ライフサイエンスコーパス: laboratory diagnosis

1 in ocular specimens by NAAT was verified for laboratory diagnosis.

2 uary 2010 and January 2012 were enrolled for laboratory diagnosis.

3 en is a suitable antigen in an ELISA for the laboratory diagnosis and epidemiological study of HGE.

4 Laboratory diagnosis and genetic counseling for AS are c

5 e control and of confirmatory assays for the laboratory diagnosis and verification of H5 virus infect

6 criteria with electronic medical records of laboratory, diagnosis, and pharmacy information.

7 Blood cultures are the mainstay of laboratory diagnosis, but lack sensitivity due to the lo

8 of dengue provides the framework for dengue laboratory diagnosis by using a single serum specimen.

9 The mainstay of laboratory diagnosis for Lyme disease is two-tiered sero

10 Laboratory diagnosis has played a critical role in the G

11 Laboratory diagnosis has traditionally been by the indir

12 uperseded culture as the preferred method of laboratory diagnosis; however, neither culture nor PCR i

13 tutes of Health (NIH), made the confirmatory laboratory diagnosis in 35 multiple sclerosis (MS) patie

14 The gold standards for laboratory diagnosis include demonstration of yeast on p

15 ; in 35%, all cultures were negative and the laboratory diagnosis indeterminate.

16 nge of clinical symptoms, early and accurate laboratory diagnosis is essential for appropriate patien

17 Once laboratory diagnosis is made, pathogen-specific antimicr

18 A laboratory diagnosis is required to confirm cases of cry

19 Confirmation of Acanthamoeba keratitis by laboratory diagnosis is the first step in the treatment

20 0%-15% of people over the age of 60, and the laboratory diagnosis is usually based on low serum vitam

21 that the pan-EV MAb mix can be used for the laboratory diagnosis of a wide range of EV infections.

22 The tests were standardized for laboratory diagnosis of arboviral infections, with the i

23 A variety of methods have emerged for the laboratory diagnosis of aspirin resistance.

24 Laboratory diagnosis of Borrelia burgdorferi is routinel

25 In this point-counterpoint on the laboratory diagnosis of C. difficile infection, we have

26 nism, there has been renewed interest in the laboratory diagnosis of C. difficile infection.

27 e considered the new "gold standard" for the laboratory diagnosis of C. trachomatis infections.

28 The conventional approach to the laboratory diagnosis of Campylobacter enteritis is based

29 Until recently, the laboratory diagnosis of central nervous system (CNS) inf

30 blished an initial Point-Counterpoint on the laboratory diagnosis of Clostridium difficile infection

31 Rapid laboratory diagnosis of Clostridium difficile-associated

32 nsidered an emerging "gold standard" for the laboratory diagnosis of CNS infections with this virus.

33 Symptoms of STIs were recorded, and laboratory diagnosis of common STI pathogens was conduct

34 The clinical laboratory diagnosis of cutaneous anthrax is generally e

35 We show that a multipronged approach to the laboratory diagnosis of dengue infections can be used to

36 l and improved diagnostics, particularly for laboratory diagnosis of earlier stages of infection.

37 ith Borrelia antigens could be useful in the laboratory diagnosis of early Lyme disease.

38 Laboratory diagnosis of Ebola hemorrhagic fever (EHF) is

39 s a safe, sensitive, and specific method for laboratory diagnosis of EHF and should be useful for EHF

40 ide a rapid and reliable alternative for the laboratory diagnosis of enteric infections with C. jejun

41 These findings will assist with the rapid laboratory diagnosis of enteritis in puppies and highlig

42 The "gold standard" for laboratory diagnosis of enteroviruses is cell culture is

43 Patients with confirmed clinical and laboratory diagnosis of FFI have been retrospectively re

44 n appropriate alternative to culture for the laboratory diagnosis of GAS pharyngitis in patients for

45 ke it an effective assay system for clinical laboratory diagnosis of HCV and HBV infections.

46 vels in chromosomal integration may confound laboratory diagnosis of HHV-6 infection and should be gi

47 Laboratory diagnosis of HSV in cutaneous or mucocutaneou

48 system and could replace the latter for the laboratory diagnosis of HSV infections using LightCycler

49 outine implementation of this technology for laboratory diagnosis of HSV infections.

50 such as CPAF, TARP, and SINC may improve the laboratory diagnosis of human and animal C abortus infec

51 a PCR-based assay for the rapid and specific laboratory diagnosis of human brucellosis directly from

52 Laboratory diagnosis of human ehrlichioses is routinely

53 of emerging tick-borne pathogens and improve laboratory diagnosis of human infections.

54 ained health-care workers were compared with laboratory diagnosis of infection.

55 examining the impact of specimen type on the laboratory diagnosis of influenza A and B.

56 immunochromatographic antigen testing in the laboratory diagnosis of influenza A virus infection duri

57 The current standard for laboratory diagnosis of Lyme disease in the United State

58 f both solid and liquid culture media in the laboratory diagnosis of nonviral keratitis.

59 Clinical and laboratory diagnosis of partial deficiencies during asym

60 ation directly and indirectly related to the laboratory diagnosis of PIDs.

61 Although laboratory diagnosis of respiratory viruses has been wid

62 Laboratory diagnosis of SFTS was made by isolation/genom

63 f syndromic diagnosis of STIs, compared with laboratory diagnosis of STIs, and evaluated the associat

64 standardized PCR method is available for the laboratory diagnosis of the pertussis syndrome.

65 The management and laboratory diagnosis of these infections pose unique cha

66 , findings that are relevant to the accurate laboratory diagnosis of this genodermatosis by skin immu

67 rs discuss recent trends in the clinical and laboratory diagnosis of this syndrome that are of releva

68 mplementation of this technology for routine laboratory diagnosis of this viral infection.

69 itute (TSL-PAMFRI) has been dedicated to the laboratory diagnosis of Toxoplasma gondii infection and

70 Laboratory diagnosis of tuberculosis is often difficult.

71 nd an ESAT-6 intracellular stain improve the laboratory diagnosis of tuberculous meningitis.

72 Currently, the laboratory diagnosis of typhoid fever is dependent upon

73 Laboratory diagnosis of typhoid fever requires isolation

74 evaluation, as 11-16% of them will meet the laboratory diagnosis of von Willebrand disease.

75 The laboratory diagnosis of vWD and its several variants is

76 Currently, the laboratory diagnosis of Zika virus (ZIKV) infection is p

77 in blood films remains the gold standard for laboratory diagnosis, rapid antigen tests and nucleic ac

78 The laboratory diagnosis relies on the spectrophotometric as

79 In 93% of these cases (229 of 246) the laboratory diagnosis was made by detection of M. tubercu