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Research 211–240 of 1000+
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Clinical and Genetic Characterization of Tunisian Children with Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets
- Many Paths to Alopecia via Compromised Regeneration of Hair Follicle Stem Cells
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome
- ATP6AP1‐CDG: Follow‐up and female phenotype
- Mast cell hyperplasia in the skin of Dsg4-deficient hypotrichosis mice, which are long-living mutants of lupus-prone mice
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- Shedding light on the FDA’s 510(k) approvals process: low-level laser therapy devices used in the treatment of androgenetic alopecia
- A translational approach to improve therapeutics in atopic dermatitis and beyond
- Tracing the Change and Contribution of Subcutaneous Adipose to Skin Expansion Using a Luciferase-Transgenic Fat Transplantation Model
- Cellular Senescence and Aging in Myotonic Dystrophy
- Congenital cutaneous lymphadenoma
- Surgical treatment of secondary cicatricial alopecia of scalp and eyebrow
- Effect of gelatin nanoparticles’ size and charge on iontophoretic targeted deposition to the hair follicles
- Follicular unit extraction [FUE] – One procedure, many uses
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- Biological therapy in the treatment of melanoma
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Inborn Errors of Metabolism
- A Profile of Advertising in China’s “Socialist-Market Economy”
- Multiscale spatial mapping of cell populations across anatomical sites in healthy human skin and basal cell carcinoma
- Rare Gli1+ perivascular fibroblasts promote skin wound repair
- Editorial: Progress and Prospects on Skin Imaging Technology, Teledermatology and Artificial Intelligence in Dermatology
- THE HUMAN HAIR FOLLICLE PULSATING BIOMAGNETIC FIELD REACH AS POSSIBLE ADDITIONAL FACTOR IN MIGRAINE HEADACHES A BIOPHYSICS BASED HYPOTHESIS
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- Faces of the Face
- Trichosporon asteroides: A novel ethiological agent of Kerion celsi in a child
- Lipedematous alopecia with mucinosis: report of the first case in Taiwan
- Australian Medicines Handbook 2003