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Research 781–810 of 1000+
- Phototherapy of androgenetic alopecia with low level narrow band 655-nm red light and 780-nm infrared light
- Approach to the patient with hair loss
- A Case to Tear One's Hair Out: Trichotillomania in Wilson's Disease
- Disseminated tinea incognito due to Trichophyton violaceum in a healthy child
- Overlap Between Ulerythema Ophryogenes and Keratosis Follicularis Spinulosa Decalvans: a Case Report
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- BIPHENOTYPIC LEUKAEMIA
- Clinical Outcomes of Ritlecitinib in Treatment-Refractory Alopecia Areata: A Single-Center Real-World Study
- Alopecia areta: a review
- Ophthalmologic Comorbidities in Alopecia Areata
- A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene
- Reversing alopecia universalis with classical homeopathy: A case study
- An Interesting Case of X-linked Hypohidrotic Ectodermal Dysplasia
- LIFEHOUSE’s Functional Nutrition Examination (Physical Exam, Anthropometrics, and Selected Biomarkers) Informs Personalized Wellness Interventions
- A RARE CASE OF VITAMIN D DEPENDENT RICKETS TYPE-2A PRESENTED AS ALOPECIA TOTALIS
- Hair Loss and Hirsutism Management
- Contents
- Role of estrogen receptor signaling in the control of the hair follicle cycle
- Depression from a physical symptom.
- Nailfold capillaroscopy alterations in androgenetic alopecia: A cross-sectional study
- Androgenetic Alopecia
- Hair Growth Defects in Insig-Deficient Mice Caused by Cholesterol Precursor Accumulation and Reversed by Simvastatin
- Drug-induced male infertility: a real-world study using FAERS and EudraVigilance databases
- Inherited Disorders of the Hair
- Comma hairs: A dermatoscopic marker for tinea capitis
- Alopecia areata: Clinical presentation, diagnosis, and unusual cases
- Comorbidities in alopecia areata: A systematic review and meta-analysis
- Corneodesmosin gene ablation induces lethal skin-barrier disruption and hair-follicle degeneration related to desmosome dysfunction
- Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease
- 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.