Search

everythinglearnresearchcommunity

for

Search:↓

Metreleptin treatment significantly improved metabolic health in a boy with congenital generalized lipodystrophy.

Sponges made of soy protein and β-chitin with human cells from hair or fat can speed up healing of chronic wounds.

Recognizing unusual brain and skin symptoms is crucial for diagnosing lupus early.

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

LiPADI is a useful tool for monitoring the severity and treatment of lichen planus.

Systemic lupus erythematosus is an autoimmune disease causing diverse symptoms and major organ involvement.

A 5-year-old girl's scalp scarring and hair loss from lupus improved with specific medications.

A Saudi girl was diagnosed with Loose Anagen Hair Syndrome, a rare condition causing easy hair loss without scarring.

Early diagnosis and treatment with corticosteroids can improve outcomes in Cronkhite–Canada syndrome.

High LGR5 levels in glioblastoma indicate poor prognosis and are essential for cancer stem cell survival.

Lichen Planus is a less common condition affecting skin and mucous membranes, with various types and associated risk factors, challenging to diagnose, significantly impacts life quality, and may have a risk of cancerous changes in oral lesions.

The condition might be caused by genetic changes after birth.

A woman with both Cronkhite-Canada syndrome and myelodysplastic syndrome improved significantly with corticosteroid treatment.

Blocking TSLP reduces skin inflammation and cell overgrowth in psoriasis.

PEH in vulvar LS is common and needs careful diagnosis to avoid confusion with cancer.

Stem cell behavior varies with stimuli, and lineage changes can happen without affecting stem cell division.

Discoid Lupus Erythematosus is more common in women aged 31-40, often worsened by sunlight, and confirmed by specific lab tests.

A young man developed a rare, bilateral scalp condition after head trauma, causing hair loss but no neurological or eye issues.

The gene causing hair loss and heart issues in rough coat mice is still unknown.

Combining low-level laser therapy with topical corticosteroids effectively improved Lichen Planopilaris symptoms.

Accurate diagnosis of SLE requires extensive testing due to its complex symptoms.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

Higher activity in lichen planopilaris is linked to certain immune and tissue genes.

Early recognition and management of connective tissue diseases like lupus are crucial in young patients.

Stem cells in the eye have different roles and behaviors, helping maintain and repair the eye's surface.

A semi-automated system can effectively help choose emulsion ingredients, simplifying the creation of medicinal and cosmetic products.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

The muscle damage was caused by T-cell large granular lymphocytic leukemia, not dermatomyositis.

SLE patients experience hair loss similar to telogen effluvium, with hair damage and immune activity at hair follicles.