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Standardized kits improve the quality and consistency of isolating stem cells from fat tissue.

Simvastatin may help manage symptoms in women with non-classic congenital adrenal hyperplasia by lowering cholesterol and certain hormone levels.

The case suggests a possible autoimmune link between lichen sclerosus and vitiligo.

A woman with CCCA has hair loss due to factors like straighteners and tight hairstyles, and treatments include steroids and avoiding certain hair products.

A woman with anorexia improved significantly after being treated for scurvy with vitamin C, despite not showing typical scurvy symptoms.

Targeting TCR-Vβ2 in cutaneous T cell lymphoma shows promise for safer, more specific treatment.

Cancer-associated fibroblasts promote tumor growth in skin cancer.

Cronkhite-Canada syndrome may be more treatable and less severe than previously thought.

Using cidofovir cream for a rare skin disease can cause skin darkening.

D-OCT shows increased blood vessel growth in response to tissue damage in Frontal Fibrosing Alopecia and is useful for diagnosis and monitoring.

Drug repositioning offers hope for new, affordable treatments for a genetic skin disorder called ARCI.

The virus linked to a rare disease was found in a patient's blood and urine before skin symptoms appeared.

Anabolic-androgenic steroid abuse can cause heart damage and sudden death.

General surgeons in India need to manage peripheral arterial disease due to a shortage of vascular surgeons.

C3G and Vitisin A may help prevent hair loss by blocking male hormones and stopping hair cell death.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

Clouston syndrome can lead to skin cancer, so monitoring is crucial.

A preauricular crease is common in people with coronary artery disease.

Skin stem cells were turned into heart cells using a chemical, suggesting a new way to treat heart attacks.

Two siblings with a genetic mutation had a form of rickets that doesn't respond to vitamin D.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

A 21-year-old male has a rare scalp condition with excessive skin folds.

Some families have a genetic condition where they are born with irregular scalp defects.

SAD patients show different brain activity patterns, which might help identify the disorder.

The vitamin D receptor is essential for skin stem cells to grow, move, and become different cell types needed for skin healing.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

NISCH syndrome is a rare genetic disorder affecting skin and liver, with variable symptoms and limited treatment options.