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The document concludes that most hair loss treatments don't work, balding isn't caused by dandruff, and hair loss may indicate serious health issues that require medical attention.

Chemotherapy in the first trimester of pregnancy is risky, but in the second and third trimesters, it's generally safe with careful drug selection and timing.

Certain proteins, Lgr5 and Lgr6, are important markers of adult stem cells and are involved in tissue repair and cancer development.

K_ATP channel gene mutations are linked to heart diseases, but more research is needed to understand the connection and treatment potential.

The niche environment controls stem cell behavior and plasticity, which is important for tissue health and repair.

Hormonal therapies are safe and effective for treating adult women's acne.

Common acne treatments can cause various side effects, like skin irritation and more serious issues, but combination therapies are often more effective and better tolerated.

Skin and hair can help us understand organ regeneration, especially how certain stem cells might be used to form new organs.

The document concludes that inherited epidermolysis bullosa is a challenging genetic condition requiring multidisciplinary care and new treatments.

Researchers found a safe and effective way to pick genetically modified skin cells with high growth potential using CD24.

The document concludes that eyelash trichomegaly, which is the abnormal growth of eyelashes, can be present from birth, caused by diseases, or result from certain medications.

The document suggests that certain protein deficiencies and scalp blistering in Epidermolysis Bullosa may cause hair loss.

A young woman's Cronkhite-Canada syndrome improved on its own after she gave birth.

Cantú syndrome may be linked to pituitary adenomas.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Extra virgin olive oil may boost the immune system and help fight infections like COVID-19.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

Biomedical engineers are crucial for developing better treatments for chronic and autoimmune diseases.

A 37-year-old male with severe skin and internal issues has a rare inherited skin condition called dystrophic epidermolysis bullosa.

The document is a detailed guide on skin conditions and treatments for dermatologists.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

Proper care and diet are crucial to prevent health issues in gerbils.

The document suggests a bacteria plays a significant role in acne rosacea and that white hair can regain color after transplant, meriting more research on reversing grey hair.

Atopic dermatitis may have genetic causes and can be treated with pharmacologic methods, glycerin creams, and controlling Staphylococcus aureus colonization.

Prurigo pigmentosa mainly affects middle-aged White and Asian women, often linked to a ketogenic diet, and is best treated with oral antibiotics.

A 15-year-old girl has a skin condition causing blisters on her feet, likely inherited from her family.

Knocking out certain genes in mice helps understand skin and hair growth problems.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Key genes crucial for sheep hair follicle development were identified, aiding fine wool breeding and human hair loss research.