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Research 661–690 of 1000+
- A rare case of woolly hair with unusual associations
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Atrichia with papular lesions
- Case report of connubial frontal fibrosing alopecia
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Alopecia Areata of the Nails: Diagnosis and Management
- Epidemiology of alopecia areata in Hispanic/Latinx patients
- Association of frontal fibrosing alopecia and contact allergens in everyday skincare products in Hispanic females: a case-control study
- Prevalence of Skin Manifestations in Thyroid Disorders
- A systematic review and meta‐synthesis of qualitative studies of alopecia: Managing identity and appearance changes
- Folliculotropic Mycosis Fungoides: Update on Diagnosis, Clinicopathological Stage, and Management
- Alopecia Areata in Sub-Saharan Africa: A Scoping Review Protocol on Epidemiology, Clinical Presentation, Burden, Treatment, and Evidence Gaps.
- Adipose Tissue‐Derived Exosomes in the Treatment of Lichen Planopilaris: A Case Report
- Mesenchymal Stem Cell Therapy in Alopecia Areata: Visual and Molecular Evidence from a Mouse Model
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Multifocal alopecia of the scalp, axillae, and body
- A review of isotretinoin in the treatment of frontal fibrosing alopecia
- Upadacitinib for Alopecia Areata in Different Backgrounds: A Case Series
- Autoinmune Alopecia/Alopecia Areata
- Co-occurrence of Progressive Hemifacial atrophy due to Morphea with homolateral segmental Vitiligo: a case report
- Unusual Cause of Chronic Diarrhea: Cronkhite-Canada Syndrome
- Frontal fibrosing alopecia: follow-up of a brazilian group
- Acquired Progressive Kinking of the Hair
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Successful treatment of alopecia universalis with abrocitinib: a case report
- Demographic Characteristics and Association of Serum Vitamin B12, Ferritin and Thyroid Function with Premature Canities in Indian Patients from an Urban Skin Clinic of North India: A Retrospective Analysis of 71 Cases.
- Alopecia universalis during treatment with leflunomide and adalimumab - Case report
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Beyond the Surface: Understanding Demodex and Its Link to Blepharitis and Facial Dermatoses
- Efficacy of diphenylcyclopropenone in alopecia areata: a comparison of two treatment regimens