Results 71 to 80 of about 238,615 (114)

Sporadic Case of Ichthyosis Bullosa of Siemens in an Infant: A Rare Case. [PDF]

Indian J Dermatol, 2021
Vijay A, Kumar A, Saini S, Agarwal S.
europepmc   +1 more source

Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions. [PDF]

Int J Mol Sci, 2023
Pondeljak N, Lugović-Mihić L, Tomić L, Parać E, Pedić L, Lazić-Mosler E.   +5 more
europepmc   +1 more source

Ichthyoses-A Clinical and Pathological Spectrum from Heterogeneous Cornification Disorders to Inflammation. [PDF]

Dermatopathology (Basel), 2021
Metze D, Traupe H, Süßmuth K.
europepmc   +1 more source

Congenital Segmental Erosions and Hyperkeratotic Plaques in a Male Infant: A Quiz. [PDF]

Acta Derm Venereol
Yilmaz K, Evers C, Brandau O, Schaarschmidt ML, Géraud C.   +4 more
europepmc   +1 more source

Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing <i>Trichophyton rubrum</i> Infection and Blocker Displacement Amplification for Mosaic Mutation Detection. [PDF]

Biomedicines
Liu J, Fu Y, Zhang Q, Chen Q, Yang Y, Xue Y, Ren Y.   +6 more
europepmc   +1 more source

Novel peeling skin condition in neonatal Pacific walruses, Saint Lawrence Island, Alaska, USA. [PDF]

J Vet Diagn Invest, 2023
Stimmelmayr R, Rotstein D, Sanchez S, Baird A, Sheffield G, Snyder JA.   +5 more
europepmc   +1 more source

Hypergranulotic Dyscornification - Alba Variant. [PDF]

Indian J Dermatol
SriRam CK, Krishnaram AS, Shibani I, Priya SK.   +3 more
europepmc   +1 more source

From clinic to microscope: A study of clinicopathological concordance in 5000 skin biopsies from a tertiary care center. [PDF]

J Postgrad Med
Singh S, Thirumalaiswamy A, Kharkar V, Mahajan S, Joshi R, Sharath SM.   +5 more
europepmc   +1 more source

The role of the skin microbiome in inherited ichthyoses: A systematic review. [PDF]

JAAD Int
Metyovinyi Z, Szondy I, Kiss N, Ostorházi E, Medvecz M.   +4 more
europepmc   +1 more source

Applications of CRISPR-Cas9 in Gene Therapy: Generating a cell culture model and developing tools for a sheep model of Epidermolytic Ichthyosis

Epidermolytic ichthyosis is a hereditary skin condition caused by mutations in the KRT1 or KRT10 genes that alter the structure of the associated keratin proteins leading to cytoskeleton fragility, cellular collapse and loss of tissue integrity.
Blaine, Jade
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