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- Zebrafish Model of Hereditary Pigmentary Disorders
- Hair science and technology
- Analogs of human genetic skin disease in domesticated animals
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- Erythromelanosis Follicularis Faciei et Colli: A Case Report
- Inherited Disorders of the Hair
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Drug-Induced Skin, Nail and Hair Disorders
- SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Gender aspects in skin diseases
- Dermatoses of pregnancy
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- Clinical Role of Oral Vitamin C and E Therapy in Skin and Hair Disorders
- Cutaneous manifestations of metabolic diseases: uncommon presentations
- National scientific medical meeting 1996 abstracts
- Hereditary, Congenital, and Acquired Alopecias
- The PER3 rs772027021 SNP induces pigmentation phenotypes of dyschromatosis universalis hereditaria
- Hair and scalp disorders
- Hereditary, Congenital, and Acquired Alopecias
- Hair follicles, their disorders and their opportunities
- A CLINICAL STUDY OF CUTANEOUS MANIFESTATIONS IN PATIENTS WITH THYROID DISORDERS
- Healing hair naturally: A focus on herbal treatment for hair disorders
- Clinical Case Notes. Lipoid proteinosis: a rare disorder with pathognomonic lid lesions
- Pregnancy and Skin
- General Dermatology
- Marie Antoinette Syndrome
- Acquired scalp alopecia. Part I: A review
- Madarosis, milphosis, eyelash trichomegaly, and dermatochalasis