Utility of polymerase chain reaction for assessment of onychomycosis during topical therapy

Background Increased detection of fungi including non‐dermatophyte molds (NDMs) using polymerase chain reaction (PCR) methods is well‐established. However, the use of PCR to evaluate ongoing onychomycosis treatment outcome has not been investigated. Methods Nail samples from 28 patients receiving to...

Full description

Saved in:
Bibliographic Details
Published inInternational journal of dermatology Vol. 61; no. 11; pp. 1385 - 1389
Main Authors Gupta, Aditya K., Cooper, Elizabeth A., Summerbell, Richard C., Nakrieko, Kerry‐Ann
Format Journal Article
LanguageEnglish
Published Hoboken Blackwell Publishing Ltd 01.11.2022
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Background Increased detection of fungi including non‐dermatophyte molds (NDMs) using polymerase chain reaction (PCR) methods is well‐established. However, the use of PCR to evaluate ongoing onychomycosis treatment outcome has not been investigated. Methods Nail samples from 28 patients receiving topical efinaconazole were evaluated by both KOH/culture and PCR methods across the study period. Detection of microorganisms by PCR was compared to the culture at baseline and end of study at month 24 (M24). Fungal detection by both methods was evaluated with respect to clinical cure observed as 100% visual clearance of the target toenail. Results By culture, all 28 subjects were dermatophyte‐positive at pre‐treatment; only 4/28 also exhibited an NDM microorganism. According to PCR, 24/28 subjects were dermatophyte‐positive pre‐treatment, with 25/28 also exhibiting NDMs. At M24, 18/28 (64.3%) participants had negative KOH/culture results, in contrast to 4/28 (14.3%) negative PCR results. PCR showed higher rates of NDM detection than the culture at baseline as well as M24. Calculations to compare the diagnostic utility of KOH/culture versus PCR found that positive tests with both methods reliably indicate the presence of onychomycosis, but negative PCR correlated better with onychomycosis cure than did KOH/culture. Discussion PCR confirmed a high presence of NDMs pre‐treatment, and continued presence of NDMs to M24, with unknown significance requiring further investigation. Though both KOH/culture and PCR have diagnostic limitations, PCR showed better overall utility than culture in predicting onychomycosis topical treatment outcome and should be more strongly considered for evaluation of topical therapies.
AbstractList BackgroundIncreased detection of fungi including non‐dermatophyte molds (NDMs) using polymerase chain reaction (PCR) methods is well‐established. However, the use of PCR to evaluate ongoing onychomycosis treatment outcome has not been investigated.MethodsNail samples from 28 patients receiving topical efinaconazole were evaluated by both KOH/culture and PCR methods across the study period. Detection of microorganisms by PCR was compared to the culture at baseline and end of study at month 24 (M24). Fungal detection by both methods was evaluated with respect to clinical cure observed as 100% visual clearance of the target toenail.ResultsBy culture, all 28 subjects were dermatophyte‐positive at pre‐treatment; only 4/28 also exhibited an NDM microorganism. According to PCR, 24/28 subjects were dermatophyte‐positive pre‐treatment, with 25/28 also exhibiting NDMs. At M24, 18/28 (64.3%) participants had negative KOH/culture results, in contrast to 4/28 (14.3%) negative PCR results. PCR showed higher rates of NDM detection than the culture at baseline as well as M24. Calculations to compare the diagnostic utility of KOH/culture versus PCR found that positive tests with both methods reliably indicate the presence of onychomycosis, but negative PCR correlated better with onychomycosis cure than did KOH/culture.DiscussionPCR confirmed a high presence of NDMs pre‐treatment, and continued presence of NDMs to M24, with unknown significance requiring further investigation. Though both KOH/culture and PCR have diagnostic limitations, PCR showed better overall utility than culture in predicting onychomycosis topical treatment outcome and should be more strongly considered for evaluation of topical therapies.
