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Showing results (41-50 of 90) with videos related to

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The British Journal of Dermatology|January 17, 2007
Incontinentia pigmenti in a newborn with a novel nonsense mutation in the NEMO geneC Has, S Danescu, A Volz, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|November 1, 2006
[Hereditary photodermatoses]P Poblete-Gutiérrez, W H C Burgdorf, C Has, et al.
Dermatology (Basel, Switzerland)|October 13, 2010
Mild clinical phenotype of Kindler syndrome associated with late diagnosis and skin cancerC Has, B Burger, A Volz, et al.
The British Journal of Dermatology|April 14, 2015
A childhood subepidermal autoimmune bullous disease resembling mechanobullous epidermolysis bullosa acquisitaP Agrawal, R George, M Thomas, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|September 16, 2016
Compound heterozygosity for dominant and recessive DSG1 mutations in a patient with atypical SAM syndrome (severe dermatitis, multiple allergies, metabolic wasting)S Dănescu, J Leppert, R Cosgarea, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|May 7, 2021
Plantar involvement correlates with obesity, pain and impaired mobility in epidermolysis bullosa simplex: a retrospective cohort studyA Reimer-Taschenbrecker, M Hess, A Hotz, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|June 20, 2020
Lack of effect of topical statins in linear porokeratosisM Saleva-Stateva, L Weibel, M Theiler, et al.
The British Journal of Dermatology|July 10, 2013
A case of junctional epidermolysis bullosa with prurigo-like lesions and reduction of collagen XVII and filaggrinL Cifuentes, D Kiritsi, W Chen, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|November 29, 2019
An unusual type of telangiectatic naevus with underlying and surrounding dilated veins: report of four casesR Happle, D van Gysel, R Fölster-Holst, et al.
Dermatology (Basel, Switzerland)|June 23, 2012
Acromelanosis albo-punctata: a distinct inherited dermatosis with acral spotty dyspigmentation without systemic involvementA W Arnold, J S Kern, P H Itin, et al.
Pageof 9

Showing results (41-50 of 90) with videos related to

Sort By:
Pageof 9
The British Journal of Dermatology|January 17, 2007
Incontinentia pigmenti in a newborn with a novel nonsense mutation in the NEMO geneC Has, S Danescu, A Volz, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete|November 1, 2006
[Hereditary photodermatoses]P Poblete-Gutiérrez, W H C Burgdorf, C Has, et al.
Dermatology (Basel, Switzerland)|October 13, 2010
Mild clinical phenotype of Kindler syndrome associated with late diagnosis and skin cancerC Has, B Burger, A Volz, et al.
The British Journal of Dermatology|April 14, 2015
A childhood subepidermal autoimmune bullous disease resembling mechanobullous epidermolysis bullosa acquisitaP Agrawal, R George, M Thomas, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|September 16, 2016
Compound heterozygosity for dominant and recessive DSG1 mutations in a patient with atypical SAM syndrome (severe dermatitis, multiple allergies, metabolic wasting)S Dănescu, J Leppert, R Cosgarea, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|May 7, 2021
Plantar involvement correlates with obesity, pain and impaired mobility in epidermolysis bullosa simplex: a retrospective cohort studyA Reimer-Taschenbrecker, M Hess, A Hotz, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|June 20, 2020
Lack of effect of topical statins in linear porokeratosisM Saleva-Stateva, L Weibel, M Theiler, et al.
The British Journal of Dermatology|July 10, 2013
A case of junctional epidermolysis bullosa with prurigo-like lesions and reduction of collagen XVII and filaggrinL Cifuentes, D Kiritsi, W Chen, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|November 29, 2019
An unusual type of telangiectatic naevus with underlying and surrounding dilated veins: report of four casesR Happle, D van Gysel, R Fölster-Holst, et al.
Dermatology (Basel, Switzerland)|June 23, 2012
Acromelanosis albo-punctata: a distinct inherited dermatosis with acral spotty dyspigmentation without systemic involvementA W Arnold, J S Kern, P H Itin, et al.
Pageof 9