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Research 901–930 of 1000+
- A novel nonsense CDH3 mutation in hypotrichosis with juvenile macular dystrophy
- Severe Monilethrix Associated with Intractable Scalp Pruritus, Posterior Subcapsular Cataract, Brachiocephaly, and Distinct Facial Features: A New Variant of Monilethrix Syndrome?
- 4 Vitamin D resistance
- Cutaneous immunopathology of androgenetic alopecia
- COVID-19 infection leading to acute pustular dermatoses
- Female pattern hair loss—An update
- Male-pattern baldness and incident coronary heart disease and risk factors in the Heinz Nixdorf Recall Study
- The prevention of benign prostatic hyperplasia (bph)
- Frontal fibrosing alopecia and lichen planopilaris in HLA-identical mother and daughter
- Trichodysplasia Spinulosa: Rare Presentation of Polyomavirus Infection in Immunocompromised Patients
- Alopecia areata with white hair regrowth: case report and review of poliosis
- Association of HSPA1B SNP rs6457452 with Alopecia Areata in the Korean Population
- Syndrome of Birt–Hogg–Dubé, a Histopathological Pitfall With Similarities to Tuberous Sclerosis
- 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
- DNA phenotyping: current application in forensic science
- Intralesional betamethasone as a therapeutic option for alopecia areata
- Hairless Up‐Regulates <i>Tgf‐β2</i> Expression via Down‐Regulation of miR‐31 in the Skin of “Hairpoor” (<i>Hr</i><sup><i>Hp</i></sup>) Mice
- A functional polymorphism in interleukin-1α (IL1A) gene is associated with risk of alopecia areata in Chinese populations
- Inherited Disorders of Corneocyte Proteins
- Single–Follicular-Unit Hair Transplantation to Correct Cleft Lip Moustache Alopecia
- Gene-knockout mice with abnormal epidermal and hair follicular development
- A comprehensive review of the medical and cosmetic applications of exosomes in dermatology
- Longitudinal Assessment of the Prevalence of Actinic Keratosis and Extensive Risk Factor Evaluation: An Update from the Rotterdam Study
- The Complexity of the Ovine and Caprine Keratin-Associated Protein Genes
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Analysis of pediatric dermatology inpatient consultations in a pediatric teaching hospital
- Lamellar ichthyosis with pseudoexon activation in the transglutaminase 1 gene
- Hair Care and Dyeing
- Hair Manifestations of Systemic Disease