Results 161 to 170 of about 1,914 (209)

Tissue-specific expression and functional role of keratin 1 in sheep horn development. [PDF]

open access: yesFront Vet Sci
Mei Q   +7 more
europepmc   +1 more source

Ophthalmic phenotype associated with a novel mutation in <i>LAMB3</i> gene linked to uncommon Intermediate Junctional Epidermolysis Bullosa. [PDF]

open access: yesAm J Ophthalmol Case Rep
Alzaben KA   +5 more
europepmc   +1 more source

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

open access: yesJAAD Int
Metyovinyi Z   +4 more
europepmc   +1 more source

Ichthyosis bullosa of Siemens : a distinct type of epidermolytic hyperkeratosis

open access: green, 1996
Ursula Lenzner   +6 more
openalex   +1 more source

Epidermolytic Hyperkeratosis Type 1 with a New Heterozygous Mutation in KRT1 Gene: A Case Report

open access: hybrid
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]

open access: yesWorld J Clin Pediatr
Nikitina E   +7 more
europepmc   +1 more source

Infant with a hereditary blistering disorder: an interesting case in the NICU. [PDF]

open access: yesOxf Med Case Reports
Tchignaha R   +4 more
europepmc   +1 more source

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