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Most hospitalized COVID-19 patients had long-term symptoms like fatigue and hair loss, with women and those sicker during hospitalization at higher risk.

The document concludes that while there are various treatments for Alopecia Areata, there is no cure, and individualized treatment plans are essential due to varying effectiveness.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Multiple treatments work best for hair loss.

Research on epidermal stem cells has advanced significantly, showing promise for improved clinical therapies.

Topical latanoprost and bimatoprost eye solutions don't help eyelash growth in people with alopecia areata.

Decomposed tritiated thymidine is less accurate for DNA tracing, and hair changes can indicate malnutrition.

FOXN1 gene variants cause low T cells and immune issues from birth.

Wnt10b makes hair follicles bigger, but DKK1 can reverse this effect.

Bimatoprost, a glaucoma medication, may also help treat hair loss.

Chitosan-decorated polymersomes improve finasteride delivery for hair loss treatment.

Different harmful mutations in the CDH3 gene cause HJMD, but symptoms vary among individuals.

Treating cystoid macular oedema in uveitis is difficult and risky.

The research provides specific measurements for hair follicles that can improve hair transplant and regeneration techniques.

Pitx2 helps outer root sheath cells differentiate but can't start hair growth on its own.

The document explains hair growth and shedding, factors affecting it, and methods to evaluate hair loss, emphasizing the importance of skin biopsy for diagnosis.

Recognizing oral symptoms can help diagnose and treat blood and nutritional diseases early.

Latanoprost can effectively treat eyelash hair loss, with 45% of patients showing hair regrowth and no reported side effects.

Giving docetaxel weekly at 40 mg/m² is manageable and has low toxicity for cancer patients.

Low doses of mixed chemicals cause permanent reproductive malformations in male rats.

Possible new treatments for common hair loss include drugs, stem cells, and improved transplants.

The protein StAR is found in 17 different organs and can affect hair loss and brain functions, but its full role is not yet fully understood.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

Nanoparticulate systems improve drug delivery by controlling release, protecting drugs, changing absorption and distribution, and concentrating drugs in targeted areas.

Improved hair loss treatment using special particles and surfactants.

Premature graying of hair may suggest health issues and currently lacks effective treatments.

Not eating enough protein can cause hair roots to shrink and lose color, and hair to become thinner.

Skin symptoms are important for diagnosing and managing juvenile-onset systemic lupus erythematosus and usually get better with treatment.

Natural 5α-reduced glucocorticoids might be anti-inflammatory with fewer side effects than current options.

Loose anagen hair syndrome, often affecting young girls, can be diagnosed with a hair-pull test and usually gets better on its own, but severe cases may need treatment.