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Research 151–180 of 321
- Netherton Syndrome With Trichorrhexis Invaginata “Bamboo Hair” Under Dermoscopy: Case Images
- [Monilethrix is a hereditary hair shaft disorder].
- A rare hair loss in children: Monilethrix
- Muir-torre syndrome in two families in Leicestershire, United Kingdom
- Overlap Between Ulerythema Ophryogenes and Keratosis Follicularis Spinulosa Decalvans: a Case Report
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- The Fate of Epidermal Tight Junctions in the stratum corneum: Their Involvement in the Regulation of Desquamation and Phenotypic Expression of Certain Skin Conditions
- Immunological and virological profile of children with chilblain‐like lesions and SARS‐CoV‐2
- Analogs of human genetic skin disease in domesticated animals
- 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
- Papular atrichia
- Ichthyosis with confetti: clinics, molecular genetics and management
- Pachyonychia Congenita-Associated Alopecia. A Microscopic Analysis Using Transverse Section Technique
- Papillon–Lefèvre Syndrome: A Rare Case Report of Two Brothers and Review of the Literature
- Ichthyosis linearis circumflexa in a child. Response to narrowband UVB therapy.
- Hypotrichosis with juvenile macular dystrophy
- Missense mutation Y449H of the K10 gene in a patient with severe epidermolytic ichthyosis
- 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
- Hair Shaft Disorders
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- Keratins and skin disease
- Prevalence of most common skin diseases in Europe: a population‐based study
- Efficient In Vivo Targeting of Epidermal Stem Cells by Early Gestational Intraamniotic Injection of Lentiviral Vector Driven by the Keratin 5 Promoter
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Avaliação dos efeitos adversos clínicos e alterações laboratoriais em pacientes com acne vulgar tratados com isotretinoína oral
- Keratins as an Inflammation Trigger Point in Epidermolysis Bullosa Simplex