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Research 30 of 620
- Macular Abnormalities Associated With 5α-Reductase Inhibitor
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Dutasteride/finasteride
- Mimicking Hair Disorders by Genetic Manipulation of Organ-Cultured Human Hair Follicles
- Hypotrichosis with juvenile macular dystrophy
- Optical Coherence Tomography Angiography Findings in Polycystic Ovary Syndrome
- Mutant laboratory mice with abnormalities in hair follicle morphogenesis, cycling, and/or structure: An update
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Lithium therapy associated with hidradenitis suppurativa: Case report and a review of the dermatologic side effects of lithium
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Management of Toxicities of Targeted Therapies
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Nail abnormalities in patients with vitiligo
- Hair Loss in Children
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Age-Related Macular Degeneration in Patients with Androgenetic Alopecia: Could the Monocyte/HDL Ratio Be the Link?
- Dermatopathology and molecular genetics
- Management of Dermatologic Toxicities
- Marie-unna hereditary hypotrichosis
- Hair and Nail Manifestations of Systemic Disease
- The ophthalmological complications of targeted agents in cancer therapy: what do we need to know as ophthalmologists?
- Cutaneous features of myotonic dystrophy types 1 and 2: Implication of premature aging and vitamin D homeostasis
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Hair Bundle Defects and Loss of Function in the Vestibular End Organs of Mice Lacking the Receptor-Like Inositol Lipid Phosphatase PTPRQ
- TONGUE, RED
- Ichthyosis hystrix