Background Increased detection of fungi including non‐dermatophyte molds (NDMs) using polymerase chain reaction (PCR) methods is well‐established. However, the use of PCR to evaluate ongoing onychomycosis treatment outcome has not been investigated. Methods Nail samples from 28 patients receiving topical efinaconazole were evaluated by both KOH/culture and PCR methods across the study period. Detection of microorganisms by PCR was compared to the culture at baseline and end of study at month 24 (M24). Fungal detection by both methods was evaluated with respect to clinical cure observed as 100% visual clearance of the target toenail. Results By culture, all 28 subjects were dermatophyte‐positive at pre‐treatment; only 4/28 also exhibited an NDM microorganism. According to PCR, 24/28 subjects were dermatophyte‐positive pre‐treatment, with 25/28 also exhibiting NDMs. At M24, 18/28 (64.3%) participants had negative KOH/culture results, in contrast to 4/28 (14.3%) negative PCR results. PCR showed higher rates of NDM detection than the culture at baseline as well as M24. Calculations to compare the diagnostic utility of KOH/culture versus PCR found that positive tests with both methods reliably indicate the presence of onychomycosis, but negative PCR correlated better with onychomycosis cure than did KOH/culture. Discussion PCR confirmed a high presence of NDMs pre‐treatment, and continued presence of NDMs to M24, with unknown significance requiring further investigation. Though both KOH/culture and PCR have diagnostic limitations, PCR showed better overall utility than culture in predicting onychomycosis topical treatment outcome and should be more strongly considered for evaluation of topical therapies.
Increased detection of fungi including non-dermatophyte molds (NDMs) using polymerase chain reaction (PCR) methods is well-established. However, the use of PCR to evaluate ongoing onychomycosis treatment outcome has not been investigated.BACKGROUNDIncreased detection of fungi including non-dermatophyte molds (NDMs) using polymerase chain reaction (PCR) methods is well-established. However, the use of PCR to evaluate ongoing onychomycosis treatment outcome has not been investigated.Nail samples from 28 patients receiving topical efinaconazole were evaluated by both KOH/culture and PCR methods across the study period. Detection of microorganisms by PCR was compared to the culture at baseline and end of study at month 24 (M24). Fungal detection by both methods was evaluated with respect to clinical cure observed as 100% visual clearance of the target toenail.METHODSNail samples from 28 patients receiving topical efinaconazole were evaluated by both KOH/culture and PCR methods across the study period. Detection of microorganisms by PCR was compared to the culture at baseline and end of study at month 24 (M24). Fungal detection by both methods was evaluated with respect to clinical cure observed as 100% visual clearance of the target toenail.By culture, all 28 subjects were dermatophyte-positive at pre-treatment; only 4/28 also exhibited an NDM microorganism. According to PCR, 24/28 subjects were dermatophyte-positive pre-treatment, with 25/28 also exhibiting NDMs. At M24, 18/28 (64.3%) participants had negative KOH/culture results, in contrast to 4/28 (14.3%) negative PCR results. PCR showed higher rates of NDM detection than the culture at baseline as well as M24. Calculations to compare the diagnostic utility of KOH/culture versus PCR found that positive tests with both methods reliably indicate the presence of onychomycosis, but negative PCR correlated better with onychomycosis cure than did KOH/culture.RESULTSBy culture, all 28 subjects were dermatophyte-positive at pre-treatment; only 4/28 also exhibited an NDM microorganism. According to PCR, 24/28 subjects were dermatophyte-positive pre-treatment, with 25/28 also exhibiting NDMs. At M24, 18/28 (64.3%) participants had negative KOH/culture results, in contrast to 4/28 (14.3%) negative PCR results. PCR showed higher rates of NDM detection than the culture at baseline as well as M24. Calculations to compare the diagnostic utility of KOH/culture versus PCR found that positive tests with both methods reliably indicate the presence of onychomycosis, but negative PCR correlated better with onychomycosis cure than did KOH/culture.PCR confirmed a high presence of NDMs pre-treatment, and continued presence of NDMs to M24, with unknown significance requiring further investigation. Though both KOH/culture and PCR have diagnostic limitations, PCR showed better overall utility than culture in predicting onychomycosis topical treatment outcome and should be more strongly considered for evaluation of topical therapies.DISCUSSIONPCR confirmed a high presence of NDMs pre-treatment, and continued presence of NDMs to M24, with unknown significance requiring further investigation. Though both KOH/culture and PCR have diagnostic limitations, PCR showed better overall utility than culture in predicting onychomycosis topical treatment outcome and should be more strongly considered for evaluation of topical therapies.
