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Children with HIV often have skin problems that can indicate the severity of their immune system damage.

Elderly patients frequently suffer from skin conditions, especially inflammatory ones, highlighting the need for better healthcare.

Lichen simplex chronicus on the scalp can be diagnosed by specific hair and skin signs and treated with corticosteroids and therapy.

Zinc sulphate solution was not effective in reducing the number, duration, or severity of recurrent herpes simplex infections.

Acyclovir can prevent rejection of skin grafts in herpes-related lip leucoderma.

Injecting anti-herpes antibodies locally can prevent skin lesions and sweating problems caused by herpes simplex virus in mice.

The specific skin disease variant p.(Arg2000Trp) in plectin can cause a wide range of symptoms, which should be considered when diagnosing patients.

Most HIV-positive patients had skin problems, and conditions like oral thrush and boils were linked to weaker immune systems.

Triple horizontal scalp biopsies are 98% accurate in diagnosing hair loss, better than single biopsies.

Turkish pregnant women commonly experienced skin issues like itching and acne, and doctors mainly used topical treatments due to safety concerns during pregnancy.

Psychotropic medications can cause skin problems but also treat some skin conditions.

Peripilar keratin casts are a helpful sign for diagnosing traction alopecia.

The study found different absorbance values for simplex and complex homoeopathic hair oils when analyzed with a UV-visible spectrophotometer.

Black dots under trichoscopy can appear in different hair and scalp conditions, not just in alopecia areata.

RANKL improves the immune response against herpes simplex virus by enhancing T cell activation and could help develop better treatments or vaccines.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

Skin cells from people with Epidermolysis Bullosa Simplex have abnormally placed and less active mitochondria.

The document explains the genetic causes and characteristics of inherited hair disorders.

Genetic defects and UV radiation cause skin damage and aging.

Microneedle arrays deliver botulinum toxin effectively for sweat suppression, similar to injections.

Scientists found key proteins and genes that affect skin and hair health, and identified potential new treatments for hair loss, skin disorders, and wound healing.

Dandruff is linked to increased T cells and weakened immune protection in hair follicles.

Scientists used stem cells to create a model of the skin disease Epidermolysis Bullosa simplex, which helped them understand its molecular mechanisms and could aid in finding treatments.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

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

Epidermolysis bullosa simplex causes easily blistered skin due to faulty skin cell proteins, leading to new treatment ideas.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Keratin proteins in epithelial cells are dynamic and crucial for cell processes and disease understanding.

Mutations in the LSS gene cause a rare type of hereditary hair loss.