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Research 481–510 of 1000+
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Extraskeletal actions of vitamin D
- Cutaneous reactions to recombinant cytokine therapy
- 9 Role of 5α-reductase in health and disease
- Beyond Expectations
- The cycling hair follicle as an ideal systems biology research model
- Hair and scalp disorders in ethnic populations
- Gender aspects in skin diseases
- Overview of Facial Plastic Surgery and Current Developments
- Treatment strategies for alopecia
- Black women’s hair: the main scalp dermatoses and aesthetic practices in women of African ethnicity
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Understanding and Management of Female Pattern Alopecia
- Sperm aneuploidy in infertile male patients: a systematic review of the literature
- PTCH1 Germline Mutations and the Basaloid Follicular Hamartoma Values in the Tumor Spectrum of Basal Cell Carcinoma Syndrome (NBCCS)
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Cutaneous features of myotonic dystrophy types 1 and 2: Implication of premature aging and vitamin D homeostasis
- REVIEW OF SO-CALLED ASEPTIC NEUTROPHILIC DERMATOSES
- What′s new in cicatricial alopecia?
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- Cosmetic Surgery in the United States: Its Past and Present
- Significance of iron status in hair loss in women
- Urticaria, Drug Hypersensitivity Rashes, Nodules and Tumors, and Atrophic Diseases
- Hair aging and anti-aging
- Dermatopathology of Common Hair Problems
- Hair Transplantation in the Cicatricial Alopecias
- Trichodystrophies: A hair-raising differential diagnosis
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- Narrative Review of Skin and Pregnancy: Dermatologic Manifestations and Medication Management During Pregnancy
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia