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First Korean case of Cronkhite-Canada syndrome with colon cancer and serrated adenoma.

The study found a link between the severity of Lichen Planopilaris seen by doctors and the details seen under a microscope, and created a new way to measure this severity.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

Oral lichen planus can appear before lichen planopilaris.

Early scar classification in lupus can improve treatment and patient outcomes.

Enteral supplements can improve symptoms of Cronkhite-Canada syndrome.

Two cases of hairy elbows syndrome were described, with normal skin texture and symmetrical hair growth.

Certain gene variants can influence acne risk and severity.

The patient with severe hirsutism improved after being diagnosed with non-classic congenital adrenal hyperplasia and treated with corticosteroids.

The study concludes that certain domains in Clostridium histolyticum enzymes are structurally unique, bind calcium to become more stable, and play distinct roles in breaking down collagen, with potential applications in medicine and drug delivery.

LGR5 is a common marker of hair follicle stem cells in different animals and is important for hair growth and regeneration.

A new, quick method was developed to analyze skin lipids, discovering a new ceramide subclass.

ARWH is a rare hair disorder with no cure, but potential treatments include minoxidil and other therapies.

The new method is rapid, sensitive, and accurate for evaluating the quality of the medicinal herb Platycladi cacumen.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.

ILC1-like cells can cause alopecia areata by attacking hair follicles.

Hydrophilic carbon dots cause one protein to clump more and prevent another from clumping.

About 13% of women had idiopathic hirsutism and 8.5% had polycystic ovary syndrome in a group of Iranian women.

LSD1 is essential for healthy skin development and creating the skin's protective barrier.

New mutations in the VDR gene cause vitamin D-resistant rickets without hair loss.

Different body areas have unique skin cell communication patterns, explaining why certain skin diseases occur in specific regions.

FCER1A and RGS1 may help diagnose and treat systemic lupus erythematosus.

Lotus corniculatus seed extract reduces oily skin by decreasing sebum production.

Live vaccines can be safely given to infants with a FOXN1 variant if their immune function improves over time.

Chinese patients with primary cicatricial alopecia often have folliculitis decalvans, benefit from treatment, but may experience relapse, with dermoscopy being a useful diagnostic tool.

The document suggests finding a simpler, cheaper way to diagnose Uncombable Hair Syndrome.

Understanding factors affecting recurrence and survival can improve treatment for head and neck skin cancer.

Cutaneous lupus erythematosus is a common skin condition in lupus, affecting mostly young adult females.

Overexpression of Hoxc13 in hair cells causes hair loss and skin issues.