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Research 961–990 of 1000+
- FGF5 is a crucial regulator of hair length in humans
- Causes and Management of Hypertrichosis
- Targeting the Complexity of In Vitro Skin Models: A Review of Cutting-Edge Developments
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- High Frequency of Symptomatic Zinc Deficiency in Infants in Northern Ethiopia
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Matriptase Expression and Zymogen Activation in Human Pilosebaceous Unit
- Rectangular-patterned occipital alopecia areata: A report of three cases
- Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention
- Renal tubular dysfunction presenting as recurrent hypokalemic periodic quadriparesis in systemic lupus erythematosus
- Hypoparathyroidism as the single major component for decades of autoimmune polyglandular syndrome type 1
- Nanostructured Drug Delivery Systems for Targeting 5-α-Reductase Inhibitors to the Hair Follicle
- Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets
- Difficult and rare forms of acne
- Nutritional Dermatoses in the Hospitalized Patient
- Diseases of Hair
- Congenital atrichia associated with nevus flammeus: A rare association
- Diseases of Hair
- Trichothiodystrophy
- Persistent hyperparathyroidism in vitamin D-dependent rickets type 2A does not prevent normalization of hypophosphatemia or healing of the rickets
- Cutaneous Manifestations in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy (APECED): A Comprehensive Review
- Receptors in trichology: Hot spots for hair regeneration
- Hereditary 1,25‐Dihydroxyvitamin D‐Resistant Rickets in a Pomeranian Dog Caused by a Novel Mutation in the Vitamin D Receptor Gene
- Ultra‐structural hair alterations in Friedreich's ataxia: A scanning electron microscopic investigation
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation