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Nurses are exposed to chemotherapy drugs, risking health issues like hair loss, so protective gear and monitoring are needed.

Cepharanthine can potentially treat gastric cancer by stopping tumor growth.

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

88% phenol is effective for treating alopecia areata.

Oral difelikefalin significantly reduces itch in notalgia paresthetica.

Early recognition and a team approach are crucial for managing diffuse alveolar hemorrhage in antiphospholipid syndrome.

The method accurately measures cyproterone acetate in plasma, showing no significant difference between two formulations.

Pseudopelade is a rare inherited hair loss condition with a genetic cause.

Cepharanthine is a well-tolerated drug with multiple medical uses, including anti-inflammatory and anti-cancer properties.

Scientists found a new protein, AMY117, common in Alzheimer's patients, which could be important for treatment and diagnosis.

A new molecule was found to be a safe and effective skin lightener and anti-aging product.

Paroxetine relieves pain by increasing allopregnanolone levels.

Poly-L-lactic acid injections can cause hair loss and skin issues.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

DPCP can help regrow hair in some people with severe alopecia.

PTHrP is higher in certain dog tumors and may act as a local growth factor.

Variants in the CCDC47 gene are linked to trichohepatoneurodevelopmental syndrome.

A rare combination of hair loss and excessive fine hair growth was found in celiac disease patients.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

Cadd4 effectively reduces cholesterol levels without side effects.

Valproic acid can cause a rare allergic reaction leading to fluid around the lungs and heart, which is treatable by changing medication.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

Hair dye with para-phenylenediamine can cause skin depigmentation.

The research found how GPCR Class A Rhodopsin receptors are related and suggested possible substances they interact with.

CCC1 is essential for ion balance and proper plant cell function.

A new genetic mutation linked to CARASIL syndrome and small artery disease was found in a Chinese family.

PROTACs offer a new, precise way to treat cancer by breaking down harmful proteins.

Photodynamic therapy successfully treated skin cancer in a 53-year-old woman.

Long-term use of canthaxanthin may cause reversible changes in the eye, including crystal deposits and altered vision responses.