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Keith Choate

Showing results (11-20 of 38) with videos related to

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JAMA Dermatology|August 1, 2019
Association of the Severity of Alopecia With the Severity of IchthyosisElana Putterman, Theodore Zaki, Leonard Milstone, et al.
Journal of Vascular Surgery Cases and Innovative Techniques|August 11, 2020
Mechanochemical and surgical ablation of an anomalous upper extremity marginal vein in CLOVES syndrome identifies <i>PIK3CA</i> as the culprit gene mutationYoung Lim, Arash Fereydooni, Anand Brahmandam, et al.
Pediatric Dermatology|November 9, 2021
Congenital verrucous plaquesMaria A Leszczynska, Kristan Schiele, Jose Cervantes, et al.
JAAD Case Reports|March 5, 2026
Characterizing superficial epidermolytic ichthyosis in a patient with KRT2 mutation responsive to ustekinumabMallory Zaino, Jordan Jones, Ronghua Hu, et al.
Journal of Clinical & Experimental Dermatology Research|October 21, 2022
Somatic Mosaicism in Blaschkolinear Inflammatory DisordersNicholas Theodosakis, Lauren Levy, Shawn Cowper, et al.
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion|July 14, 2016
Lethal Keratitis, Ichthyosis, and Deafness Syndrome Due to the A88V Connexin 26 MutationCarmen Esmer, Julio C Salas-Alanis, Oscar R Fajardo-Ramirez, et al.
International Journal of Dermatology|November 23, 2013
Mutations in TGM1 in Ecuadorians with autosomal recessive congenital ichthyosisHector Zambrano, Martha Montalvan, Jimmy Cabezas, et al.
JAMA Dermatology|July 21, 2016
Symptomatic Congenital Hemangioma and Congenital Hemangiomatosis Associated With a Somatic Activating Mutation in GNA11Tracy Funk, Young Lim, Ann M Kulungowski, et al.
The British Journal of Dermatology|February 28, 2023
Clinical features in adults with acquired cutis laxa: a retrospective reviewKatie A O'Connell, Morgan Schaefer, Lihi Atzmony, et al.
JAAD Case Reports|November 26, 2021
A novel <i>NFkB1</i> mutation linking pyoderma gangrenosum and common variable immunodeficiencyQisi Sun, Jeff R Gehlhausen, Marianna Freudzon, et al.
Pageof 4

Showing results (11-20 of 38) with videos related to

Sort By:
Pageof 4
JAMA Dermatology|August 1, 2019
Association of the Severity of Alopecia With the Severity of IchthyosisElana Putterman, Theodore Zaki, Leonard Milstone, et al.
Journal of Vascular Surgery Cases and Innovative Techniques|August 11, 2020
Mechanochemical and surgical ablation of an anomalous upper extremity marginal vein in CLOVES syndrome identifies <i>PIK3CA</i> as the culprit gene mutationYoung Lim, Arash Fereydooni, Anand Brahmandam, et al.
Pediatric Dermatology|November 9, 2021
Congenital verrucous plaquesMaria A Leszczynska, Kristan Schiele, Jose Cervantes, et al.
JAAD Case Reports|March 5, 2026
Characterizing superficial epidermolytic ichthyosis in a patient with KRT2 mutation responsive to ustekinumabMallory Zaino, Jordan Jones, Ronghua Hu, et al.
Journal of Clinical & Experimental Dermatology Research|October 21, 2022
Somatic Mosaicism in Blaschkolinear Inflammatory DisordersNicholas Theodosakis, Lauren Levy, Shawn Cowper, et al.
Revista De Investigacion Clinica; Organo Del Hospital De Enfermedades De La Nutricion|July 14, 2016
Lethal Keratitis, Ichthyosis, and Deafness Syndrome Due to the A88V Connexin 26 MutationCarmen Esmer, Julio C Salas-Alanis, Oscar R Fajardo-Ramirez, et al.
International Journal of Dermatology|November 23, 2013
Mutations in TGM1 in Ecuadorians with autosomal recessive congenital ichthyosisHector Zambrano, Martha Montalvan, Jimmy Cabezas, et al.
JAMA Dermatology|July 21, 2016
Symptomatic Congenital Hemangioma and Congenital Hemangiomatosis Associated With a Somatic Activating Mutation in GNA11Tracy Funk, Young Lim, Ann M Kulungowski, et al.
The British Journal of Dermatology|February 28, 2023
Clinical features in adults with acquired cutis laxa: a retrospective reviewKatie A O'Connell, Morgan Schaefer, Lihi Atzmony, et al.
JAAD Case Reports|November 26, 2021
A novel <i>NFkB1</i> mutation linking pyoderma gangrenosum and common variable immunodeficiencyQisi Sun, Jeff R Gehlhausen, Marianna Freudzon, et al.
Pageof 4