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Research 91–120 of 1000+
- Neuroendocrine Controls of Keratin Expression in Human Skin
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Diagnostic challenges in determining alopecia areata
- Hair Shafts in Trichoscopy
- Management of congenital ichthyoses: European guidelines of care, part two
- A Practical Approach to the Diagnosis and Management of Hair Loss in Children and Adolescents
- Hairless is a nuclear receptor corepressor essential for skin function
- Hair follicles and their role in skin health
- Darier Sign: A Historical Note
- Oral Presentations
- 15. Hair and Nails
- Dendrobium officinale polysaccharide improves hair regrowth in androgenetic alopecia mice and is associated with coordinated changes in local steroid metabolism, ESR1 activation, and keratin-related follicular responses
- Signaling Involved in Hair Follicle Morphogenesis and Development
- Madarosis, milphosis, eyelash trichomegaly, and dermatochalasis
- Hair Loss in Children
- Alopecia areata: An update
- Acromegaloidism with normal growth hormone secretion associated with X-Tetrasomy
- Acne in Dark Skin
- Clinical Case Notes. Malignant melanoma in eviscerated eyeball
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- Hair Disorders
- Acquired scalp alopecia. Part II: A review
- The endocrinology of baldness
- Low-level light therapy using a helmet-type device for the treatment of androgenetic alopecia
- Transgenic Kallikrein 14 Mice Display Major Hair Shaft Defects Associated with Desmoglein 3 and 4 Degradation, Abnormal Epidermal Differentiation, and IL-36 Signature
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Ovarian steroid cell tumor in a teenager masquerading as polycystic ovary syndrome: a case report and literature review