Author Nakrieko, Kerry‐Ann
Gupta, Aditya K.
Cooper, Elizabeth A.
Summerbell, Richard C.
Author_xml – sequence: 1
  givenname: Aditya K.
  orcidid: 0000-0002-8664-7723
  surname: Gupta
  fullname: Gupta, Aditya K.
  email: agupta@mediproberesearch.com
  organization: Mediprobe Research Inc
– sequence: 2
  givenname: Elizabeth A.
  orcidid: 0000-0002-1121-5619
  surname: Cooper
  fullname: Cooper, Elizabeth A.
  organization: Mediprobe Research Inc
– sequence: 3
  givenname: Richard C.
  orcidid: 0000-0002-3395-6514
  surname: Summerbell
  fullname: Summerbell, Richard C.
  organization: University of Toronto
– sequence: 4
  givenname: Kerry‐Ann
  orcidid: 0000-0002-9317-7141
  surname: Nakrieko
  fullname: Nakrieko, Kerry‐Ann
  organization: Mediprobe Research Inc
BookMark eNp1kD1PwzAURS0EEqUw8A8sscCQ1l9xkhHxjSqx0InBchyHukrsYLtC-fe4tFMFb3l60rlXT-cMHFtnNQCXGM1wmrlZNzPMCcNHYIIpzzPGKTkGE4QwziqUV6fgLIR1OinBbAI-ltF0Jo7QtXBw3dhrL4OGaiWNhV5LFY2zsHUeyhB0CL22ccs6O6qV60flggmw2XhjP2F0g1Gyg3GVWobxHJy0sgv6Yr-nYPn48H73nC3enl7ubheZIhzhjKmaliWrZI54o5lqS1opXteIa1pUrG1aTooaVSUtypryoqAYI0VQw3S6dEmn4HrXO3j3tdEhit4EpbtOWu02QRDOcZXnlKGEXh2ga7fxNn0nSEFYgUhOSKLmO0p5F4LXrVAmyq2J6KXpBEZiK1sk2eJXdkrcHCQGb3rpxz_Zffu36fT4PyheXu93iR_-4JAi
CitedBy_id crossref_primary_10_1007_s00105_023_05265_9
crossref_primary_10_1055_a_1857_2774
crossref_primary_10_1111_jdv_19644
crossref_primary_10_3390_microbiolres16020051
crossref_primary_10_1007_s40257_024_00848_1
crossref_primary_10_1080_14656566_2024_2416924
crossref_primary_10_1111_jdv_19217
crossref_primary_10_1093_bjd_ljad070
crossref_primary_10_3390_jof9060671
Cites_doi 10.1111/bjd.12594
10.1016/j.jaad.2011.02.038
10.3109/13693781003743130
10.1111/ajd.12027
10.1128/JCM.39.6.2115-2121.2001
10.1128/JCM.39.2.685-690.2001
10.1128/JCM.37.4.931-936.1999
10.7547/15-136
10.1111/j.1365-2133.2009.09291.x
10.1111/j.1346-8138.2009.00624.x
10.1111/j.1365-2133.2008.08805.x
10.3389/fpubh.2017.00307
10.1111/j.1365-2133.2009.09249.x
10.1371/journal.pone.0239648
ContentType Journal Article
Copyright 2022 the International Society of Dermatology.
