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Research 91–120 of 1000+
- Trichoscopic evaluation of frontal hairline recession in Egyptian female patients
- Marie‐Unna Hereditary Hypotrichosis or Autosomal Recessive Hereditary Hypotrichosis with Woolly Hair: The Diagnostic Dilemma of Labeling Cases with Hypotrichosis
- Unique Hair Properties that Emerge from Combinations of Multiple Races
- Transplantation of autologous single hair units heals chronic wounds in autosomal recessive dystrophic epidermolysis bullosa: A proof-of-concept study
- A retrospective study on the characteristics of androgenetic alopecia among Asian races in the National Skin Centre, a tertiary dermatological referral centre in Singapore.
- Faculty Opinions recommendation of Association of topical minoxidil with autosomal recessive woolly hair/hypotrichosis caused by LIPH pathogenic variants.
- Identification of compound heterozygous mutations in <i>AP1B1</i> leading to the newly described recessive keratitis–ichthyosis–deafness (KIDAR) syndrome
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- 441 Anti-melanoma gene signature in dermal sheath fibroblasts from scalp hair follicles in Recessive Dystrophic Epidermolysis Bullosa (RDEB)
- Successful Treatment of Hair Loss and Restoration of Natural Hair Color in Patient with Alopecia Areata Due to Psychological Disorder Using Exosomes: Case Report with 6-Month Follow-Up
- Rose stem cell‐derived exosomes for hair regeneration enhancement via noninvasive electroporation in androgenetic alopecia
- Mechanical forces in skin disorders
- The character “hairless” in the mouse
- Quality of life and psychosocial impact of scarring and non‐scarring alopecia in women
- Balding: A New Mutation on Mouse Chromosome 18 Causing Hair Loss and Immunological Defects
- First symposium on natural gene therapy of the skin
- The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome
- Lichen planus pigmentosus and lichen planopilaris
- Mesenchymal Stem Cells for the Treatment of Skin Diseases
- Natural variation in trichome density and biochemistry in Antirrhinum
- 688 Precise and efficient editing of the COL7A1 gene in RDEB derived iPSCs with CRISPR/Cas9 and prime editing
- Investigating the relationship between self-esteem and body image concern and self-compassion in women with female pattern hair loss
- TERMIS ‐ AMERICAS Toronto, Ontario, Canada July 10–13, 2022
- Moniletrix. Observación de esta infrecuente displasia pilosa en dos hermanos. Reporte clínico y dermatoscópico
- 314 Molecular genetic dissection of ILVEN leads to successful targeted therapy
- Disorders of Keratinization
- Research Snippets
- Assessment of quality of life and self‐esteem in male patients with androgenetic alopecia before and after hair transplantation
- Prevalence of Male and Female Pattern Hair Loss in Maryborough
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia