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Experimental Dermatology|April 1, 2018
SAM syndrome is characterized by extensive phenotypic heterogeneityShahar Taiber, Liat Samuelov, Janan Mohamad, et al.The British Journal of Dermatology|July 13, 2022
A unique skin phenotype resulting from a large heterozygous deletion spanning six keratin genesJanan Mohamad, Ofer Sarig, Paula Beattie, et al.The Journal of Investigative Dermatology|January 22, 2013
Topobiology of human pigmentation: P-cadherin selectively stimulates hair follicle melanogenesisLiat Samuelov, Eli Sprecher, Koji Sugawara, et al.American Journal of Medical Genetics. Part A|August 3, 2022
Autosomal recessive congenital ichthyosis caused by a pathogenic missense variant in CLDN1Janan Mohamad, Liat Samuelov, Sari Assaf, et al.Skin Health and Disease|December 4, 2023
SNG100, a novel topical treatment for moderate atopic dermatitis, in patients aged 6 years or older: A randomised, double-blind, active-controlled trialLiat Samuelov, Avner Shemer, Shoshana Greenberger, et al.Experimental Dermatology|November 17, 2021
Vorinostat, a histone deacetylase inhibitor, as a potential novel treatment for psoriasisLiat Samuelov, Ron Bochner, Lee Magal, et al.Immunity, Inflammation and Disease|December 21, 2021
Clinical efficacy of fecal microbial transplantation treatment in adults with moderate-to-severe atopic dermatitisJacob Mashiah, Tal Karady, Naomi Fliss-Isakov, et al.The British Journal of Dermatology|May 24, 2022
Coexistence of pachyonychia congenita and hidradenitis suppurativa: more than a coincidenceMor Pavlovsky, Alon Peled, Ofer Sarig, et al.Clinical and Experimental Dermatology|March 27, 2022
Superimposed type 2 segmental atopic dermatitis: case series and review of the literatureEfrat Bar-Ilan, Jacob Mashiah, Ronen Alkalay, et al.Current Rheumatology Reports|May 29, 2007
Tumoral calcinosis: new insights for the rheumatologist into a familial crystal deposition diseaseEli SprecherPageof 28