International Journal of Dermatology © 2022 International Society of Dermatology
Copyright_xml – notice: 2022 the International Society of Dermatology.
– notice: International Journal of Dermatology © 2022 International Society of Dermatology
DBID AAYXX
CITATION
7T5
7U7
C1K
H94
K9.
NAPCQ
7X8
DOI 10.1111/ijd.16241
DatabaseName CrossRef
Immunology Abstracts
Toxicology Abstracts
Environmental Sciences and Pollution Management
AIDS and Cancer Research Abstracts
ProQuest Health & Medical Complete (Alumni)
Nursing & Allied Health Premium
MEDLINE - Academic
DatabaseTitle CrossRef
AIDS and Cancer Research Abstracts
ProQuest Health & Medical Complete (Alumni)
Nursing & Allied Health Premium
Immunology Abstracts
Toxicology Abstracts
Environmental Sciences and Pollution Management
MEDLINE - Academic
DatabaseTitleList AIDS and Cancer Research Abstracts

MEDLINE - Academic
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1365-4632
EndPage 1389
ExternalDocumentID 10_1111_ijd_16241
IJD16241
Genre meetingReport
GroupedDBID ---
.3N
.GA
.GJ
.Y3
05W
0R~
10A
1OB
1OC
29J
31~
33P
36B
3O-
3SF
4.4
50Y
50Z
51W
51X
52M
52N
52O
52P
52R
52S
52T
52U
52V
52W
52X
53G
5GY
5HH
5LA
5RE
5VS
66C
702
7PT
8-0
8-1
8-3
8-4
8-5
8UM
930
A01
A03
AAESR
AAEVG
AAHHS
AAHQN
AAIPD
AAMNL
AANHP
AANLZ
AAONW
AAQQT
AASGY
AAXRX
AAYCA
AAZKR
ABCQN
ABCUV
ABEML
ABJNI
ABPVW
ABQWH
ABXGK
ACAHQ
ACBWZ
ACCFJ
ACCZN
ACGFO
ACGFS
ACGOF
ACMXC
ACPOU
ACPRK
ACRPL
ACSCC
ACXBN
ACXQS
ACYXJ
ADBBV
ADBTR
ADEOM
ADIZJ
ADKYN
ADMGS
ADNMO
ADOZA
ADXAS
ADZMN
ADZOD
AEEZP
AEGXH
AEIGN
AEIMD
AENEX
AEQDE
AEUQT
AEUYR
AFBPY
AFEBI
AFFNX
AFFPM
AFGKR
AFPWT
AFRAH
AFWVQ
AFZJQ
AHBTC
AHEFC
AIACR
AIAGR
AITYG
AIURR
AIWBW
AJBDE
ALAGY
ALMA_UNASSIGNED_HOLDINGS
ALUQN
ALVPJ
AMBMR
AMYDB
ATUGU
AZBYB
AZFZN
AZVAB
BAFTC
BDRZF
BFHJK
BHBCM
BMXJE
BROTX
BRXPI
BY8
C45
CAG
COF
CS3
CYRXZ
D-6
D-7
D-E
D-F
DC6
DCZOG
DPXWK
DR2
DRFUL
DRMAN
DRSTM
DU5
EBS
EJD
EMOBN
ESX
EX3
F00
F01
F04
F5P
FEDTE
FUBAC
FZ0
G-S
G.N
GODZA
H.X
HF~
HGLYW
HVGLF
HZI
HZ~
IHE
IX1
J0M
J5H
K48
KBYEO
L7B
LATKE
LC2
LC3
LEEKS
LH4
LITHE
LOXES
LP6
LP7
LUTES
LW6
LYRES
MEWTI
MK4
MRFUL
MRMAN
MRSTM
MSFUL
MSMAN
MSSTM
MXFUL
MXMAN
MXSTM
N04
N05
N9A
NF~
O66
O9-
OIG
OVD
P2P
P2W
P2X
P2Z
P4B
P4D
PALCI
Q.N
Q11
QB0
R.K
RIWAO
RJQFR
ROL
RX1
SAMSI
SUPJJ
TEORI
UB1
V8K
W8V
W99
WBKPD
WHWMO
WIH
WIJ
WIK
WOHZO
WOW
WQJ
WRC
WUP
WVDHM
WXI
WXSBR
XG1
YFH
YOC
YUY
ZGI
ZXP
ZZTAW
~IA
~WT
AAYXX
AEYWJ
AGHNM
AGQPQ
AGYGG
CITATION
7T5
7U7
AAMMB
AEFGJ
AGXDD
AIDQK
AIDYY
C1K
H94
K9.
