A
Ardavan Tajdini
Researcher at Tehran University of Medical Sciences
Publications - 21
Citations - 129
Ardavan Tajdini is an academic researcher from Tehran University of Medical Sciences. The author has contributed to research in topics: Medicine & Randomized controlled trial. The author has an hindex of 6, co-authored 17 publications receiving 62 citations.
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Journal ArticleDOI
Subacute Thyroiditis in COVID-19 Patients
Saeed Sohrabpour,Farrokh Heidari,Ebrahim Karimi,Reza Ansari,Ardavan Tajdini,Firouzeh Heidari +5 more
TL;DR: This report may help physicians to identify lesser-known manifestations and complications of COVID-19 in patients with clinician manifestations and physical examination in favor of SAT.
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Species identification and in vitro antifungal susceptibility testing of Aspergillus section Nigri strains isolated from otomycosis patients
Z. Kamali Sarwestani,Seyed Jamal Hashemi,Sasan Rezaie,M. Gerami Shoar,Shahram Mahmoudi,Miad Elahi,M. Bahardoost,Ardavan Tajdini,S. Abutalebian,R. Daie Ghazvini +9 more
TL;DR: In this article, a set of black Aspergilli isolates from Otomycosis patients were identified by using the PCR-sequencing of the β-tubulin gene, and the susceptibility of isolates to three antifungal drugs, including fluconazole, clotrimazole (CLT), and nystatin (NS), were tested according to CLSI M38-A2.
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Investigation of Etiologic Agents and Clinical Presentations of Otomycosis at a Tertiary Referral Center in Tehran, Iran.
Hasti Kamali Sarwestani,Roshanak Daie Ghazvini,Seyed Jamal Hashemi,Sassan Rezaie,Mohsen Gerami Shoar,Shahram Mahmoudi,Miad Elahi,Ardavan Tajdini +7 more
TL;DR: Investigation at a tertiary referral center in Tehran, Iran revealed the high prevalence of C. glabrata and mixed infections in otomycosis patients and mycological examinations should be considered for proper treatment.
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Novel nucleotide changes in mutational analysis of mitochondrial 12SrRNA gene in patients with nonsyndromic and aminoglycoside-induced hearing loss.
Mohammad Ali Dowlati,Pupak Derakhshandeh-Peykar,Massoud Houshmand,Mohammad Farhadi,Azadeh Shojaei,Masoumeh Falah,Esmaiil Mohammadi,Ardavan Tajdini,Shima Arastoo,Javad Tavakkoly-Bazzaz +9 more
TL;DR: Mutational screening of entire 12SrRNA and tRNA ser (UCN) genes in 107 unrelated Iranian patients with amino glycoside-induced and nonsyndromic bilateral hearing loss by direct sequencing analysis method showed that m.1555A>G mutation is not important in the authors' population, but aminoglycoside exposure is a risk factor for clinical phenotype appearance of these mutations.
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MTHFR AND ApoE genetic variants association with sudden sensorineural hearing loss.
Armita Kakavand Hamidi,Nasrin Yazdani,Kimia Haj Seyedjavadi,Nakisa Zarrabi Ahrabi,Ardavan Tajdini,Keivan Aghazadeh,Mahsa M. Amoli +6 more
TL;DR: MTHFR C677T and ApoE gene variant may be associated with sudden sensorineural hearing loss in an Iranian population and showed that MTHFR rs1801133 allele frequency is significantly different between cases and controls.