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Research 781–810 of 1000+
- Myotonic Dystrophy—A Progeroid Disease?
- Novel de novo pathogenic variant in the <i>ODC1</i> gene in a girl with developmental delay, alopecia, and dysmorphic features
- Birt–Hogg–Dubé syndrome: from gene discovery to molecularly targeted therapies
- A kindred with mutant IKAROS and autoimmunity
- Update on hidradenitis suppurativa: connecting the tracts
- Comedonal and Cystic Fibrofolliculomas in Birt-Hogg-Dube Syndrome
- Disruption of tubular Flcn expression as a mouse model for renal tumor induction
- Unraveling the complex role of MAPT-containing H1 and H2 haplotypes in neurodegenerative diseases
- Three Streams for the Mechanism of Hair Graying
- Identification of somatic and germline mosaicism for a keratin 5 mutation in epidermolysis bullosa simplex in a family of which the proband was previously regarded as a sporadic case
- Analysis of hidradenitis suppurativa–linked mutations in four genes and the effects of PSEN1-P242LfsX11 on cytokine and chemokine expression in macrophages
- Management of Androgenetic Alopecia
- Treatment of Keratosis Pilaris With 810-nm Diode Laser
- Nilotinib-Induced Keratosis Pilaris
- Treatment options for androgenetic alopecia: Efficacy, side effects, compliance, financial considerations, and ethics
- Beyond the Hot Comb: Updates in Epidemiology, Pathogenesis, and Treatment of Central Centrifugal Cicatricial Alopecia from 2011 to 2021
- Association of epidemiological and biochemical factors with premature graying of hair: A case–control study
- Use of dermoscopy in the diagnosis of temporal triangular alopecia
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- An epistatic effect of KRT25 on SP6 is involved in curly coat in horses
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Pili annulati with fragility: Electron microscopic findings of a case
- A rare case of woolly hair with unusual associations
- Molecular Basis of Androgenetic Alopecia
- Update on Melasma—Part I: Pathogenesis
- Eruptive vellus hair cyst: An uncommon and underdiagnosed entity
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Smoothened receptor inhibitor vismodegib for the treatment of basal cell carcinoma: a retrospective analysis of efficacy and side effects
- Polycystic ovary syndrome