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Research 151–180 of 313
- Folliculin: A surprising molecular brake in the human hair follicle
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Comparative trail on efficacy of topical contact immunotherapy with dinitrochlorobenzene and diphenylcyclopropenone in alopecia areata
- Tricholemmoma and tricholemmal carcinoma and Cowden syndrome
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Immunological and virological profile of children with chilblain‐like lesions and SARS‐CoV‐2
- Alopecia Areata Is Associated with an Increased Risk for Prediabetes and Obesity: A Nationwide Case—Control Study
- 155 Exploring perceived quality of life in middle- to old-aged patients with inherited ichthyosis: a qualitative study
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- Hair Shaft Disorders
- Papular atrichia
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- Comedonal and Cystic Fibrofolliculomas in Birt-Hogg-Dube Syndrome
- Structural mechanism of TRPV3 channel inhibition by the plant‐derived coumarin osthole
- Activation of TRPV3 Inhibits Lipogenesis and Stimulates Production of Inflammatory Mediators in Human Sebocytes—A Putative Contributor to Dry Skin Dermatoses
- The Genetics of Human Skin Disease
- 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
- No Evidence That Human Papillomavirus Is Responsible for the Aggressive Nature of Recessive Dystrophic Epidermolysis Bullosa–Associated Squamous Cell Carcinoma
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Off-label uses of retinoids in dermatology
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Value of dermoscopy for the diagnosis of monilethrix
- Early diagnosis of ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis syndrome: A case report
- First Symposium of Ichthyosis Experts
- Netherton Syndrome – Responding to Oral Retinoids
- Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma