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Liat Samuelov

Showing results (31-40 of 61) with videos related to

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International Journal of Dermatology|June 27, 2025
Expanding the Phenotypic Spectrum of PIK3CA-Related DisordersJanan Mohamad, Ofer Sarig, Mor Pavlovsky, 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.
Pediatric Dermatology|March 1, 2018
Risk of intraocular and other extracutaneous involvement in patients with cutaneous juvenile xanthogranulomaLiat Samuelov, Michael Kinori, Sarah L Chamlin, 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.
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.
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.
The British Journal of Dermatology|July 13, 2022
Heterozygous variants in the integrin subunit beta 4 gene (ITGB4) cause autosomal dominant nail dystrophyKiril Malovitski, Odile Meijers, Eran Cohen-Barak, et al.
Pageof 7

Showing results (31-40 of 61) with videos related to

Sort By:
Pageof 7
International Journal of Dermatology|June 27, 2025
Expanding the Phenotypic Spectrum of PIK3CA-Related DisordersJanan Mohamad, Ofer Sarig, Mor Pavlovsky, 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.
Pediatric Dermatology|March 1, 2018
Risk of intraocular and other extracutaneous involvement in patients with cutaneous juvenile xanthogranulomaLiat Samuelov, Michael Kinori, Sarah L Chamlin, 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.
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.
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.
The British Journal of Dermatology|July 13, 2022
Heterozygous variants in the integrin subunit beta 4 gene (ITGB4) cause autosomal dominant nail dystrophyKiril Malovitski, Odile Meijers, Eran Cohen-Barak, et al.
Pageof 7