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Research 421–450 of 1000+
- The Body as the Universe: The Life Structure of the Danben Origin 身体即宇宙:丹体本源的生命结构
- High-magnification universal serial bus dermoscopy: A convenient alternative to direct microscopic examination
- Nail Involvement in Alopecia Areata: A Questionnaire-based Survey on Clinical Signs, Impact on Quality of Life and Review of the Literature
- Clinical Correlation Between Alopecia Areata and Salmon Patches: A Case Series
- Alopecia areata mit gutem Ansprechen auf Tofacitinib
- Topische Immuntherapie mit Diphenylcyclopropenon bei verschiedenen Typen der Alpecia areata: Assoziation zu klinischen Parametern und einem funktionellen Genpolymorphismus des Interleukin-6-Promotors
- 308-nm excimer laser therapy in alopecia areata
- Combination therapy with zinc gluconate and PUVA for alopecia areata totalis: an adjunctive but crucial role of zinc supplementation
- Pigmented contact dermatitis due to therapeutic sensitizer as complication of contact immunotherapy in alopecia areata
- Alopecia Areata
- Faculty Opinions recommendation of Treatment of alopecia areata with nonablative fractional laser combined with topical minoxidil.
- A case of dyschromatosis universalis
- Development of Indian Council of Medical Research (ICMR) Standard Treatment Workflows for Skin Diseases: A Step Toward Universal Health Coverage
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Differential diagnosis of trichotillomania by trichoscopy
- FOXN1 deficient nude severe combined immunodeficiency
- Hair loss in elderly women
- Nonscarring hair loss disorders
- Tofacitinib Treatment in Patients With Active COVID-19 Infection
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- Hair care, Therapies and Transplantation
- The Microbiome in Hair Disorders
- Hair Disorders
- A review on Hair Loss & Damage
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- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Excess granulation tissue and hair loss following acitretin
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions