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L Samuelov

Showing results (1-10 of 15) 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.
The British Journal of Dermatology|December 12, 2019
Revisiting pachyonychia congenita: a case-cohort study of 815 patientsL Samuelov, F J D Smith, C D Hansen, et al.
Clinical and Experimental Dermatology|June 11, 2013
Diffuse scalp alopecia in a middle-aged patientL Samuelov, U Arad, A Gat, et al.
The British Journal of Dermatology|December 16, 2014
Extensive lentigo simplex, linear epidermolytic naevus and epidermolytic naevus comedonicus caused by a somatic mutation in KRT10L Samuelov, O Sarig, A Gat, et al.
Clinical and Experimental Dermatology|January 19, 2019
PLACK syndrome shows remarkable phenotypic homogeneityJ Mohamad, L Samuelov, D Ben-Amitai, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|February 17, 2019
Nested case-control study investigating the diagnostic role of tissue eosinophilia in adverse cutaneous drug reactionsL Samuelov, A Nathan, E Slutsky, et al.
Clinical and Experimental Dermatology|December 27, 2017
Recessive epidermolytic ichthyosis results from loss of keratin 10 expression, regardless of the mutation locationD Vodo, O Sarig, A Peled, et al.
Clinical and Experimental Dermatology|February 24, 2015
A case for diagnosisL Samuelov, O Sarig, T Goldsmith, 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.
Pageof 2

Showing results (1-10 of 15) with videos related to

Sort By:
Pageof 2
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.
The British Journal of Dermatology|December 12, 2019
Revisiting pachyonychia congenita: a case-cohort study of 815 patientsL Samuelov, F J D Smith, C D Hansen, et al.
Clinical and Experimental Dermatology|June 11, 2013
Diffuse scalp alopecia in a middle-aged patientL Samuelov, U Arad, A Gat, et al.
The British Journal of Dermatology|December 16, 2014
Extensive lentigo simplex, linear epidermolytic naevus and epidermolytic naevus comedonicus caused by a somatic mutation in KRT10L Samuelov, O Sarig, A Gat, et al.
Clinical and Experimental Dermatology|January 19, 2019
PLACK syndrome shows remarkable phenotypic homogeneityJ Mohamad, L Samuelov, D Ben-Amitai, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|February 17, 2019
Nested case-control study investigating the diagnostic role of tissue eosinophilia in adverse cutaneous drug reactionsL Samuelov, A Nathan, E Slutsky, et al.
Clinical and Experimental Dermatology|December 27, 2017
Recessive epidermolytic ichthyosis results from loss of keratin 10 expression, regardless of the mutation locationD Vodo, O Sarig, A Peled, et al.
Clinical and Experimental Dermatology|February 24, 2015
A case for diagnosisL Samuelov, O Sarig, T Goldsmith, 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.
Pageof 2