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Research 451–480 of 1000+
- Folliculin: A surprising molecular brake in the human hair follicle
- Pigmentary mosaicism: An update
- Keratin gene mutations in disorders of human skin and its appendages
- Ichthyosis
- Comedonal and Cystic Fibrofolliculomas in Birt-Hogg-Dube Syndrome
- Combined drug triads for synergic neuroprotection in retinal degeneration
- Analogs of human genetic skin disease in domesticated animals
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Tricorrexis nudosa localizada por aplicación compulsiva de minoxidil
- Ruxolitinib Rescues Multiorgan Clinical Autoimmunity in Patients with APS-1
- Discreet monilethrix: De novo mutation on the example of polish families
- Clouston’s syndrome: a rare case report
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Ptosis in childhood
- Genetic Basis of Male Pattern Baldness
- Dlx3 is a crucial regulator of hair follicle differentiation and cycling
- Trichoscopy in genetic hair shaft abnormalities
- A rare case of woolly hair with unusual associations
- Nilotinib-induced generalized keratosis pilaris: Report of a rare case
- The color of skin: white diseases of the skin, nails, and mucosa
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Abstracts
- Familial Frontal Fibrosing Alopecia
- Shock: A possible presenting manifestation of autoimmune polyendocrine syndrome type II
- Eruptive vellus hair cysts: An underdiagnosed entity
- Lipedema and lipedematous scalp: An overview
- Dercum Disease: Exploratory Therapeutic Approaches in the Absence of Standardized Medical Treatment—A Single Center Case Series
- Linear and Unilateral Basaloid Follicular Hamartoma Along Blaschko’s Lines in an Elderly Patient: A Rare Presentation
- LBODP010 A Case of Glucocorticoid Resistance Syndrome
- Generalized multiple eruptive milia in an infant – An unusual presentation