ライフサイエンスコーパス: laboratory diagnosis

1 e study of Buruli ulcer pathogenesis and for laboratory diagnosis.

2 gy of CDI among those with IBD by DAD versus laboratory diagnosis.

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

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

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

6 Laboratory diagnosis and genetic counseling for AS are c

7 thods are needed to improve the clinical and laboratory diagnosis and management of PCP.

8 rouped patients according to their arbovirus laboratory diagnosis and then compared demographic and c

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

10 ingococcal urethritis, emergence of US_NmUC, laboratory diagnosis, and clinical treatment are all exp

11 10 working groups looked closely at imaging, laboratory diagnosis, and special populations at risk of

12 ned to 1 of the following 4 categories using laboratory, diagnosis, and chart review data: definite r

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

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

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

16 Early laboratory diagnosis can help guide physicians to provid

17 Rapid laboratory diagnosis can help initiate early effective a

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

19 Laboratory diagnosis has historically relied on serologi

20 Laboratory diagnosis has played a critical role in the G

21 Laboratory diagnosis has relied on a two-tier serologic

22 Laboratory diagnosis has traditionally been by the indir

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

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

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

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

27 Laboratory diagnosis is based on coagulation abnormaliti

28 inical management and outbreak response, yet laboratory diagnosis is complex, costly, and lacks conse

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

30 Once laboratory diagnosis is made, pathogen-specific antimicr

31 A laboratory diagnosis is required to confirm cases of cry

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

33 0%-15% of people over the age of 60, and the laboratory diagnosis is usually based on low serum vitam

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

35 All patients with clinical and laboratory diagnosis of acute pyelonephritis, who were r

36 irst single-tier serologic test suitable for laboratory diagnosis of all stages of Lyme disease.

37 The laboratory diagnosis of antiviral resistance is a quickl

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

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

40 Laboratory diagnosis of blastomycosis relies on a combin

41 Laboratory diagnosis of Borrelia burgdorferi is routinel

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

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

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

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

46 However, the laboratory diagnosis of CDI, primarily done by nucleic a

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

48 provide an initial evidence base to improve laboratory diagnosis of Chagas disease in the United Sta

49 The laboratory diagnosis of Clostridioides difficile infecti

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

51 Rapid laboratory diagnosis of Clostridium difficile-associated

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

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

54 97 patients with a laboratory diagnosis of COVID-19 infection, and 50 age-m

55 The clinical laboratory diagnosis of cutaneous anthrax is generally e

56 ty and utility of UV fluorescence to improve laboratory diagnosis of cyclosporiasis.

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

58 Laboratory diagnosis of dengue is essential for providin

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

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

61 Laboratory diagnosis of Ebola hemorrhagic fever (EHF) is

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

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

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

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

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

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

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

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

70 Laboratory diagnosis of HSV in cutaneous or mucocutaneou

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

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

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

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

75 Laboratory diagnosis of human ehrlichioses is routinely

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

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

78 covers current issues and challenges for the laboratory diagnosis of infections caused by severe acut

79 assay as a novel tool for rapid and accurate laboratory diagnosis of infectious uveitis.

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

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

82 2-tiered (STT) algorithm recommended for the laboratory diagnosis of Lyme disease if they perform wit

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

84 The laboratory diagnosis of Lyme disease relies upon serolog

85 The laboratory diagnosis of Lyme disease relies upon the det

86 n proper specimen selection not only for the laboratory diagnosis of M. genitalium but also macrolide

87 Laboratory diagnosis of microbial agents associated with

88 With improvement in laboratory diagnosis of Mycoplasmoides genitalium infect

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

90 us treatments in patients with a clinical or laboratory diagnosis of OMMP, were analyzed with multiva

91 Clinical and laboratory diagnosis of partial deficiencies during asym

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

93 s were women aged older than 18 years with a laboratory diagnosis of primary breast cancer requiring

94 Although laboratory diagnosis of respiratory viruses has been wid

95 d together) or placebo within 3 days after a laboratory diagnosis of severe acute respiratory syndrom

96 We explore ways to reduce errors in laboratory diagnosis of severe acute respiratory syndrom

97 Laboratory diagnosis of SFTS was made by isolation/genom

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

99 traditional or reverse algorithm?" Improved laboratory diagnosis of syphilis is an important element

100 . pallidum TMA) has the potential to improve laboratory diagnosis of syphilis, particularly in patien

101 xpert panel generated "key questions" in the laboratory diagnosis of syphilis.

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

103 Traditional methods for the laboratory diagnosis of these infections are time-consum

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

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

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

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

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

109 Laboratory diagnosis of tuberculosis is often difficult.

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

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

112 Laboratory diagnosis of typhoid fever requires isolation

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

114 The laboratory diagnosis of vWD and its several variants is

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

116 ort systems, laboratory procurement systems, laboratory diagnosis, quality management, and laboratory

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

118 The laboratory diagnosis relies on the spectrophotometric as

119 mpox cases and deaths, based on clinical or laboratory diagnosis, that were reported to the Africa C

120 la presentation and an increased reliance on laboratory diagnosis to confirm suspected cases.

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

122 se was associated with CDI using DAD but not laboratory diagnosis, whereas corticosteroid exposure wa