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O Sarig

Showing results (1-10 of 35) with videos related to

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The British Journal of Dermatology|February 22, 2011
An exceptional mutational event leading to Chanarin-Dorfman syndrome in a large consanguineous familyL Samuelov, D Fuchs-Telem, O Sarig, et al.
The British Journal of Dermatology|January 4, 2020
Treatment of epidermolysis bullosa pruriginosa-associated pruritus with dupilumabW Shehadeh, O Sarig, J Bar, et al.
Clinical and Experimental Dermatology|February 18, 2021
Atypical presentation of laryngo-onycho-cutaneous syndrome resulting from novel mutations in LAMA3AD Vodo, N Malchin, A DeRowe, et al.
Clinical and Experimental Dermatology|October 11, 2011
Beneficial effect of acitretin in Chanarin-Dorfman syndromeS Israeli, Y Pessach, O Sarig, et al.
Clinical and Experimental Dermatology|February 13, 2013
Epidermolytic palmoplantar keratoderma caused by activation of a cryptic splice site in KRT9D Fuchs-Telem, G Padalon-Brauch, O Sarig, et al.
Harefuah|April 17, 2003
[Sepsis, disseminated intravascular coagulation (DIC) and hematological aspects as an unusual manifestation of congenital syphilis]O Sarig, J Amir, H Tamary, et al.
The British Journal of Dermatology|June 27, 2018
Identification of a recurrent mutation in ATP2C1 demonstrates that papular acantholytic dyskeratosis and Hailey-Hailey disease are allelic disordersD Vodo, N Malchin, M Furman, et al.
Clinical and Experimental Dermatology|July 28, 2011
Molecular evidence for the role of X-chromosome inactivation in linear presentation of X-linked hypohidrotic ectodermal dysplasiaM Pavlovsky, D Fuchs-Telem, J Nousbeck, et al.
The British Journal of Dermatology|December 24, 2017
Novel POFUT1 mutation associated with hidradenitis suppurativa-Dowling-Degos disease firm up a role for Notch signalling in the pathogenesis of this disorder: reply from the authorsM Pavlovsky, O Sarig, M Eskin-Schwartz, et al.
The British Journal of Dermatology|March 20, 2014
Clinical response to ustekinumab in familial pityriasis rubra pilaris caused by a novel mutation in CARD14O Eytan, O Sarig, E Sprecher, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
The British Journal of Dermatology|February 22, 2011
An exceptional mutational event leading to Chanarin-Dorfman syndrome in a large consanguineous familyL Samuelov, D Fuchs-Telem, O Sarig, et al.
The British Journal of Dermatology|January 4, 2020
Treatment of epidermolysis bullosa pruriginosa-associated pruritus with dupilumabW Shehadeh, O Sarig, J Bar, et al.
Clinical and Experimental Dermatology|February 18, 2021
Atypical presentation of laryngo-onycho-cutaneous syndrome resulting from novel mutations in LAMA3AD Vodo, N Malchin, A DeRowe, et al.
Clinical and Experimental Dermatology|October 11, 2011
Beneficial effect of acitretin in Chanarin-Dorfman syndromeS Israeli, Y Pessach, O Sarig, et al.
Clinical and Experimental Dermatology|February 13, 2013
Epidermolytic palmoplantar keratoderma caused by activation of a cryptic splice site in KRT9D Fuchs-Telem, G Padalon-Brauch, O Sarig, et al.
Harefuah|April 17, 2003
[Sepsis, disseminated intravascular coagulation (DIC) and hematological aspects as an unusual manifestation of congenital syphilis]O Sarig, J Amir, H Tamary, et al.
The British Journal of Dermatology|June 27, 2018
Identification of a recurrent mutation in ATP2C1 demonstrates that papular acantholytic dyskeratosis and Hailey-Hailey disease are allelic disordersD Vodo, N Malchin, M Furman, et al.
Clinical and Experimental Dermatology|July 28, 2011
Molecular evidence for the role of X-chromosome inactivation in linear presentation of X-linked hypohidrotic ectodermal dysplasiaM Pavlovsky, D Fuchs-Telem, J Nousbeck, et al.
The British Journal of Dermatology|December 24, 2017
Novel POFUT1 mutation associated with hidradenitis suppurativa-Dowling-Degos disease firm up a role for Notch signalling in the pathogenesis of this disorder: reply from the authorsM Pavlovsky, O Sarig, M Eskin-Schwartz, et al.
The British Journal of Dermatology|March 20, 2014
Clinical response to ustekinumab in familial pityriasis rubra pilaris caused by a novel mutation in CARD14O Eytan, O Sarig, E Sprecher, et al.
Pageof 4