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Toplam kayıt 797, listelenen: 131-140
Escmid Dagger And Ecmm Double Dagger Joint Clinical Guidelines For The Diagnosis And Management Of Mucormycosis 2013
(Elsevier Sci Ltd, 2014)
These European Society for Clinical Microbiology and Infectious Diseases and European Confederation of Medical Mycology Joint Clinical Guidelines focus on the diagnosis and management of mucormycosis. Only a few of the ...
Escmid And Ecmm Joint Clinical Guidelines For The Diagnosis And Management Of Systemic Phaeohyphomycosis: Diseases Caused By Black Fungi
(Elsevier Sci Ltd, 2014)
The aetiological agents of many invasive fungal infections are saprobes and opportunistic pathogens. Some of these fungi are darkly pigmented due to melanin production and traditionally have been named dematiaceous'. The ...
Escmid And Ecmm Joint Guidelines On Diagnosis And Management Of Hyalohyphomycosis: Fusarium Spp., Scedosporium Spp. And Others
(Elsevier Sci Ltd, 2014)
Mycoses summarized in the hyalohyphomycosis group are heterogeneous, defined by the presence of hyaline (non-dematiaceous) hyphae. The number of organisms implicated in hyalohyphomycosis is increasing and the most clinically ...
Escmid* Guideline For The Diagnosis And Management Of Candida Diseases 2012: Diagnostic Procedures
(Elsevier Sci Ltd, 2012)
Clin Microbiol Infect 2012; 18 (Suppl. 7): 918 Abstract As the mortality associated with invasive Candida infections remains high, it is important to make optimal use of available diagnostic tools to initiate antifungal ...
Epidemiologic Trends In Hbv Infections At A Reference Centre In Turkey: An 11-Year Retrospective Analysis
(Elsevier Espana, 2012)
Objective. To identify changes in hepatitis B epidemiology after the implementation of the nationwide vaccination program in Turkey, hepatitis B virus (HBV) and related tests performed over a period of 11 years (2000-2010) ...
Rationale, Design and Objectives of Aregpkd, A European Arpkd Registry Study
(2015)
Background Autosomal recessive polycystic kidney disease (ARPKD) is a rare but frequently severe disorder that is typically characterized by cystic kidneys and congenital hepatic fibrosis but displays pronounced phenotypic ...