NAPCQ
7X8
ID FETCH-LOGICAL-c2601-4cb38849a506de4cf839c6bb06e3794fdf627b098378b36773110c20d4e367e83
IEDL.DBID DR2
ISSN 0011-9059
1365-4632
IngestDate Fri Jul 11 15:39:26 EDT 2025
Sun Jul 13 03:59:12 EDT 2025
Thu Apr 24 23:11:45 EDT 2025
Tue Jul 01 04:25:29 EDT 2025
Wed Jan 22 16:23:54 EST 2025
IsPeerReviewed true
IsScholarly true
Issue 11
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c2601-4cb38849a506de4cf839c6bb06e3794fdf627b098378b36773110c20d4e367e83
Notes Conflict of interest: None.
Funding source: None.
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ORCID 0000-0002-8664-7723
0000-0002-1121-5619
0000-0002-9317-7141
0000-0002-3395-6514
PQID 2724702522
PQPubID 5776
PageCount 1389
ParticipantIDs proquest_miscellaneous_2661955340
proquest_journals_2724702522
crossref_citationtrail_10_1111_ijd_16241
crossref_primary_10_1111_ijd_16241
wiley_primary_10_1111_ijd_16241_IJD16241
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate November 2022
2022-11-00
20221101
PublicationDateYYYYMMDD 2022-11-01
PublicationDate_xml – month: 11
  year: 2022
  text: November 2022
PublicationDecade 2020
PublicationPlace Hoboken
PublicationPlace_xml – name: Hoboken
PublicationTitle International journal of dermatology
PublicationYear 2022
Publisher Blackwell Publishing Ltd
Publisher_xml – name: Blackwell Publishing Ltd
References 2017; 5
2009; 36
2021; 26
2010; 48
2020; 1
2013; 54
2009; 160
1999; 37
2020; 15
2009; 161
2014; 170
2001; 39
2012; 66
2017; 107
e_1_2_5_15_1
e_1_2_5_14_1
e_1_2_5_17_1
Foley K (e_1_2_5_18_1) 2020; 1
e_1_2_5_9_1
e_1_2_5_16_1
e_1_2_5_11_1
e_1_2_5_7_1
e_1_2_5_10_1
e_1_2_5_6_1
e_1_2_5_13_1
e_1_2_5_5_1
e_1_2_5_12_1
e_1_2_5_4_1
e_1_2_5_3_1
e_1_2_5_2_1
Gupta AK (e_1_2_5_8_1) 2021; 26
References_xml – volume: 161
  start-page: 791
  issue: 4
  year: 2009
  end-page: 796
  article-title: Evaluation of a polymerase chain reaction‐restriction fragment length polymorphism assay for dermatophyte and nondermatophyte identification in onychomycosis
  publication-title: Br J Dermatol
– volume: 48
  start-page: 1005
  issue: 7
  year: 2010
  end-page: 1008
  article-title: Comparison of a new commercial test, dermatophyte‐PCR kit, with conventional methods for rapid detection and identification of trichophyton rubrum in nail specimens
  publication-title: Med Mycol
– volume: 66
  start-page: 494
  issue: 3
  year: 2012
  end-page: 502
  article-title: Systematic review of nondermatophyte mold onychomycosis: Diagnosis, clinical types, epidemiology, and treatment
  publication-title: J Am Acad Dermatol
– volume: 15
  issue: 9
  year: 2020
  article-title: High prevalence of mixed infections in global onychomycosis
  publication-title: PLoS One
– volume: 39
  start-page: 2115
  issue: 6
  year: 2001
  end-page: 2121
  article-title: Utility of inoculum counting (Walshe and English criteria) in clinical diagnosis of onychomycosis caused by nondermatophytic filamentous fungi
  publication-title: J Clin Microbiol
– volume: 26
  start-page: 5
  issue: 1
  year: 2021
  end-page: 10
  article-title: Long‐term efficacy and safety of once‐daily topical efinaconazole 10% topical solution (Jublia) for dermatophyte toenail onychomycosis: An interim analysis
  publication-title: Skin Ther Lett
– volume: 1
  start-page: CD012093
  year: 2020
  article-title: Topical and device‐based treatments for fungal infections of the toenails
  publication-title: Cochrane Database Syst Rev
– volume: 170
  start-page: 182
  issue: 1
  year: 2014
  end-page: 187
  article-title: A second look at efficacy criteria for onychomycosis: Clinical and mycological cure
  publication-title: Br J Dermatol
– volume: 160
  start-page: 37
  issue: 1
  year: 2009
  end-page: 39
  article-title: New criteria for the laboratory diagnosis of nondermatophyte moulds in onychomycosis
  publication-title: Br J Dermatol
– volume: 161
  start-page: 1038
  issue: 5
  year: 2009
  end-page: 1044
  article-title: Molecular detection of dermatophytes and nondermatophytes in onychomycosis by nested polymerase chain reaction based on 28S ribosomal RNA gene sequences
  publication-title: Br J Dermatol
– volume: 107
  start-page: 280
  issue: 4
  year: 2017
  end-page: 286
  article-title: Onychomycosis infections: do polymerase chain reaction and culture reports agree?
  publication-title: J Am Podiatr Med Assoc
– volume: 39
  start-page: 685
  issue: 2
  year: 2001
  end-page: 690
  article-title: Rapid discrimination among dermatophytes, spp., and other fungi with a PCR‐restriction fragment length polymorphism ribotyping method
  publication-title: J Clin Microbiol
– volume: 37
  start-page: 931
  issue: 4
  year: 1999
  end-page: 936
  article-title: Species identification and strain differentiation of dermatophyte fungi by analysis of ribosomal‐DNA intergenic spacer regions
  publication-title: J Clin Microbiol
– volume: 36
  start-page: 202
  issue: 4
  year: 2009
  end-page: 208
  article-title: Comparative study of direct polymerase chain reaction, microscopic examination and culture‐based morphological methods for detection and identification of dermatophytes in nail and skin samples
  publication-title: J Dermatol
– volume: 5
  year: 2017
  article-title: Sensitivity, specificity, and predictive values: foundations, pliabilities, and pitfalls in research and practice
  publication-title: Front Public Health
– volume: 54
  start-page: 105
  issue: 2
  year: 2013
  end-page: 108
  article-title: Complementary role of a polymerase chain reaction test in the diagnosis of onychomycosis
  publication-title: Australas J Dermatol
– ident: e_1_2_5_7_1
  doi: 10.1111/bjd.12594
– ident: e_1_2_5_9_1
  doi: 10.1016/j.jaad.2011.02.038
– ident: e_1_2_5_4_1
  doi: 10.3109/13693781003743130
– ident: e_1_2_5_5_1
  doi: 10.1111/ajd.12027
– ident: e_1_2_5_10_1
  doi: 10.1128/JCM.39.6.2115-2121.2001
– ident: e_1_2_5_6_1
– ident: e_1_2_5_14_1
  doi: 10.1128/JCM.39.2.685-690.2001
– ident: e_1_2_5_12_1
  doi: 10.1128/JCM.37.4.931-936.1999
– ident: e_1_2_5_2_1
  doi: 10.7547/15-136
– volume: 26
  start-page: 5
  issue: 1
  year: 2021
  ident: e_1_2_5_8_1
  article-title: Long‐term efficacy and safety of once‐daily topical efinaconazole 10% topical solution (Jublia) for dermatophyte toenail onychomycosis: An interim analysis
  publication-title: Skin Ther Lett
– ident: e_1_2_5_13_1
  doi: 10.1111/j.1365-2133.2009.09291.x
– ident: e_1_2_5_3_1
  doi: 10.1111/j.1346-8138.2009.00624.x
– ident: e_1_2_5_11_1
  doi: 10.1111/j.1365-2133.2008.08805.x
– ident: e_1_2_5_17_1
  doi: 10.3389/fpubh.2017.00307
– volume: 1
  start-page: CD012093
  year: 2020
  ident: e_1_2_5_18_1
  article-title: Topical and device‐based treatments for fungal infections of the toenails
  publication-title: Cochrane Database Syst Rev
– ident: e_1_2_5_15_1
  doi: 10.1111/j.1365-2133.2009.09249.x
– ident: e_1_2_5_16_1
  doi: 10.1371/journal.pone.0239648
SSID ssj0013214
Score 2.406752
Snippet Background Increased detection of fungi including non‐dermatophyte molds (NDMs) using polymerase chain reaction (PCR) methods is well‐established. However, the...
BackgroundIncreased detection of fungi including non‐dermatophyte molds (NDMs) using polymerase chain reaction (PCR) methods is well‐established. However, the...
Increased detection of fungi including non-dermatophyte molds (NDMs) using polymerase chain reaction (PCR) methods is well-established. However, the use of PCR...
SourceID proquest
crossref
wiley
SourceType Aggregation Database
Enrichment Source
Index Database
Publisher
StartPage 1385
SubjectTerms Diagnostic systems
Evaluation
Microorganisms
Onychomycosis
Polymerase chain reaction
Visual observation
Title Utility of polymerase chain reaction for assessment of onychomycosis during topical therapy
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fijd.16241
https://www.proquest.com/docview/2724702522
https://www.proquest.com/docview/2661955340
Volume 61
