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Research 211–240 of 368
- Early-onset recipient-site necrosis after FUE hair transplantation complicated by <i>Pseudomonas aeruginosa</i> infection: a case report
- An Autosomal Recessive Woolly Hair/Hypotrichosis Case with LIPH Mutation in a Turkish Patient
- Netherton Syndrome – Responding to Oral Retinoids
- Dermatology resident comfort level treating hair conditions related to patients with skin of color
- Hair Evaluation in Orthodontic Patients with Oligodontia
- Doctor, my armpit hair has turned yellow! Malodorous yellowish axillary hair in an adolescent patient
- Thermal Modifications of Ethnic Hair
- 675 Hair loss in hephaestin knockout mice is associated with iron deficiency
- Changes in cuticle of scalp hair in mild acquired zinc deficiency: A study using scanning electron microscopy
- Scalp Dermatology for the Hair Restoration Surgeon
- Hair casts (pseudonits)
- Case Report: 7 Year-Old Saudi Female with Monilethrix
- Trichoscopy in genetic hair shaft abnormalities
- Frontal Fibrosing Alopecia
- Pathogenesis in pili torti: morphological study
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Dermoscopy in General Dermatology: A Practical Overview
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Trichoscopy in alopecias: Diagnosis simplified
- Alopecia Areata: An Updated Review for 2023
- Metabolites from Macroalgae and Its Applications in the Cosmetic Industry: A Circular Economy Approach
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Pharmacologic interventions in aging hair
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Female pattern alopecia: current perspectives
- Relevance of trichoscopy in the differential diagnosis of alopecia: A cross-sectional study from North India
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- SKIN AND HAIR COSMETIC ISSUES IN WOMEN OF COLOR
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome