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Research 61–90 of 1000+
- P78 Acrodermatitis enteropathica in children: clinical cases
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Björnstad Syndrome With Late‐Onset Alopecia Mimicking Androgenetic Alopecia: Histopathological and Genetic Findings
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Alopezien und Hypotrichosen im Kindesalter
- Frontal Fibrosing Alopecia: An Update on Pathogenesis, Diagnosis, and Treatment
- Madarosis
- Curly bare (cub), a new mouse mutation on chromosome 11 causing skin and hair abnormalities, and a modifier gene (mcub) on chromosome 5
- Pseudofolliculitis barbae; current treatment options
- Female pattern hair loss—An update
- Exploring the potential of herbal drugs for the treatment of hair loss
- Clinical Perspectives on Alopecia: From Hair Follicle Biology to Advanced Therapies
- SILENT PATCHES, LOUD SCIENCE: REVISITING ALOPECIA AREATA
- Premature greying of hair in children: A comprehensive review for pediatricians and primary care physicians
- Intrinsic and Extrinsic Factors Associated with Hair Graying (Canities) and Therapeutic Potential of Plant Extracts and Phytochemicals
- COMPREHENSIVE OVERVIEW ON THE PROBLEMS OF HAIR AND THE VARIOUS HERBAL APPROACHES TO TREAT THEM
- Potential etiological factors in frontal fibrosing alopecia
- 017 Lichen Planus Colocalized with Vitiligo: Coincidence?
- Androgenetska alopecija u žena
- Familial aggregation of phenotypic expression of premature hair hypopigmentation in the craniofacial region
- Pattern hair loss: Pathogenesis, clinical features, diagnosis, and management
- Origin, Clinical Presentation, and Diagnosis of Facial Hypermelanoses
- Scalp whorls
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- Pilomatricoma in Syndromic Contexts: A Literature Review and a Report of a Case in Apert Syndrome
- Breaking bald: Unraveling the mysteries of hair loss and modern treatments
- Congenital alopecia areata: a systematic review
- Moniletrix. Observación de esta infrecuente displasia pilosa en dos hermanos. Reporte clínico y dermatoscópico
- Telogen effluvium: Long term Covid-19 symptom
- How to diagnose a lipodystrophy syndrome