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1LS8QwEA7iQbz4FtcXUTx46VLTNO3iSXyggh7EBUGh5FVcH-1iu4f11zuTPlxFQby1dErTZCb5JjPzhZA9YyXzrdUeM6n0OAh50pfcEzqKBVchqARGdK-uxXmfX96Fd1PksKmFqfgh2g03tAw3X6OBS1VMGPngyXQPBHNF65irhYDohk1EECpeb9wC7AGGqFmFMIunffPrWvQJMCdhqltnzubJQ9PCKr3kuTsqVVe_fyNv_OcvLJC5Gn_So0phFsmUzZbIzFUdYV8m9_0Ss2XHNE_pMH8Z455VYal-lIOMAsB0ZRAUkC6VLacnyuYZTqSvY50Xg4JWxY-0zIeoA7Qq8hqvkP7Z6e3xuVcfwOBpZBrzuFZBHPOeDH1hLNcpoCktlPKFDcCOU5MKFim_h6T0KhBRFACY0Mw33MKdjYNVMp3lmV0jVClmDLMSHErLQ6kAJjETyNiEkRbgpXbIfjMUia7ZyfGQjJek8VKgsxLXWR2y24oOK0qOn4Q2m_FMaqssEhYxHgHIY6xDdtrHYE8YJJGZzUcgA4ClF4YB96FJbvB-_0hycXniLtb_LrpBZhlWULhyxk0yXb6N7BbgmlJtOwX-AGj29EE
linkProvider Wiley-Blackwell
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3dS9xAEB9Eofal2triVW23xQdfcqSbzSYHfSlaOT_OB_FAkBL2K_SsTQ4v93D-9c5sPryWFkrfEjIhm92Z3d_M7PwWYN86xUPnTMBtrgKBQoEKlQikSVIpdIwqQRnd0YUcjsXpdXy9Ap_bWpiaH6ILuJFl-PmaDJwC0ktWPrm1_U-SU9X6Gp3o7R2qS76UQ6iZvSkIOEAU0fAK0T6e7tVfV6MniLkMVP1Kc7wB39o21htMfvTnle6bh9_oG__3JzbhRQNB2ZdaZ17CiitewbNRk2TfgptxRRtmF6zM2bS8W1DYauaY-a4mBUOM6SshGIJdpjpaT5ItC5pLfy5MOZvMWF3_yKpySmrA6jqvxWsYH3-9OhwGzRkMgSGysUAYHaWpGKg4lNYJkyOgMlLrULoITTm3ueSJDgfES68jmSQR4gnDQysc3rk0egOrRVm4bWBac2u5U-hTOhErjUiJ20ilNk6MREe1BwftWGSmISinczLustZRwc7KfGf14GMnOq1ZOf4ktNsOaNYY5izjCRcJ4jzOe_Che4wmRXkSVbhyjjKIWQZxHIkQm-RH7-8fyU5Oj_zF238XfQ_rw6vReXZ-cnG2A885FVT46sZdWK3u524PYU6l33ltfgSoyvhc
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3fb9MwED5NQ6p4YWyA6FY2g3jgJVVwHCcVT4hSbR2tEKJSJZAi_4oo25JqTR_KX89dftFNm4T2ligXxbHv7M8-f58B3lqnuO-c8bhNlSfQyFO-Ep40USyFDtElKKM7mcrTmRjPw_kOfGi4MJU-RLvgRpFR9tcU4EubbgX54rftv5ecSOuPhPRjcunhN76VQqiEvWkNcIAgopYVom087as3B6N_CHMbp5YDzWgPfjZFrPaXXPTXhe6bP7fUGx_4D0_hSQ1A2cfKY_Zhx2UH0JnUKfZn8GNW0HbZDctTtswvN7RotXLM_FKLjCHCLHkQDKEuU62oJ9nmGfWkVxuTrxYrVrEfWZEvyQlYxfLaPIfZ6PP3T6defQKDZ0hqzBNGB3EsBir0pXXCpAinjNTaly7AQE5tKnmk_QGp0utARlGAaMJw3wqHdy4OXsBulmfuJTCtubXcKZxROhEqjTiJ20DFNoyMxGlqF941TZGYWp6cTsm4TJppClZWUlZWF960pstKk-Muo17TnkkdlquER1xEiPI478Lr9jEGFGVJVObyNdogYhmEYSB8LFLZePd_JDkbD8uLw_83PYHO1-Eo-XI2PT-Cx5zYFCW1sQe7xfXavUKMU-jj0pf_AuSf9xQ
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Utility+of+polymerase+chain+reaction+for+assessment+of+onychomycosis+during+topical+therapy&rft.jtitle=International+journal+of+dermatology&rft.au=Gupta%2C+Aditya+K&rft.au=Cooper%2C+Elizabeth+A&rft.au=Summerbell%2C+Richard+C&rft.au=Nakrieko%2C+Kerry-Ann&rft.date=2022-11-01&rft.issn=1365-4632&rft.eissn=1365-4632&rft.volume=61&rft.issue=11&rft.spage=1385&rft_id=info:doi/10.1111%2Fijd.16241&rft.externalDBID=NO_FULL_TEXT
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0011-9059&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0011-9059&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0011-9059&client=summon