Results 121 to 130 of about 13,745 (220)

Infantile sporadic epidermolytic hyperkeratosis: a case report [PDF]

open access: gold, 2018
Ghita Senhaji   +5 more
openalex   +1 more source

Novel and recurrent mutations in keratin 1 cause epidermolytic ichthyosis and palmoplantar keratoderma [PDF]

open access: yes, 2019
Jury, C. S.   +5 more
core   +2 more sources

Autosomal dominant non-epidermolytic palmoplantar hyperkeratosis in a Nigerian girl

open access: yesNigerian Journal of Paediatrics
Palmoplantar keratoderma (PPK) is a hereditary cutaneous disorder characterized by a marked hyperkeratosis of the palms and soles. A variant that was inherited in an autosomal dominant form was highlighted in a 20-month-old girl-child.
Anigilaje EA, Dzuachii DO
doaj  

A Novel Glutamic Acid to Aspartic Acid Mutation Near the End of the 2B Rod Domain in the Keratin 1 Chain in Epidermolytic Hyperkeratosis

open access: bronze, 1999
Jum-Mo Yang   +7 more
openalex   +1 more source

Extremely severe palmoplantar hyperkeratosis in a generalized epidermolytic hyperkeratosis patient with a keratin 1 gene mutation [PDF]

open access: bronze, 2011
R. Osawa   +8 more
openalex   +1 more source

Isolated Epidermolytic Acanthoma in a Renal Transplant Recipient [PDF]

open access: yes, 2011
Ackerman   +12 more
core   +2 more sources

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