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Trichoscopy helps tell apart alopecia areata and trichotillomania in Asians by looking at specific hair and scalp features.

The Asian Association of Hair Restoration Surgeons is a group focused on improving hair restoration techniques in Asia.

HDR electronic brachytherapy effectively treats nonmelanoma skin cancer with good cosmetic results and minimal side effects.

Collecting sexual orientation and gender identity data in dermatology can lead to better, more sensitive care for sexual and gender minority patients.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

Key genes and pathways involved in thyroid eye disease were identified, aiding potential treatment and diagnosis.

Certain gene variations might increase the risk of a hair loss condition in Koreans.

Netherton syndrome is a genetic skin disorder causing severe skin issues and requires careful treatment to protect the skin barrier.

EDA2R gene linked to hair loss.

Exosome therapy can safely and effectively restore color to gray hair.

New techniques in hair restoration surgery can fix unnatural results from old methods, improving patient self-esteem.

Early diagnosis and multidisciplinary care are crucial for improving the quality of life in patients with ectodermal dysplasia.

TET enzymes are important for skin and hair development by controlling gene activity in specific areas.

Specific mutations in a receptor cause facial abnormalities and hair loss.

Nestin-expressing hair follicle cells may be useful for nerve repair and regeneration.

The conclusion is that surgeons should carefully create a natural-looking occipital hairline in hair transplants to avoid detection.

Melanocytes are diverse cells important for pigmentation and skin health, influenced by genetics and environment.

Dual TCR Treg cells are common in mouse tissues and vary by location.

Standard reference values for hair analysis in healthy Indian males were established.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

Most patients with hair loss sought treatment for cosmetic reasons, were unhappy about their appearance, and had a family history of the condition, suggesting it may be inherited.

A new AIRE gene mutation causes rare autoimmune symptoms in a Lebanese boy.

Finasteride and CPA-EE2 equally reduce hirsutism, but affect hormone levels differently.

NIH dermatology funding increased by 14.7% from 2015 to 2019, but men and certain states and institutions received most of the money.

Researchers identified genes in scalp hair follicles that may affect hair traits and hair loss.

Women with PCOS are more likely to have impaired glucose tolerance and type 2 diabetes, especially if they are Asian or obese.

Koreans have lower hair density, larger hair diameter, and slower hair growth than Caucasians.

A high neutrophil-to-lymphocyte ratio may predict poor response to hair loss treatment.

A specific DNA region is crucial for Foxn1 gene expression in thymus cells but not in hair follicles.

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