Results 131 to 140 of about 14,748 (240)

Skin Fragility-Woolly Hair Syndrome (SFWHS): A Case Report. [PDF]

open access: yesCureus
Almousa A   +4 more
europepmc   +1 more source

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

open access: yesFront Med (Lausanne)
Lin C   +10 more
europepmc   +1 more source

A novel microdeletion in LOR causing autosomal dominant loricrin keratoderma [PDF]

open access: yes, 2014
Barnicoat, A   +8 more
core   +1 more source

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

open access: yesAn Bras Dermatol
Ferreirinha A   +2 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]

open access: yesFront Med (Lausanne)
Mora-Gómez M   +16 more
europepmc   +1 more source

Loss-of-function variants in SERPINA12 underlie autosomal recessive palmoplantar keratoderma.

open access: yesJournal of Investigative Dermatology, 2020
J. Mohamad   +14 more
semanticscholar   +1 more source

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