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Research 61–90 of 69
- Genetic Variants and Protective Immunity against SARS-CoV-2
- Autophagy Dysfunction: The Kernel of Hair Loss?
- Pattern of Nail and Hair Disorders in the Elderly at a Tertiary Health Centre
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- HR Gene Variants Identified in Mexican Patients with Alopecia Areata
- Selection signatures for fiber production in commercial species: A review
- Tru9I Variant as a Novel Genetic Marker for Vitamin D Deficiency in Alopecia Areata
- Genetic diversity and phylogeography of the endemic species Prunus mira in the Qinghai–Tibetan Plateau
- C‐reactive protein as a novel biomarker for vitamin D deficiency in alopecia areata
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- Management of congenital ichthyoses: European guidelines of care, part two
- Care of the newborn with ichthyosis
- Harlequin fetus with abnormal lamellar granules and giant mitochondria
- New developments in the molecular treatment of ichthyosis: review of the literature
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- First Symposium of Ichthyosis Experts
- A null mutation in the cystatin M/E gene of ichq mice causes juvenile lethality and defects in epidermal cornification
- Hair follicles modulate skin barrier function
- Dynamics of Hair Follicle Morphogenesis and Skin Homeostasis
- Disorders of Keratinization
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Ichthyosis with confetti: a rare diagnosis and treatment plan
- ИХТИОЗ АРЛЕКИНО: КЛИНИЧЕСКИЙ СЛУЧАЙ
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders