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Research 211–240 of 1000+
- Folliculosebaceous cystic hamartoma with hair shaft fragments.
- Identification of factors contributing to phenotypic divergence via quantitative image analyses of autosomal recessive woolly hair/hypotrichosis with homozygous c.736T>A<i>LIPH</i>mutation
- Linear immunoglobulin A/immunoglobulin G bullous dermatosis associated with Vogt-Koyanagi-Harada disease
- Azathioprine-induced Agranulocytosis and Severe Alopecia After Kidney Transplantation Associated With a NUDT15 Polymorphism: A Case Report
- Case Report. Kerion Celsi effectively treated with terbinafine. Characteristics of kerion Celsi in the elderly in Japan
- A Case of Relapsed Leprosy Successfully Treated With Sparfloxacin
- ROLLED HAIRS AND HYPERTRICHOSIS
- The Secrets of Beautiful Hair: Why is it Flexible and Elastic?
- Ultrastructural characteristics of trichilemmal cysts: report of two cases
- Moth-Eaten Symptomatic Syphilitic Alopecia Associated with Human Immunodeficiency Virus—A Case Report
- Cicatricial alopecia of the scalp as a manifestation of IgG4-related disease mimicking acne keloidalis nuchae
- Nemolizumab Treatment for Severe Atopic Dermatitis Led to the Simultaneous Improvement of Coexisting Refractory Alopecia Areata: A Case Report
- Vogt-Koyanagi-Harada Disease in which Poliosis and Alopecia Occurred after a Long Period of Time.
- Postzygotic KRAS G12C mutation, associated with various malignancies, is also underling epidermal nevus syndrome
- Letter from Brisbane [Letters to editor]
- Mutations in the Desmoglein 4 Gene Are Associated with Monilethrix-like Congenital Hypotrichosis
- Identification and characterization of Birt–Hogg–Dubé associated renal carcinoma
- Congenital hair loss disorders: Rare, but not too rare
- Changes in the sebaceous gland in patients with male pattern hair loss (androgenic alopecia)
- The effect of night shift work on the expression of clock genes in beard hair follicle cells
- Subcutaneous Chest Abscess Caused by Candida albicans Infection Following Laparoscopic Cholecystectomy in an Immunocompetent Patient: A Case Report
- Single nucleotide polymorphisms associated with elevated alanine aminotransferase in patients receiving asunaprevir plus daclatasvir combination therapy for chronic hepatitis C
- Multiple desmoplastic trichoepitheliomas with ossification and cholesterol deposition
- Cronkhite–Canada Syndrome With Multiple Mesenteric Lymphadenopathy: A Case Report
- Antitermitic Activity of Cunninghamia lanceolata Heartwood Components against Reticulitermes speratus
- A homozygous single T deletion found in the GGCX gene with PXE-like phenotypes
- A replication study confirmed the EDAR gene to be a major contributor to population differentiation regarding head hair thickness in Asia
- Polymorphisms in the Human High Sulfur Hair Keratin-associated Protein 1, KAP1, Gene Family
- A Homozygous Nonsense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia
- Tufted hair folliculitis developing in a recalcitrant lesion of pemphigus vulgaris