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Showing results (51-60 of 90) with videos related to

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Human Molecular Genetics|August 15, 2000
The Conradi-Hünermann-Happle syndrome (CDPX2) and emopamil binding protein: novel mutations, and somatic and gonadal mosaicismC Has, L Bruckner-Tuderman, D Müller, et al.
The British Journal of Dermatology|July 13, 2010
Poikiloderma with neutropenia: a novel C16orf57 mutation and clinical diagnostic criteriaA W Arnold, P H Itin, M Pigors, et al.
Clinical and Experimental Dermatology|June 22, 2021
HPV-5-associated cutaneous squamous cell carcinoma in situ in poikiloderma with neutropeniaA Kreuter, B Koushk-Jalali, B Akgül, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|March 4, 2020
Aberrant splicing as potential modifier of the phenotype of junctional epidermolysis bullosaR Mittwollen, S Wohlfart, J Park, et al.
AJNR. American Journal of Neuroradiology|November 17, 2012
Effect of patient sex on white matter alterations in unilateral medial temporal lobe epilepsy with hippocampal sclerosis assessed by diffusion tensor imagingK K Oguz, I Tezer, E Sanverdi, et al.
The British Journal of Dermatology|June 16, 2015
A COL7A1 variant leading to in-frame skipping of exon 15 attenuates disease severity in recessive dystrophic epidermolysis bullosaA Schwieger-Briel, L Weibel, N Chmel, et al.
The British Journal of Dermatology|January 3, 2013
Induction of senescence pathways in Kindler syndrome primary keratinocytesE Piccinni, G Di Zenzo, R Maurelli, et al.
The British Journal of Dermatology|February 1, 2011
Late-onset inversa recessive dystrophic epidermolysis bullosa caused by glycine substitutions in collagen type VIIM Leverkus, A Ambach, M Hoefeld-Fegeler, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|November 22, 2021
Esophageal carcinoma in severe recessive dystrophic epidermolysis bullosa-an underestimated complication?A Schwieger-Briel, L Trefzer, H Schumann, et al.
The British Journal of Dermatology|May 30, 2012
Verrucous carcinoma in epidermolysis bullosa simplex is possibly associated with a novel mutation in the keratin 5 geneH Schumann, W Roth, C Has, et al.
Pageof 9

Showing results (51-60 of 90) with videos related to

Sort By:
Pageof 9
Human Molecular Genetics|August 15, 2000
The Conradi-Hünermann-Happle syndrome (CDPX2) and emopamil binding protein: novel mutations, and somatic and gonadal mosaicismC Has, L Bruckner-Tuderman, D Müller, et al.
The British Journal of Dermatology|July 13, 2010
Poikiloderma with neutropenia: a novel C16orf57 mutation and clinical diagnostic criteriaA W Arnold, P H Itin, M Pigors, et al.
Clinical and Experimental Dermatology|June 22, 2021
HPV-5-associated cutaneous squamous cell carcinoma in situ in poikiloderma with neutropeniaA Kreuter, B Koushk-Jalali, B Akgül, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|March 4, 2020
Aberrant splicing as potential modifier of the phenotype of junctional epidermolysis bullosaR Mittwollen, S Wohlfart, J Park, et al.
AJNR. American Journal of Neuroradiology|November 17, 2012
Effect of patient sex on white matter alterations in unilateral medial temporal lobe epilepsy with hippocampal sclerosis assessed by diffusion tensor imagingK K Oguz, I Tezer, E Sanverdi, et al.
The British Journal of Dermatology|June 16, 2015
A COL7A1 variant leading to in-frame skipping of exon 15 attenuates disease severity in recessive dystrophic epidermolysis bullosaA Schwieger-Briel, L Weibel, N Chmel, et al.
The British Journal of Dermatology|January 3, 2013
Induction of senescence pathways in Kindler syndrome primary keratinocytesE Piccinni, G Di Zenzo, R Maurelli, et al.
The British Journal of Dermatology|February 1, 2011
Late-onset inversa recessive dystrophic epidermolysis bullosa caused by glycine substitutions in collagen type VIIM Leverkus, A Ambach, M Hoefeld-Fegeler, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|November 22, 2021
Esophageal carcinoma in severe recessive dystrophic epidermolysis bullosa-an underestimated complication?A Schwieger-Briel, L Trefzer, H Schumann, et al.
The British Journal of Dermatology|May 30, 2012
Verrucous carcinoma in epidermolysis bullosa simplex is possibly associated with a novel mutation in the keratin 5 geneH Schumann, W Roth, C Has, et al.
Pageof 9