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- Existence of Neural Crest–Derived Progenitor Cells in Normal and Fuchs Endothelial Dystrophy Corneal Endothelium
- Keratin expression by corneal and limbal stem cells during development
- Dermatopathia Pigmentosa Reticularis with Salzmann’s nodular degeneration of cornea: A rare association
- Keratosis follicularis spinulosa decalvans: a family study of seven male cases and six female carriers.
- Keratin disorders: from gene to therapy
- News in brief
- Roles of Wnt7a in embryo development, tissue homeostasis, and human diseases
- Mechanotransductive Differentiation of Hair Follicle Stem Cells Derived from Aged Eyelid Skin into Corneal Endothelial-Like Cells
- Co-factors of LIM domains (Clims/Ldb/Nli) regulate corneal homeostasis and maintenance of hair follicle stem cells
- Séquelles cutanéomuqueuses et oculaires des SJS et de Lyell
- Alterations in Corneal Sensitivity, Staining and Biomechanics of Alopecia Areata Patients: Novel Findings in a Case-Control Study
- Antiviral drugs prolong survival in murine recessive dystrophic epidermolysis bullosa
- Episodic Bilateral Corneal Edema Caused by Hair Groom Gel
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Inherited Epidermolysis Bullosa: A Clinical Case
- Disrupted Ectodermal Organ Morphogenesis in Mice with a Conditional Histone Deacetylase 1, 2 Deletion in the Epidermis
- Alginate-Based Composites for Corneal Regeneration: The Optimization of a Biomaterial to Overcome Its Limits
- Relation of Selenium, Vitamin E and Other Factors to Muscular Dystrophy in the Rabbit
- Characterization of Bsk mice: I. The Bsk mutation does not involve a recombination of cornea-specific keratin 12 and skin-specific hair keratin genes.
- Exploring lncRNA-Mediated Mechanisms in Muscle Regulation and Their Implications for Duchenne Muscular Dystrophy
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Inherited epidermolysis bullosa: clinical and therapeutic aspects
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Regenerative Medicine of Epidermal Structures
- Clinical Case Notes. Lipoid proteinosis: a rare disorder with pathognomonic lid lesions
- Clinical Case Notes. Castleman's disease of the lacrimal gland
- Diseases of Periocular Hair
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome