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Research 571–600 of 1000+
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- Hirsutism in Women.
- Retinol dehydrogenase 12 (RDH12): Role in vision, retinal disease and future perspectives
- An Assessment of Quality-of-Life Following Tissue Expansion in Pediatric Patients
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Polarized microscopy in genetic hair disorders: case series
- Case 1: Clitoromegaly, Oligomenorrhea, and Hirsutism in a 17-year-old Transgender Male
- Bachmann–Bupp syndrome and treatment
- Alopecia in Patients with Collagen VI-Related Myopathies: A Novel/Unrecognized Scalp Phenotype
- Síndrome postfinasterida y disfunción eréctil. Caso clínico y revisión de la literatura
- Approach to Investigation of Hyperandrogenism in a Postmenopausal Woman
- An Approach to the Patient With Hirsutism
- Keratins of the Human Hair Follicle
- The expanding significance of keratin intermediate filaments in normal and diseased epithelia
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- Keratins and disease at a glance
- Coats' Plus: A Progressive Familial Syndrome of Bilateral Coats' Disease, Characteristic Cerebral Calcification, Leukoencephalopathy, Slow Pre- and Post-Natal Linear Growth and Defects of Bone Marrow and Integument
- Shared Phenotypes Among Segmental Progeroid Syndromes Suggest Underlying Pathways of Aging
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- Severe Abnormalities in the Oral Mucosa Induced by Suprabasal Expression of Epidermal Keratin K10 in Transgenic Mice
- Is thyrotropin-releasing hormone a novel neuroendocrine modulator of keratin expression in human skin?
- <i>In vivo</i> alteration of the keratin 17 gene in hair follicles by oligonucleotide‐directed gene targeting
- Alopezien und Hypotrichosen im Kindesalter
- Building Models for Keratin Disorders
- Painful thickened skin on the soles of the feet
- Pioneers in Dermatology and Venereology: An Interview with Professor Danilo V. Stevanovic
- KRT16 wt Allele
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- 559 Visualization of sweat suppression following botulinum toxin A by soluble microneedle arrays
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes