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Research 541–570 of 1000+
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- A single type of progenitor cell maintains normal epidermis
- Profile of 513 patients with alopecia areata: associations of disease subtypes with atopy, autoimmune disease and positive family history
- Viewpoint 1
- Hair today, gone tomorrow?: Teasing out details of hair growth
- Westwood Carolina Conference on Clinical Dermatology
- Ugreelig hår
- Acne and hidradenitis suppurativa
- Андроген-опосередковані й андрогенонезалежні причини алопеції та акне в жінок. Огляд літератури
- On the etiology of vitiligo and gray hair
- THE PATHOGENESIS OF ALOPECIA AREATA
- Female pattern hair loss: Clinico-laboratory findings and trichoscopy depending on disease severity
- Localized Autosomal Recessive Hypotrichosis Due to a Frameshift Mutation in the Desmoglein 4 Gene Exhibits Extensive Phenotypic Variability within a Pakistani Family
- An update of the pathogenesis of frontal fibrosing alopecia: What does the current evidence tell us?
- A novel monilethrix mutation in coil 2A of KRT86 causing autosomal dominant monilethrix with incomplete penetrance
- Alopecia in IL-10-deficient mouse pups is c-kit-dependent and can be triggered by iron deficiency
- Association of HSPA1B SNP rs6457452 with Alopecia Areata in the Korean Population
- Acquired progressive kinking of the hair in a prepubertal boy
- Substrate specific sulfatase activity from hair follicles in recessive X-linked ichthyosis
- A review of the etiologies, clinical characteristics, and treatment of canities
- <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy
- Sebaceous carcinoma arising at a chronic candidiasis skin lesion of a patient with keratitis-ichthyosis-deafness (KID) syndrome
- Male Pattern Androgenetic Alopecia
- A New Clinical Variant of Hereditary Localized Alopecia: Report of a Chinese Family Mapped to Chromosome 2p25.1–2p23.2
- Heterozygous deletion of the <i>NSDHL</i> gene in an Appenzeller Mountain Dog with verrucous epidermal keratinocytic nevi
- HLA‐B alleles associated with frontal fibrosing alopecia in Brazil may share similar peptide presentation and T‐cell interaction profiles
- Diagnosis and Management of Female Pattern Hair Loss
- Cheveu, vieillissement et environnement : aspects cliniques épidémiologiques
- THE GROWTH OF HUMAN HAIR IN NUDE MICE