Shirli Israeli
Tel Aviv, TA, Israel
Last Updated: 09/26/2026
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Found 9 publications
Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa.
Journal: Pediatric dermatology
Published: June 30, 2023
Molecular epidemiology of non-syndromic autosomal recessive congenital ichthyosis in a Middle-Eastern population.
Journal: Experimental dermatology
Published: December 29, 2020
A mutation in TP63 causing a mild ectodermal dysplasia phenotype.
Journal: The Journal of investigative dermatology
Published: March 29, 2014
Molecular analysis of a series of Israeli families with Comèl-Netherton syndrome.
Journal: Dermatology (Basel, Switzerland)
Published: July 14, 2013
Semidominant inheritance in epidermolytic ichthyosis.
Journal: The Journal of investigative dermatology
Published: April 23, 2013
The sound of silence: autosomal recessive congenital ichthyosis caused by a synonymous mutation in ABCA12.
Journal: Experimental dermatology
Published: February 07, 2013
Population-specific association between a polymorphic variant in ST18, encoding a pro-apoptotic molecule, and pemphigus vulgaris.
Journal: The Journal of investigative dermatology
Published: March 23, 2012
Familial pityriasis rubra pilaris is caused by mutations in CARD14.
Journal: American journal of human genetics
Published: February 29, 2012
Short stature, onychodysplasia, facial dysmorphism, and hypotrichosis syndrome is caused by a POC1A mutation.
Journal: American journal of human genetics
Published: February 27, 2012
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Last Updated: 09/26/2026