Results 121 to 130 of about 13,745 (220)
Infantile sporadic epidermolytic hyperkeratosis: a case report [PDF]
Ghita Senhaji+5 more
openalex +1 more source
Novel and recurrent mutations in keratin 1 cause epidermolytic ichthyosis and palmoplantar keratoderma [PDF]
Jury, C. S.+5 more
core +2 more sources
Autosomal dominant non-epidermolytic palmoplantar hyperkeratosis in a Nigerian girl
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
Extremely severe palmoplantar hyperkeratosis in a generalized epidermolytic hyperkeratosis patient with a keratin 1 gene mutation [PDF]
R. Osawa+8 more
openalex +1 more source
Isolated Epidermolytic Acanthoma in a Renal Transplant Recipient [PDF]
Ackerman+12 more
core +2 more sources
Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions. [PDF]
Pondeljak N+5 more
europepmc +1 more source
Antibiotic Therapy in a Boy Affected by Generalized Epidermolytic Hyperkeratosis [PDF]
Stefano Cambiaghi, E. Ermacora
openalex +1 more source