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Research 211–240 of 1000+
- Endocrine-skin interactions
- The spectrum of hair loss in patients with mycosis fungoides and Sézary syndrome
- Therapeutic potential of bimatoprost for the treatment of eyebrow hypotrichosis
- Generation of Cashmere Goats Carrying an <i>EDAR</i> Gene Mutant Using CRISPR-Cas9-Mediated Genome Editing
- Epidermal Polarity Genes in Health and Disease
- <i>WNT10A</i> , dermatology and dentistry
- What does acne genetics teach us about disease pathogenesis?
- Hair Loss in Children
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Evaluation of hair loss
- Unruly hair
- Hair loss with levetiracetam in five patients with epilepsy
- Dermatologic manifestations of endocrine disorders
- Common Dermatologic Disorders in Down Syndrome: Systematic Review
- STIM1 R304W in mice causes subgingival hair growth and an increased fraction of trabecular bone
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Hair loss
- White piedra caused by <i>Trichosporon inkin</i> : a report of two cases in a northern climate
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Hair loss in children.
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- Development of squamous cell carcinoma from erythroplasia of Queyrat following photodynamic therapy
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Perturbations in fatty acid metabolism and collagen production infer pathogenicity of a novel MBTPS2 variant in Osteogenesis imperfecta
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- THE GENETICS OF CYP GENE VARIANTS IN ASSOCIATION WITH POLYCYSTIC OVARY SYNDROME: A NARRATIVE REVIEW
- Ritlecitinib in severe alopecia areata: a profile of its use