Tissue-specific expression and functional role of keratin 1 in sheep horn development. [PDF]
Mei Q +7 more
europepmc +1 more source
Disorders of keratinisation: from rare to common genetic diseases of skin and other epithelial tissues [PDF]
Irvine, Alan D, McLean, WH Irwin
core +1 more source
Ophthalmic phenotype associated with a novel mutation in <i>LAMB3</i> gene linked to uncommon Intermediate Junctional Epidermolysis Bullosa. [PDF]
Alzaben KA +5 more
europepmc +1 more source
The role of the skin microbiome in inherited ichthyoses: A systematic review. [PDF]
Metyovinyi Z +4 more
europepmc +1 more source
Ocular Manifestations Leading to the Diagnosis of Ichthyosis: A Case Report. [PDF]
Khadamy J.
europepmc +1 more source
Ichthyosis bullosa of Siemens : a distinct type of epidermolytic hyperkeratosis
Ursula Lenzner +6 more
openalex +1 more source
Epidermolytic Hyperkeratosis Type 1 with a New Heterozygous Mutation in KRT1 Gene: A Case Report
Maitha Abdulla Aljuwaied +7 more
openalex +1 more source
Arrhythmogenic cardiomyopathy in children, on the link between injurious mutations and inflammation: Two case reports and review of the literature. [PDF]
Nikitina E +7 more
europepmc +1 more source
Infant with a hereditary blistering disorder: an interesting case in the NICU. [PDF]
Tchignaha R +4 more
europepmc +1 more source
Severe palmoplantar keratoderma: a cutaneous complication from sub-optimally controlled type 2 diabetes. [PDF]
Iqbal F, Phan K, Cheung WN.
europepmc +1 more source

