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Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

A specific gene mutation is linked to a hereditary form of dystonia that responds well to certain medications.

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Tofacitinib is a promising treatment for severe alopecia areata, with many patients experiencing complete or partial hair regrowth.

BMP4 gene is crucial for hair follicle development in Liaoning cashmere goats.

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The revised BASP classification for hair loss is less accurate and harder to use but could still be a viable option.

Para-aminobenzoic acid in hair supplements can cause autoimmune hepatitis.

OnabotulinumtoxinA treatment improved hair-pulling disorder and hair regrowth in a woman with chronic migraines.

Temporal triangular alopecia is a harmless, non-progressive hair loss condition.

Ritlecitinib improved hair regrowth and emotional well-being in some alopecia areata patients.

RALF22 is essential for root hair growth in response to fungal emissions in Arabidopsis.

The Intruder is a tool used for safely preparing the area where a donor's tissue is taken.

New RIPK4 gene mutations were found to cause a type of skin and limb birth defect.

A new method allows for controlled, long-lasting delivery of retinoic acid through the skin with less inflammation.

TTD hair is brittle due to fewer sulfur amino acids and unstable disulfide bonds.

A reliable method was developed to measure Minoxidil and Tofacitinib in gel for hair loss treatment.

Ritlecitinib was generally well tolerated in children with alopecia areata.

hsa_circ_0002980 can help stop liver cancer cells from growing and spreading.

The document's conclusion cannot be summarized because the content is not accessible.

Patients with skin cancer on the scalp and ear in Mexico have specific features and results from their treatments.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

Budesonide and N-acetylcysteine reduced tumors and alopecia in mice, regardless of FHIT gene status.