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E Sprecher

Showing results (121-130 of 200) with videos related to

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Clinical and Experimental Dermatology|March 19, 2014
New intragenic and promoter region deletion mutations in FERMT1 underscore genetic homogeneity in Kindler syndromeD Fuchs-Telem, J Nousbeck, A Singer, et al.
The British Journal of Dermatology|March 8, 2014
The expanding spectrum of IgA pemphigus: a case report and review of the literatureS Geller, A Gat, T Zeeli, et al.
Journal of the Neurological Sciences|June 9, 2009
Embolic potential and ultrasonic characteristics of plaques in patients with severe unilateral carotid restenosis more than one year after surgeryG Telman, E Kouperberg, A Hlebtovsky, 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.
International Journal of Impotence Research|June 1, 1996
Polyneuropathy in impotenceY Vardi, E Sprecher, Y Kanter, et al.
The British Journal of Dermatology|June 10, 2014
Mutations in SMARCAD1 cause autosomal dominant adermatoglyphia and perturb the expression of epidermal differentiation-associated genesJ Nousbeck, O Sarig, L Magal, et al.
Clinical and Experimental Dermatology|February 21, 2018
Topical pimecrolimus for paediatric cutaneous mastocytosisJ Mashiah, A Harel, C Bodemer, et al.
Clinical and Experimental Dermatology|February 23, 2019
Efficacy of a combination of diluted calcium hydroxylapatite-based filler and an energy-based device for the treatment of facial atrophic acne scarsA Koren, G Isman, S Cohen, et al.
Clinical and Experimental Dermatology|May 10, 2006
A homozygous missense mutation in PEPD encoding peptidase D causes prolidase deficiency associated with hyper-IgE syndromeT Hershkovitz, G Hassoun, M Indelman, et al.
Clinical and Experimental Dermatology|March 17, 2012
A 60-year-old woman with subcutaneous nodules on the thighM Sagi, B S Marcus, A Gat, et al.
Pageof 20

Showing results (121-130 of 200) with videos related to

Sort By:
Pageof 20
Clinical and Experimental Dermatology|March 19, 2014
New intragenic and promoter region deletion mutations in FERMT1 underscore genetic homogeneity in Kindler syndromeD Fuchs-Telem, J Nousbeck, A Singer, et al.
The British Journal of Dermatology|March 8, 2014
The expanding spectrum of IgA pemphigus: a case report and review of the literatureS Geller, A Gat, T Zeeli, et al.
Journal of the Neurological Sciences|June 9, 2009
Embolic potential and ultrasonic characteristics of plaques in patients with severe unilateral carotid restenosis more than one year after surgeryG Telman, E Kouperberg, A Hlebtovsky, 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.
International Journal of Impotence Research|June 1, 1996
Polyneuropathy in impotenceY Vardi, E Sprecher, Y Kanter, et al.
The British Journal of Dermatology|June 10, 2014
Mutations in SMARCAD1 cause autosomal dominant adermatoglyphia and perturb the expression of epidermal differentiation-associated genesJ Nousbeck, O Sarig, L Magal, et al.
Clinical and Experimental Dermatology|February 21, 2018
Topical pimecrolimus for paediatric cutaneous mastocytosisJ Mashiah, A Harel, C Bodemer, et al.
Clinical and Experimental Dermatology|February 23, 2019
Efficacy of a combination of diluted calcium hydroxylapatite-based filler and an energy-based device for the treatment of facial atrophic acne scarsA Koren, G Isman, S Cohen, et al.
Clinical and Experimental Dermatology|May 10, 2006
A homozygous missense mutation in PEPD encoding peptidase D causes prolidase deficiency associated with hyper-IgE syndromeT Hershkovitz, G Hassoun, M Indelman, et al.
Clinical and Experimental Dermatology|March 17, 2012
A 60-year-old woman with subcutaneous nodules on the thighM Sagi, B S Marcus, A Gat, et al.
Pageof 20