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Martin Theiler

Showing results (61-70 of 67) with videos related to

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American Journal of Human Genetics|November 28, 2016
Monoallelic Mutations in the Translation Initiation Codon of KLHL24 Cause Skin FragilityYinghong He, Kristin Maier, Juna Leppert, et al.
Journal of the American Academy of Dermatology|December 6, 2020
Molecular characterization and natural history of linear porokeratosis: A case seriesMina Saleva-Stateva, Maria Hess, Kristin Technau-Hafsi, et al.
Pediatric Dermatology|August 20, 2024
Segmental congenital vascular anomaly with atrophy, ulceration, and scarring (SeCVAUS): Case series and review of literatureMarta Ivars, Ilona J Frieden, Lauren Provini, et al.
The Journal of Investigative Dermatology|August 19, 2018
Epidermolysis Bullosa Simplex with KLHL24 Mutations Is Associated with Dilated CardiomyopathyAgnes Schwieger-Briel, Ignacia Fuentes, Daniele Castiglia, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|September 29, 2019
Multidisciplinary long-term care and modern surgical treatment of congenital melanocytic nevi - recommendations by the CMN surgery networkHagen Ott, Sven Krengel, Otfrid Beck, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|October 22, 2019
Hagen Ott, Sven Krengel, Otfrid Beck, et al.
Archives of Dermatological Research|March 14, 2020
Clinical characteristics of pediatric hidradenitis suppurativa: a cross-sectional multicenter study of 140 patientsPeter Theut Riis, Ditte Marie Saunte, Viktoria Sigsgaard, et al.
Pageof 7

Showing results (61-70 of 67) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 67 results.
American Journal of Human Genetics|November 28, 2016
Monoallelic Mutations in the Translation Initiation Codon of KLHL24 Cause Skin FragilityYinghong He, Kristin Maier, Juna Leppert, et al.
Journal of the American Academy of Dermatology|December 6, 2020
Molecular characterization and natural history of linear porokeratosis: A case seriesMina Saleva-Stateva, Maria Hess, Kristin Technau-Hafsi, et al.
Pediatric Dermatology|August 20, 2024
Segmental congenital vascular anomaly with atrophy, ulceration, and scarring (SeCVAUS): Case series and review of literatureMarta Ivars, Ilona J Frieden, Lauren Provini, et al.
The Journal of Investigative Dermatology|August 19, 2018
Epidermolysis Bullosa Simplex with KLHL24 Mutations Is Associated with Dilated CardiomyopathyAgnes Schwieger-Briel, Ignacia Fuentes, Daniele Castiglia, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|September 29, 2019
Multidisciplinary long-term care and modern surgical treatment of congenital melanocytic nevi - recommendations by the CMN surgery networkHagen Ott, Sven Krengel, Otfrid Beck, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|October 22, 2019
Hagen Ott, Sven Krengel, Otfrid Beck, et al.
Archives of Dermatological Research|March 14, 2020
Clinical characteristics of pediatric hidradenitis suppurativa: a cross-sectional multicenter study of 140 patientsPeter Theut Riis, Ditte Marie Saunte, Viktoria Sigsgaard, et al.
Pageof 7