Search

everythinglearnresearchcommunity

for

Search:↓

CD8+ T cells expand significantly in alopecia areata, suggesting new treatment targets.

People living with HIV in Turkey often have skin conditions, which are more common in advanced HIV stages and may help in diagnosing the infection.

Merkel cell carcinoma is most likely to recur within two years of diagnosis, and factors like immune suppression, being over 75, and male sex increase this risk.

Mutation in hairless gene may increase hair loss risk.

A woman's progressive hair loss was correctly diagnosed as a rare condition called fibrosing alopecia in a pattern distribution after initially being mistaken for a more common type.

A rare skin condition caused scarring hair loss on the scalp.

New mutations in the SLC39A4 gene found in twins help understand the genetic cause of acrodermatitis enteropathica.

A mutation in the KRT25 gene causes woolly hair and hair loss.

AHCC reduces hair loss and liver injury caused by chemotherapy in rodents.

People with myotonic dystrophy type 1 have a higher chance of getting skin tumors, including melanoma.

Alopecia areata in these mice is inherited, more common in young females, and can be treated with triamcinolone acetonide.

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

Vogt-Koyanagi syndrome often leads to partial or complete blindness and responds poorly to treatment.

wAMD patients have higher oxidative stress, suggesting antioxidant treatment may help.

A patient's skin rash did not affect the area where a previous viral rash was healing, suggesting a rare immune response.

HMPV causes respiratory infections, mainly managed with supportive care, and lacks a vaccine or specific treatment.

A Japanese patient with a rare genetic disorder had a less severe case than others, suggesting other factors may affect symptoms.

Trichothiodystrophy hair is structurally abnormal with protein and organization issues.

Gonadal hormones significantly affect the severity of alopecia areata in mice.

Trichoscopy effectively diagnoses temporal triangular alopecia in children.

A gene mutation in Lama3 is linked to a common type of hair loss.

Chronic granulomatous disease may be linked to developing systemic lupus erythematosus.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

Antizyme slows skin tumor growth by reducing cell growth in mice.

Combining cell conditioning with mild protease digestion effectively shows versican mRNA in mouse skin sections.

A gene mutation causes monilethrix in a Chinese family.

Topical minoxidil may help treat a rare genetic hair condition with no fully effective treatments yet.

Trichothiodystrophy is a rare genetic disorder causing hair issues and sometimes linked to DNA repair defects.

Hair loss treatment caused more hair loss in a man.