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Original Paper

Non-invasive Diagnostic of Helicobacter pylori in Stools by Nested-qPCR

María I. Taborda, Gisela Aquea, Yenny Nilo, Karla Salvatierra, Nicolás López, Sergio López, Gustavo Bresky, Juan A. Madariaga, Vittorio Zaffiri, Sergio Häberle, Giuliano Bernal

Polish Journal of Microbiology , ISSUE 1, 11–18


Evidence for Infections by the Same Strain of Beta 2-toxigenic Clostridium perfringens Type A Acquired in One Hospital Ward

strains in 2015, two patients carried the strains that had the cpb2 gene, indicated an extremely severe course of these infections (Brzychczy-Włoch et al. 2016). The presence of the gene for β2-toxin in C. perfringens strains causing soft tissue infections in humans requires further observation, which could be assisted by the application of genetic analysis of this pathogen in every clinical case involving C. perfringens. Molecular diagnostics of the strains isolated also allowed their final


Polish Journal of Microbiology , ISSUE 3, 323–329


Morphological and molecular characterizations of Heterodera oryzae in Korea

elachista (MH144207, KC618472, and KC618473), H. guangdongesis (MF425735), H. cyperi (MG857126), and H. monthi (MH144208) were 2.7, 14.7, 12.3, and 20.4%, respectively. From the results of COI sequences, we concluded that SG936 and SG153 populations were not H. elachista, but are just closely related species. Combining morphological and molecular diagnostics, SG936 and SG153 samples were identified as H. oryzae. This was the first time to study molecular characteristics of H. oryzae. Discussion Using

Rose Mwesige, Eun-Hwa Kim, Eun-Hyung Park, Hyoung-Rai Ko

Journal of Nematology , 1–12


The potential of blood group genotyping for transfusion medicine practice

Molecular diagnostics is the fastest growing area of clinical laboratory medicine.  The ability to rapidly amplify genes of bacterial, viral, or human origin, and the development of DNA array platforms, are driving a technology revolution in the clinical laboratory.  A DNA-based testing approach is particularly applicable to blood bank and transfusion medicine for rapid, cost-effective antigen typing.  Experience with DNA-based methods during the past decade has shown that these

Connie M. Westhoff

Immunohematology , ISSUE 4, 190–195

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