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Patients at dermatology specialist hospitals had lower death and readmission rates but higher treatment costs.

The new image descriptor helps identify skin cancer structures with good accuracy.

The HDDPiW-jSB solution may prevent hair loss caused by docetaxel in rats when applied regularly.

A woman's hair loss and other symptoms were due to a rare hormone deficiency treatable with steroids.

High-content screening is useful for finding new treatments for rare diseases and has led to FDA-approved drugs.

Hdac1 and Hdac2 help maintain and protect the cells that control hair growth.

The ProScope HR is an effective, user-friendly, and affordable tool for diagnosing hair loss.

Human hair follicle organ culture is a useful model for hair research with potential for studying hair biology and testing treatments.

Hataedock treatment improved skin health and reduced atopic dermatitis symptoms by enhancing the skin barrier and reducing inflammation.

A specific gene mutation causes sparse, brittle hair in a family.

Mutations in the hairless protein gene cause hair loss.

Researchers made a detailed map of gene activity for different parts of human hair follicles to help create targeted hair disorder treatments.

Diphencyprone treatment increases CD8 lymphocytes in the scalp, which is associated with hair regrowth in alopecia areata patients.

A new genetic mutation in the ODC1 gene causes developmental delay and other symptoms in a young girl.

Inhibiting class I HDACs helps maintain hair growth ability in skin cells.

Digital microscopy can help diagnose hirsutism by measuring hair growth.

A new genetic disorder caused by an ODC1 mutation can be treated with DFMO.

Mice without certain skin proteins had abnormal skin and hair development.

21-hydroxylase deficiency causes hormone imbalances leading to various symptoms, and diagnosis involves clinical and genetic tests.

DVI provides detailed 3D imaging of hair and shows how various products protect and enhance hair.

The enzyme system in hair follicles is similar to the liver's and is affected by certain inhibitors.

Familial dyskeratotic comedones are a rare, benign skin disorder that is hard to treat.

7DHC and BM15766 damage hair follicle structure and reduce key gene expression.

The DNA convention was a valuable opportunity for learning and networking, especially after COVID-19.

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ODAC members faced intense pressure but prioritized scientific evidence in drug approval decisions.

HS needs personalized treatment plans and more research.

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A girl had rickets due to a gene mutation affecting vitamin D response.