Alasdair Geddes
Publikováno v:
International Journal of Antimicrobial Agents. 29:3-8
This year (2007) marks the 50th anniversary of [corrected] discovery of 6-aminopenicillanic acid (6-APA), the precursor of all semi-synthetic penicillins [corrected] This review, by a scientist who played a major part in the discovery and a physician
Autor:
Alasdair Geddes, Kurt G. Naber
Publikováno v:
International journal of antimicrobial agents. 45(6)
Autor:
Alasdair Geddes
Publikováno v:
Journal of Antimicrobial Chemotherapy. 71:283-284
Autor:
Alasdair Geddes
Publikováno v:
Journal of Antimicrobial Chemotherapy. 72:1847-1847
Autor:
Alasdair Geddes
Publikováno v:
Journal of Antimicrobial Chemotherapy. 46:873-877
The late Paul Garrod, in whose honour this lecture is named, was 'the right man at the right time'. He seized the opportunities offered by the dawning of the chemotherapeutic era with vigour and enthusiasm and was a formidable link between the tradit
Grepafloxacin: an overview of antibacterial activity, pharmacokinetics, clinical efficacy and safety
Autor:
Alasdair Geddes
Publikováno v:
Expert Opinion on Investigational Drugs. 8:487-505
The treatment of respiratory tract infection is the most common reason for antibiotic prescribing. However, therapeutic options are diminishing as antibiotic resistance to penicillins and macrolides in key respiratory pathogens is increasing. As resi
Publikováno v:
Journal of Antimicrobial Chemotherapy. 37:135-144
A total of 686 adult patients with complicated urinary tract infections were enrolled in a double-blind, randomised, multicentre study to compare sparfloxacin (200 mg loading dose on day 1 followed by 100 mg daily) with ciprofloxacin (500 mg orally t
Publikováno v:
International Journal of Antimicrobial Agents. 2:203-230
Within the past decade several new fluoroquinolones (norfloxacin, enoxacin, ofloxacin, ciprofloxacin, pefloxacin, temafloxacin and lomefloxacin) have been introduced into therapy. All these agents share a broad spectrum of activity against a variety