cefotaxime and Genetic-Diseases--Inborn

cefotaxime has been researched along with Genetic-Diseases--Inborn* in 1 studies

1 other study(ies) available for cefotaxime and Genetic-Diseases--Inborn

Article	Year
C2 deficiency primary meningococcal arthritis of the elbow by Neisseria meningitidis serogroup Y in a 12-year old girl. Infection, 2007, Volume: 35, Issue:4 Topics: Arthritis, Infectious; Cefotaxime; Child; Complement C2; Female; Genetic Diseases, Inborn; Humans; Meningococcal Infections; Microbial Sensitivity Tests; Neisseria meningitidis; Rifampin; Serotyping	2007