Results 161 to 170 of about 18,100 (230)

Type IV pityriasis rubra pilaris treated with ixekizumab. [PDF]

An Bras Dermatol
Ferreirinha A, João A, Brito Caldeira M.   +2 more
europepmc   +1 more source

Summary of Research: Apremilast in Japanese Patients with Palmoplantar Pustulosis: A Randomized, Phase 3 Trial. [PDF]

Dermatol Ther (Heidelb)
Terui T, Okubo Y, Kobayashi S, Morita A, Imafuku S, Tada Y, Abe M, Strober B, Gooderham M, Hara Y, Zhang W, Shimauchi J, Yaguchi M, Kimura T, Ogawa R, Amouzadeh H, Murakami M.   +16 more
europepmc   +1 more source

Drug reaction with eosinophilia and systemic symptoms syndrome secondary to bimekizumab. [PDF]

JAAD Case Rep
Fray K, Petrou IA, O'Callaghan D.
europepmc   +1 more source

Tofacitinib for the treatment of palmoplantar pustulosis: A multicenter prospective study. [PDF]

JAAD Int
Tao Y, Min S, Hua H, Xiao-Hong L, Tauseef H, Chirindo CV, Biao T, Yi-Huan J, Cheng Z, Chao C, Jian-Ping W.   +10 more
europepmc   +1 more source

Defining Histological Patterns in Inherited Ichthyoses: Toward a Diagnostic Algorithm Based on 66 Confirmed Cases. [PDF]

Dermatopathology (Basel)
Süßmuth K, Oji V, Bodes J, Jochum I, Muhs F, Komlosi K, Hausser I, Schmuth M, Traupe H, Fischer J, Metze D.   +10 more
europepmc   +1 more source

Case Report: Autosomal recessive palmoplantar keratoderma with additional bilateral hearing loss due to a pathogenic frameshift deletion in <i>FAM83G</i>. [PDF]

Front Med (Lausanne)
Mora-Gómez M, Feito M, Gallego-Zazo N, Maseda-Pedrero R, Sobral-Costas TG, Miranda-Alcaraz L, Vásquez-Amell V, Rodríguez-Canó M, Parra A, Cazalla M, Arias P, Silván C, Jiménez-Estrada JA, Ruiz-Pérez VL, Nevado J, Lapunzina P, Tenorio-Castano J.   +16 more
europepmc   +1 more source

Case Report: Secukinumab induced pustular eruption in a patient with ankylosing spondylitis. [PDF]

Front Med (Lausanne)
Tang Z, Liu X.
europepmc   +1 more source

A frameshift variation in the DSP gene causes a novel subtype of atypical epidermolytic palmoplantar keratoderma: Case report. [PDF]

Front Med (Lausanne)
Lin C, Chen H, Lai S, Huang S, Guo Z, Xie L, Zheng W, Lu J, Zeng Z, Wan C, Li L.   +10 more
europepmc   +1 more source

Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot. [PDF]

Hum Genome Var
Kumar S, Ahmed S, Incardona P, Cesarato N, Zhang Y, Natale MI, Khan MJ, Valinotto L, Ullah K, Ahmad W, Irurzun I, Krawitz PM, Liang B, Betz RC.   +13 more
europepmc   +1 more source