Search

everythinglearnresearchcommunity

for

Search:↓

All parts of the CLASI-A score are important for assessing skin activity in cutaneous lupus erythematosus.

New LPP subtype affects vellus hairs, mimics AGA, and needs biopsy for diagnosis.

Different connective tissue disorders have unique symptoms and treatments, with varying outcomes and often require ongoing care from a specialist.

New LPA receptors (LPA4, LPA5, LPA6) have diverse roles in the body.

A rare lupus case on the chin was successfully treated with steroids and immunomodulators after accurate diagnosis using advanced imaging techniques.

The new assay can track and measure melanosome transfer between skin cells, confirming filopodia's role in this process.

Exosomes from Pinctada martensii mucus can safely reduce melanin production, offering a new treatment for skin pigment issues.

The CLASI is a reliable tool for measuring the severity of cutaneous lupus erythematosus.

Tjalma Syndrome is a rare condition in people with lupus, causing fluid buildup and high CA-125 levels, but not due to tumors.

The method effectively detects banned substances in urine for sports antidoping.

Lichen planus pigmentosus and fibrosing frontal alopecia in Colombia are likely different stages of the same disease.

LPR1 regulates root growth under low phosphate stress independently of SIZ1 in Arabidopsis thaliana.

Mesenchymal stem cells and their secretome may offer a safe and effective treatment for systemic lupus erythematosus.

Sunscreen spray on the scalp may be linked to a type of scarring hair loss.

Early and aggressive treatment with individualized care plans is crucial for managing pediatric systemic lupus erythematosus.

Effective treatments for lichen planopilaris are unclear due to inconsistent results and a lack of strong research evidence.

The PON1 192R gene variant is linked to a higher risk of psoriasis and heart disease in Western Mexico.

Lichen Planopilaris causes irreversible hair loss due to immune attacks on hair stem cells, but modulating PPAR-γ might help treat it.

Laminin-511 may contribute to psoriasis by affecting skin cell growth and survival.

Spironolactone, a heart and liver drug, has new uses including cancer treatment, viral infection prevention, and skin condition improvement.

Hairless protein reduces Msx2 gene activity, affecting hair follicle development.

An infant with Hutchinson-Gilford Progeria Syndrome had successful surgery to fix breathing issues caused by a new genetic mutation.

The long-pulsed alexandrite laser is effective for hair reduction, particularly for light-skinned individuals with dark hair, but caution is needed for darker skin.

Triple therapy with clobetasol, hydroxychloroquine, and N-acetylcysteine is recommended for better outcomes in treating lichen planopilaris.

Lichen planopilaris can cause hair loss on limbs, not just the scalp.

A child had a rare case of scarring hair loss with skin disease, which is hard to treat and stressful.

Early diagnosis and treatment of Lichen Planopilaris are crucial to prevent permanent hair loss.

The SLICK1 allele in Holstein heifers affects hair and immune traits without altering prolactin signaling.

A child's rare skin disease was triggered by chickenpox.

A 30-year-old man with rare skin conditions improved with antibiotics and surgery, hinting at a link to rosacea.