Search

everythinglearnresearchcommunity

for

Search:↓

Macrophage activation syndrome can be a deadly first sign of systemic lupus erythematosus.

Steroid treatment greatly improved the symptoms of a boy with a rare disorder called Satoyoshi syndrome.

Mitochondrial activity varies in cells before they stop growing, affecting their growth potential.

Alopecia areata involves complex immune responses, suggesting broader treatments could help.

Six key genes can predict bladder cancer outcomes and may serve as prognostic biomarkers.

Anti-Ku-positive patients often have muscle weakness and autophagy plays a key role in their condition.

Leukocyte recruitment is complex but crucial for resolving inflammation and developing effective therapies.

ETC-159 was safe up to 30 mg, but no tumor shrinkage was seen.

A gluten-free diet and removing the parathyroid adenoma helped a girl with coeliac disease and high calcium levels start puberty.

A variant in the KRT31 gene causes a rare hereditary hair disorder called monilethrix.

Early detection of ovarian steroid cell tumors is crucial to prevent lasting symptoms.

Human dermal fibroblasts are the main cells targeted by a virus that can cause a deadly skin cancer, and a certain inhibitor can effectively block this infection.

Monilethrix causes short, fragile hair with no specific treatment available.

SLE can cause unusual gastrointestinal symptoms, and immunosuppressive therapy can be effective.

A rare ovarian tumor was found in a young woman with a genetic fat disorder.

Diagnosing and managing monilethrix is harder when it occurs with other hair loss conditions.

Diagnosing and managing monilethrix is harder when it occurs with other hair loss conditions.

Selenium levels are similar in healthy people from both high and low NPC risk areas.

PCOS is a common hormonal disorder in women, treated with lifestyle changes and hormonal therapy.

LONRF1 is important for oxidative damage response and tissue remodeling during wound healing.

Some hair proteins are specific to hair, while others are also found in skin cells.

The document suggests that there might be an autoimmune link between polycystic ovary syndrome and Graves' disease.

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

MCPIP1 in myeloid cells is important for skin cancer development and healthy hair growth.

The treatment was not recommended due to limited effectiveness and significant side effects.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

CD8+ T cells drive alopecia areata, while regulatory T cells are protective.

A man was diagnosed with a rare form of lupus after showing unique skin symptoms that responded well to treatment.

MITF+ melanoma patients are more likely to have multiple melanomas and unique skin patterns.