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O Sarig

Showing results (21-30 of 35) with videos related to

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The British Journal of Dermatology|January 30, 2016
Segmental basal cell naevus syndrome caused by an activating mutation in smoothenedZ Khamaysi, R Bochner, M Indelman, et al.
Clinical and Experimental Dermatology|January 24, 2021
Identification of clinically useful predictive genetic variants in pachyonychia congenitaL Samuelov, O Sarig, N Adir, et al.
The British Journal of Dermatology|November 21, 2019
Treatment of hereditary hypotrichosis simplex of the scalp with topical gentamicinA Peled, L Samuelov, O Sarig, et al.
Clinical and Experimental Dermatology|October 13, 2016
A novel homozygous deletion in EXPH5 causes a skin fragility phenotypeN Malchin, O Sarig, M Grafi-Cohen, et al.
Clinical and Experimental Dermatology|March 8, 2021
Evidence for cutaneous dysbiosis in dystrophic epidermolysis bullosaJ Bar, O Sarig, M Lotan-Pompan, et al.
The British Journal of Dermatology|November 18, 2020
ST18 affects cell-cell adhesion in pemphigus vulgaris in a tumour necrosis factor-α-dependent fashionS Assaf, L Malki, T Mayer, et al.
The British Journal of Dermatology|September 19, 2017
A phenotype combining hidradenitis suppurativa with Dowling-Degos disease caused by a founder mutation in PSENENM Pavlovsky, O Sarig, M Eskin-Schwartz, et al.
The British Journal of Dermatology|January 10, 2018
Striate palmoplantar keratoderma resulting from a missense mutation in DSG1D Vodo, E A O'Toole, N Malchin, et al.
Clinical and Experimental Dermatology|April 30, 2013
Non-syndromic autosomal recessive congenital ichthyosis in the Israeli populationS Israeli, I Goldberg, D Fuchs-Telem, et al.
The British Journal of Dermatology|April 14, 2020
Identification of a founder mutation in KRT14 associated with Naegeli-Franceschetti-Jadassohn syndromeD J Ralser, S Kumar, O Borisov, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
The British Journal of Dermatology|January 30, 2016
Segmental basal cell naevus syndrome caused by an activating mutation in smoothenedZ Khamaysi, R Bochner, M Indelman, et al.
Clinical and Experimental Dermatology|January 24, 2021
Identification of clinically useful predictive genetic variants in pachyonychia congenitaL Samuelov, O Sarig, N Adir, et al.
The British Journal of Dermatology|November 21, 2019
Treatment of hereditary hypotrichosis simplex of the scalp with topical gentamicinA Peled, L Samuelov, O Sarig, et al.
Clinical and Experimental Dermatology|October 13, 2016
A novel homozygous deletion in EXPH5 causes a skin fragility phenotypeN Malchin, O Sarig, M Grafi-Cohen, et al.
Clinical and Experimental Dermatology|March 8, 2021
Evidence for cutaneous dysbiosis in dystrophic epidermolysis bullosaJ Bar, O Sarig, M Lotan-Pompan, et al.
The British Journal of Dermatology|November 18, 2020
ST18 affects cell-cell adhesion in pemphigus vulgaris in a tumour necrosis factor-α-dependent fashionS Assaf, L Malki, T Mayer, et al.
The British Journal of Dermatology|September 19, 2017
A phenotype combining hidradenitis suppurativa with Dowling-Degos disease caused by a founder mutation in PSENENM Pavlovsky, O Sarig, M Eskin-Schwartz, et al.
The British Journal of Dermatology|January 10, 2018
Striate palmoplantar keratoderma resulting from a missense mutation in DSG1D Vodo, E A O'Toole, N Malchin, et al.
Clinical and Experimental Dermatology|April 30, 2013
Non-syndromic autosomal recessive congenital ichthyosis in the Israeli populationS Israeli, I Goldberg, D Fuchs-Telem, et al.
The British Journal of Dermatology|April 14, 2020
Identification of a founder mutation in KRT14 associated with Naegeli-Franceschetti-Jadassohn syndromeD J Ralser, S Kumar, O Borisov, et al.
Pageof 4