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Alexa Kassels

Showing results (11-20 of 15) with videos related to

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JAAD Case Reports|December 9, 2025
Flagellate erythema-like persistent eruption of Still's disease treated with a Janus kinase inhibitorAlexa Kassels, Christine T Pham, Deborah Moon, et al.
Journal of the American Academy of Dermatology|May 1, 2024
Response to Arbache et al., "Comment on 'Vulvar lichen sclerosus and vitiligo: Overlap and clinical features'"Susie Suh, Alexa Kassels, Kathryn Hinchee Rodriquez, et al.
International Journal of Women'S Dermatology|April 19, 2024
Use of systemic therapies for vulvar lichen sclerosus and vulvovaginal lichen planus: a survey study of dermatologists and gynecologistsCeleste Richardson, Alexa Kassels, Ashley Elsensohn, et al.
Ophthalmic Genetics|March 22, 2022
Confirmation of association of <i>TGFBI</i> p.Ser591Phe mutation with variant lattice corneal dystrophyCharlene H Choo, Doug D Chung, Kaitlyn V Ledwitch, et al.
Case Reports in Ophthalmology|April 21, 2020
Identification of a Novel Missense <i>KRT12</i> Mutation in a Vietnamese Family with Meesmann Corneal DystrophyPham Ngoc Dong, Le Xuan Cung, Tran Khanh Sam, et al.
Pageof 2

Showing results (11-20 of 15) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 15 results.
JAAD Case Reports|December 9, 2025
Flagellate erythema-like persistent eruption of Still's disease treated with a Janus kinase inhibitorAlexa Kassels, Christine T Pham, Deborah Moon, et al.
Journal of the American Academy of Dermatology|May 1, 2024
Response to Arbache et al., "Comment on 'Vulvar lichen sclerosus and vitiligo: Overlap and clinical features'"Susie Suh, Alexa Kassels, Kathryn Hinchee Rodriquez, et al.
International Journal of Women'S Dermatology|April 19, 2024
Use of systemic therapies for vulvar lichen sclerosus and vulvovaginal lichen planus: a survey study of dermatologists and gynecologistsCeleste Richardson, Alexa Kassels, Ashley Elsensohn, et al.
Ophthalmic Genetics|March 22, 2022
Confirmation of association of <i>TGFBI</i> p.Ser591Phe mutation with variant lattice corneal dystrophyCharlene H Choo, Doug D Chung, Kaitlyn V Ledwitch, et al.
Case Reports in Ophthalmology|April 21, 2020
Identification of a Novel Missense <i>KRT12</i> Mutation in a Vietnamese Family with Meesmann Corneal DystrophyPham Ngoc Dong, Le Xuan Cung, Tran Khanh Sam, et al.
Pageof 2