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Research 661–690 of 1000+
- Immune cell regulation of the hair cycle
- Hormone und Haarwachstum
- Hair Loss in Systemic Disease
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- The clinical spectrum of parathyroid disease
- EXPLORATION OF MEDICINAL PLANTS USED BY THE MALAYALI TRIBES OF KOLLI HILLS, TAMILNADU, INDIA
- An effective new therapy for burn wounds
- Ingestion of topical steroid triggering pustular psoriasis?
- Hidradenitis suppurativa: a new therapeutic approach for an old disease
- Lichen Planopilaris
- Role of Androgen in Mesenchymal Epithelial Interactions in Human Hair Follicle
- Hidradenitis Suppurativa and Wound Management
- Frontal Fibrosing Alopecia
- Beyond Coincidence in Neurofibromatosis Type 1: Becker Nevus Adjacent to Plexiform Neurofibroma with Brachial Plexus Involvement and Integrated Mechanistic Illustration
- Widespread and eruptive comedonal lesions with alopecia
- Graham Little-Lassueur Syndrome with Hypertrophic Lichen Planus in a Patient with Chronic Hepatitis C
- Human hair shaft proteomic profiling: individual differences, site specificity and cuticle analysis
- Features Associated With Quality of Life Impairment in Hidradenitis Suppurativa Patients
- Animal and in vitro Models for the Study of Hair Follicles
- Functional characterization of soybean strigolactone biosynthesis and signaling genes in Arabidopsis MAX mutants and GmMAX3 in soybean nodulation
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Lesson of the week: Haemochromatosis as an endocrine cause of subfertility
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers
- Use of topical clascoterone for the treatment of hidradenitis suppurativa
- Nodules on the hair: A rare case of mixed piedra
- Graham‐Little Piccardi Lassueur syndrome and review of the literature
- Monilethrix, a rare inherited hair shaft disorder in siblings
- Stage-Specific Embryonic Antigen-4 (SSEA-4) as a Distinguishing Marker between Eccrine and Apocrine Origin of Ducts of Sweat Glands
- Diffuse hair loss in Addison disease: A reason for X-linked adrenoleukodystrophy screening