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Showing results (81-90 of 90) with videos related to

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The British Journal of Dermatology|March 19, 2013
Phenotypic spectrum of epidermolysis bullosa associated with α6β4 integrin mutationsH Schumann, D Kiritsi, M Pigors, et al.
Brain and Behavior|June 25, 2026
The "Brain's Traffic Map" Reveals Neural Pathways Linked to Coronary Microvascular Dysfunction in WomenArzu C Has Silemek, Jeffrey C Wertheimer, Janet Wei, et al.
The British Journal of Dermatology|May 16, 2019
Clinical practice guidelines for laboratory diagnosis of epidermolysis bullosaC Has, L Liu, M C Bolling, et al.
The British Journal of Dermatology|March 18, 2014
Under-recognition of acral peeling skin syndrome: 59 new cases with 15 novel mutationsW Szczecinska, D Nesteruk, K Wertheim-Tysarowska, et al.
The British Journal of Dermatology|January 18, 2017
Sixteen novel mutations in PNPLA1 in patients with autosomal recessive congenital ichthyosis reveal the importance of an extended patatin domain in PNPLA1 that is essential for proper human skin barrier functionA D Zimmer, G-J Kim, A Hotz, et al.
Multiple Sclerosis and Related Disorders|April 9, 2026
Twelve-week intermittent hypoxia intervention in multiple sclerosis - A safety and feasibility trialCharlotte Schubert, Anna Suling, Caren Ramien, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|December 14, 2024
Oral health care pathways for patients with epidermolysis bullosa: A position statement from the European reference network for rare skin diseasesS Krämer, A L Hillebrecht, K Bekes, et al.
Annals of Clinical and Translational Neurology|March 17, 2026
Paramagnetic Rim Lesions Are Associated With Trans-Synaptic Degeneration of the Visual Pathway in Multiple SclerosisAbdul Jaber Tayem, Angel Liu, Sargis Manukyan, et al.
The British Journal of Dermatology|February 5, 2020
Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragilityC Has, J W Bauer, C Bodemer, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|March 3, 2022
Proposal for a 6-step approach for differential diagnosis of neonatal erythrodermaE Cuperus, A Bygum, L Boeckmann, et al.
Pageof 9

Showing results (81-90 of 90) with videos related to

Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 90 results.
The British Journal of Dermatology|March 19, 2013
Phenotypic spectrum of epidermolysis bullosa associated with α6β4 integrin mutationsH Schumann, D Kiritsi, M Pigors, et al.
Brain and Behavior|June 25, 2026
The "Brain's Traffic Map" Reveals Neural Pathways Linked to Coronary Microvascular Dysfunction in WomenArzu C Has Silemek, Jeffrey C Wertheimer, Janet Wei, et al.
The British Journal of Dermatology|May 16, 2019
Clinical practice guidelines for laboratory diagnosis of epidermolysis bullosaC Has, L Liu, M C Bolling, et al.
The British Journal of Dermatology|March 18, 2014
Under-recognition of acral peeling skin syndrome: 59 new cases with 15 novel mutationsW Szczecinska, D Nesteruk, K Wertheim-Tysarowska, et al.
The British Journal of Dermatology|January 18, 2017
Sixteen novel mutations in PNPLA1 in patients with autosomal recessive congenital ichthyosis reveal the importance of an extended patatin domain in PNPLA1 that is essential for proper human skin barrier functionA D Zimmer, G-J Kim, A Hotz, et al.
Multiple Sclerosis and Related Disorders|April 9, 2026
Twelve-week intermittent hypoxia intervention in multiple sclerosis - A safety and feasibility trialCharlotte Schubert, Anna Suling, Caren Ramien, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|December 14, 2024
Oral health care pathways for patients with epidermolysis bullosa: A position statement from the European reference network for rare skin diseasesS Krämer, A L Hillebrecht, K Bekes, et al.
Annals of Clinical and Translational Neurology|March 17, 2026
Paramagnetic Rim Lesions Are Associated With Trans-Synaptic Degeneration of the Visual Pathway in Multiple SclerosisAbdul Jaber Tayem, Angel Liu, Sargis Manukyan, et al.
The British Journal of Dermatology|February 5, 2020
Consensus reclassification of inherited epidermolysis bullosa and other disorders with skin fragilityC Has, J W Bauer, C Bodemer, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|March 3, 2022
Proposal for a 6-step approach for differential diagnosis of neonatal erythrodermaE Cuperus, A Bygum, L Boeckmann, et al.
Pageof 9