Showing results (11-20 of 79) with videos related to
Sort By:
Pageof 8
Trends in Molecular Medicine|November 10, 2019
Applications of Spherical Nucleic Acid Nanoparticles as Delivery SystemsAhad Mokhtarzadeh, Hassan Vahidnezhad, Leila Youssefian, et al.Experimental Dermatology|March 5, 2022
Whole-transcriptome sequencing identifies postzygotic ATP2A2 mutations in a patient misdiagnosed with herpes zoster, confirming the diagnosis of very late-onset segmental Darier diseaseFatemeh Mohaghegh, Leila Youssefian, Hamid Galehdari, et al.Journal of the European Academy of Dermatology and Venereology : JEADV|September 27, 2022
Acquired ichthyosis, asteatotic dermatitis or xerosis? An update on pathoetiology and drug-induced associationsJason S Park, Amir H Saeidian, Leila Youssefian, et al.Experimental Dermatology|March 11, 2022
Pathogenic DST sequence variants result in either epidermolysis bullosa simplex (EBS) or hereditary sensory and autonomic neuropathy type 6 (HSAN-VI)Raziyeh Khalesi, Nailah Harvey, Masoud Garshasbi, et al.Molecular Genetics & Genomic Medicine|September 28, 2019
Hypotrichosis with juvenile macular dystrophy: Combination of whole-genome sequencing and genome-wide homozygosity mapping identifies a large deletion in CDH3 initially undetected by whole-exome sequencing-A lesson from next-generation sequencingAmir Hossein Saeidian, Hassan Vahidnezhad, Leila Youssefian, et al.Orphanet Journal of Rare Diseases|December 7, 2017
A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndromeLeila Youssefian, Andrew Touati, Amir Hossein Saeidian, et al.Experimental Dermatology|September 30, 2020
Increased level of cathelicidin (LL-37) in vitiligo: Possible pathway independent from vitamin D receptor gene polymorphismFatemeh Atazadeh, Zahra Fazeli, Hassan Vahidnezhad, et al.Iranian Biomedical Journal|December 1, 2009
Modeling breast acini in tissue culture for detection of malignant phenotype reversion to non-malignant phenotypeHassan Vahidnezhad, Leila Youssefian, Mahmoud Jeddi-Tehrani, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|September 30, 2016
Co-existence of phenylketonuria either with maple syrup urine disease or Sandhoff disease in two patients from Iran: emphasizing the role of consanguinityMaryam Abiri, Saeed Talebi, Jouni Uitto, et al.Experimental Dermatology|April 30, 2020
The matriptase-prostasin proteolytic cascade in dermatologic diseasesAndrew Touati, Amir Hossein Saeidian, Leila Youssefian, et al.Pageof 8