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Permanent hair loss after a stem cell transplant can be a sign of chronic immune system attack on the scalp.

HAIRCARECUBE TM (HCC) helps hair products work better by getting active ingredients deeper into the hair.

Most HIV patients in the study showed skin and mucous membrane issues, with oral thrush being the most common.

NKG2D gene polymorphism doesn't affect SLE risk but may influence symptoms like rash and hair loss.

Tenofovir is more effective than adefovir for resistant hepatitis B, Fibroscan is good for assessing liver damage, regulatory T cells may help hepatitis C persist, and other insights into liver health and disease were found.

A new tool helps study hair follicle cells to develop better treatments for hair disorders.

cGVHD often severely affects the skin, causing rapid aging and other issues.

Different body parts have varying levels of certain hair follicle markers.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

A patient developed a blister at the injection site after hepatitis C treatment.

Visceral leishmaniasis can mimic rheumatoid arthritis symptoms, especially in immunocompromised patients.

Clq deficiency is linked to systemic lupus erythematosus symptoms.

An 87-year-old man showed unusual signs of Hodgkin lymphoma, primarily high calcium levels, which improved after treatment and revealed the disease.

Modulating the BTNL2 pathway can prevent hair loss in mice.

Scarring alopecia involves increased immune cells and specific gene changes near damaged hair follicles.

Hodgkin's lymphoma can show up as hair loss.

Certain genes may be linked to autoimmune conditions in people with alopecia areata.

A new skin cancer can develop where shingles once occurred.

A specific gene variant (rs4833095) is linked to a higher risk of alopecia areata in Koreans.

Higher levels of certain immune cells in hair follicles may contribute to alopecia areata.

Three characteristics of plasmacytoid dendritic cells help tell apart lupus-related hair loss from LPP.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

Alopecia areata is linked to immune system differences, with specific biomarkers like CXCL9 and CXCL10 being key for diagnosis and potential treatment targets.

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

New and known mutations in the hairless gene cause a hair loss condition called Atrichia with papular lesions.

IL-17 plays a key role in severe hair loss in chronic alopecia areata.

A specific gene variant is linked to a higher risk of hair loss from chemotherapy in breast cancer patients.

TCHHL1 is a protein important for hair growth, found in hair follicles.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.