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Research 271–300 of 1000+
- Dermoscopy: A rapid bedside tool to assess monilethrix
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- A Case of Loose Anagen Hair Syndrome in a Southeast Asian Boy
- Coexisting trichorrhexis nodosa and pili annulati: a case report of hair shaft abnormalities in a syrian family
- The Wound Reporting in Animal and Human Preclinical Studies (WRAHPS) Guidelines
- Successful topical minoxidil treatment for hair density and length in trichorhinophalangeal syndrome type 1
- Focused Review on Metal Nanoparticles in Hair Regeneration and Alopecia: Insights into Mechanisms, Assessment Techniques, Toxicity, Regulatory and Intellectual Property Perspectives
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- Trichoscopy in genetic hair shaft abnormalities
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Zinc and Zinc Transporters in Dermatology
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Follicular and Scarring Disorders in Skin of Color: Presentation and Management
- Oral minoxidil in trichology: A review
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma
- Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Growth Hormone and the Human Hair Follicle
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Epidermal patterning and induction of different hair types during mouse embryonic development
- Wnt Signaling Across Adult Skin Mini-Organs: Interfollicular Epidermis, Hair Follicle, and Nail—Implications for Disease and Regeneration
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- <i>WNT10A</i> , dermatology and dentistry
- Proceedings of the Ninth World Congress for Hair Research (2015)
- Racial and Gender Influences on Skin Disease
- A Child with Nonscarring Alopecia