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C Has

Showing results (21-30 of 90) with videos related to

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Journal of the European Academy of Dermatology and Venereology : JEADV|April 14, 2015
A novel mutation in the FERMT1 gene in Turkish siblings with Kindler syndromeD Kartal, M Borlu, C Has, et al.
Case Reports in Dermatology|September 11, 2013
Acral peeling skin syndrome resembling epidermolysis bullosa simplex in a 10-month-old boyS Kavaklieva, I Yordanova, L Bruckner-Tuderman, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|December 2, 2017
Acral lamellar Ichthyosis - expanding the phenotype of temperature-sensitive keratinization disordersH de Almeida, C Has, J Fischer, et al.
The British Journal of Dermatology|June 21, 2008
Dystrophic epidermolysis bullosa pruriginosa is not associated with frequent FLG gene mutationsH Schumann, C Has, J Kohlhase, et al.
The British Journal of Dermatology|January 11, 2012
Conradi-Hünermann-Happle syndrome in males vs. MEND syndrome (male EBP disorder with neurological defects)A W Arnold, L Bruckner-Tuderman, C Has, et al.
Communications Biology|November 9, 2024
The brain's first "traffic map" through Unified Structural and Functional Connectivity (USFC) modelingArzu C Has Silemek, Haitao Chen, Pascal Sati, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|September 10, 2014
Epidemiology of inherited epidermolysis bullosa in Romania and genotype-phenotype correlations in patients with dystrophic epidermolysis bullosaS Dănescu, C Has, S Senila, et al.
The British Journal of Dermatology|July 7, 2019
Skin fragility caused by biallelic KRT10 mutations: an intriguing form of self-improving epidermolytic ichthyosisL Frommherz, J Küsel, A Zimmer, et al.
The British Journal of Dermatology|April 26, 2019
Postzygotic HRAS mutation in heterochromia of straight scalp hairC Has, R Happle, J Fischer, et al.
The British Journal of Dermatology|June 7, 2014
'Double trouble': diagnostic challenges in genetic skin disordersD Kiritsi, M Valari, K Mileounis, et al.
Pageof 9

Showing results (21-30 of 90) with videos related to

Sort By:
Pageof 9
Journal of the European Academy of Dermatology and Venereology : JEADV|April 14, 2015
A novel mutation in the FERMT1 gene in Turkish siblings with Kindler syndromeD Kartal, M Borlu, C Has, et al.
Case Reports in Dermatology|September 11, 2013
Acral peeling skin syndrome resembling epidermolysis bullosa simplex in a 10-month-old boyS Kavaklieva, I Yordanova, L Bruckner-Tuderman, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|December 2, 2017
Acral lamellar Ichthyosis - expanding the phenotype of temperature-sensitive keratinization disordersH de Almeida, C Has, J Fischer, et al.
The British Journal of Dermatology|June 21, 2008
Dystrophic epidermolysis bullosa pruriginosa is not associated with frequent FLG gene mutationsH Schumann, C Has, J Kohlhase, et al.
The British Journal of Dermatology|January 11, 2012
Conradi-Hünermann-Happle syndrome in males vs. MEND syndrome (male EBP disorder with neurological defects)A W Arnold, L Bruckner-Tuderman, C Has, et al.
Communications Biology|November 9, 2024
The brain's first "traffic map" through Unified Structural and Functional Connectivity (USFC) modelingArzu C Has Silemek, Haitao Chen, Pascal Sati, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|September 10, 2014
Epidemiology of inherited epidermolysis bullosa in Romania and genotype-phenotype correlations in patients with dystrophic epidermolysis bullosaS Dănescu, C Has, S Senila, et al.
The British Journal of Dermatology|July 7, 2019
Skin fragility caused by biallelic KRT10 mutations: an intriguing form of self-improving epidermolytic ichthyosisL Frommherz, J Küsel, A Zimmer, et al.
The British Journal of Dermatology|April 26, 2019
Postzygotic HRAS mutation in heterochromia of straight scalp hairC Has, R Happle, J Fischer, et al.
The British Journal of Dermatology|June 7, 2014
'Double trouble': diagnostic challenges in genetic skin disordersD Kiritsi, M Valari, K Mileounis, et al.
Pageof 9