Routine laboratory test enabling the detection of dermatophytes and the identification of Trichophyton rubrum by means of in-house duplex real-time PCR.

[1]  S. Coloe.  Epidermophyton , 2020, Definitions.

[2]  K. Makimura,et al.  Assessment of a pan‐dermatophyte nested‐PCR compared with conventional methods for direct detection and identification of dermatophytosis agents in animals , 2018, Mycoses.

[3]  A. Nasiri,et al.  Specific Identification and Antifungal Susceptibility Pattern of Clinically Important Dermatophyte Species Isolated from Patients with Dermatophytosis in Tehran, Iran , 2018, Archives of Clinical Infectious Diseases.

[4]  B. Yakubu,et al.  Molecular characterization of dermatophytes isolated from cattle in Plateau State, Nigeria. , 2018, Veterinary microbiology.

[5]  Mahadevan Kumar,et al.  Evaluation of three DNA extraction methods from fungal cultures. , 2017, Medical journal, Armed Forces India.

[6]  J. Sherchand,et al.  Clinicomycological Characterization of Superficial Mycoses from a Tertiary Care Hospital in Nepal , 2016, Dermatology research and practice.

[7]  S. Y. Park,et al.  PCR–reverse blot hybridization assay for fast and accurate identification of causative species in superficial fungal infections , 2016, Clinical and experimental dermatology.

[8]  C. Kupsch,et al.  Detection of common dermatophytes in clinical specimens using a simple quantitative real‐time TaqMan polymerase chain reaction assay , 2016, The British journal of dermatology.

[9]  Z. Wan,et al.  Development and Evaluation of a Novel Real-Time PCR for Pan-Dermatophyte Detection in Nail Specimens , 2015, Mycopathologia.

[10]  A. Brillowska-Dąbrowska,et al.  Real-time PCR approach in dermatophyte detection and Trichophyton rubrum identification. , 2015, Acta biochimica Polonica.

[11]  A. Romanelli,et al.  A universal DNA extraction and PCR amplification method for fungal rDNA sequence‐based identification , 2014, Mycoses.

[12]  M. Feuilhade de Chauvin.  [Treatment of onychomycosis]. , 2014, Journal de mycologie medicale.

[13]  S. Ranque,et al.  Comparison of real-time PCR with conventional methods to detect dermatophytes in samples from patients with suspected dermatophytosis. , 2013, Journal of microbiological methods.

[14]  N. Kondori,et al.  Comparison of Dermatophyte PCR Kit with Conventional Methods for Detection of Dermatophytes in Skin Specimens , 2013, Mycopathologia.

[15]  M. Eshraghian,et al.  Use of Single-enzyme PCR-restriction Digestion Barcode Targeting the Internal Transcribed Spacers (ITS rDNA) to Identify Dermatophyte Species , 2012, Iranian journal of public health.

[16]  A. Kooistra-Smid,et al.  Trapped in keratin; a comparison of dermatophyte detection in nail, skin and hair samples directly from clinical samples using culture and real-time PCR. , 2011, Journal of microbiological methods.

[17]  Henrik Stryhn,et al.  Selection of a Cutoff Value for Real-Time Polymerase Chain Reaction Results to Fit a Diagnostic Purpose: Analytical and Epidemiologic Approaches , 2011, Journal of veterinary diagnostic investigation : official publication of the American Association of Veterinary Laboratory Diagnosticians, Inc.

[18]  L. Schouls,et al.  Validation of PCR-reverse line blot, a method for rapid detection and identification of nine dermatophyte species in nail, skin and hair samples. , 2008, Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases.

[19]  J. Bouchara,et al.  Updates on the Epidemiology of Dermatophyte Infections , 2008, Mycopathologia.

[20]  J. McKerrow,et al.  Purification and characterization of a 27,000-Mr extracellular proteinase from Trichophyton rubrum , 1989, Infection and immunity.