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Patients with chronic graft-versus-host disease often have skin problems like vitiligo and alopecia areata.

HLA can be linked to autoimmune hepatitis.

The girl had harmless hair casts, not lice.

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

Padina arborescens and its component MOGG may help prevent hair loss through several actions, including blocking a hair loss-related enzyme.

Ethyl glucuronide levels in hair can change when exposed to artificial sunlight, depending on hair color and thickness.

A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

The microenvironment affects the behavior and survival of melanocytes with the GNAQ oncogene in melanoma.

A woman in Sri Lanka was diagnosed with lupus after presenting with protein loss from the gut and other symptoms.

Atypical symptoms in lupus can indicate different kidney issues.

Lichen spinulosus, usually seen in young people, can rarely occur in adults, as shown by a 52-year-old woman with a rough, bumpy rash.

Cheonggukjang may help prevent and manage various diseases and improve overall health, but its odor and safety concerns need addressing.

GMG-43AC may help reduce unwanted hair growth and treat certain hair loss conditions.

Allopurinol may cause rare granulomatous microscopic colitis.

Ruxolitinib may help treat hair loss and symptoms in patients with chronic graft-versus-host disease.

Netherton Syndrome is a non-treatable genetic disorder in children causing skin, hair, and allergy issues.

The 5/G hydrogel effectively improves diabetic wound healing.

Lipopolysaccharides boost wheat seedling growth, but procyanidin B2 weakens this effect.

ILC1-like cells can cause alopecia areata by themselves.

The role of γδT-cells in causing alopecia areata remains unclear.

Most patients experienced mild to moderate skin problems during a trial for a desmoid tumor treatment.

A woman experienced severe side effects from a drug due to a specific genetic variation, suggesting genetic testing could prevent such risks.

LncRNA MTC boosts growth of goat skin cells, improving cashmere quality.

Laminin-511 is involved in psoriasis development and can be regulated by cannabinoid receptor type 1.

The LMNA mutation affects skin structure even in asymptomatic carriers.

Patients with one autoimmune disease should be checked for other autoimmune disorders.

Alopecia areata may protect against graft dysfunction, while asthma may increase its risk.