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Taking 100 mg of DHEA daily for 16 weeks did not change metabolic and reproductive health significantly but increased certain ovarian markers with minimal side effects.

Ectodysplasin inhibits Wnt signaling to help form hair follicles.

A man developed severe skin reactions after using a treatment for hair loss.

Predstanormix Duo is a safe and effective new drug for treating urinary symptoms from BPH.

Tissue-engineered skin substitutes can model junctional epidermolysis bullosa and may help develop gene therapy.

New hydrogel dressing with antibiotic speeds up burn healing and skin regeneration.

To improve use of the contraceptive DMPA among adolescents, effectively manage side effects like menstrual changes and weight gain through counseling and guidance.

Taohong Siwu Decoction may help treat deep vein thrombosis by reducing inflammation.

New JAK inhibitor drugs show promise for treating skin diseases but need more research on safety and effectiveness.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Tridax procumbens may help treat diabetes.

Fish skin-derived material helps diabetic wounds heal faster than current options.

The substance DMC helps get rid of aging cells by triggering a process that causes cell death, which could treat age-related diseases.

Mutations in the hairless protein gene cause hair loss.

A 5% concentration of Dorema aucheri extract significantly improves diabetic wound healing.

Polygoni multiflori Radix water extracts promote hair growth in mice.

Wnt/β-catenin signaling is important for keeping skin cell attachment structures stable.

Three compounds from Dadap leaves may help treat hair loss.

Jujube fruit extract may reduce kidney damage from ibuprofen in rats.

The document honored Yvonne, announced upcoming dermatology events, and introduced new journal editors.

DM and AA may share a common cause.

Proper cleansing can resolve dermatosis neglecta, which may indicate underlying psychiatric issues.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

A new method accurately measures molecular movement without complex modeling.