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Activating Nrf2 can help protect against hearing loss.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Early treatment of mixed connective tissue disease is crucial to prevent severe autoimmune conditions.

Low Level Laser Therapy may improve noise-induced hearing loss.

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.

4-octyl itaconate may prevent hearing loss caused by the drug cisplatin by activating certain cell protection pathways.

Fibrinogen/LDL apheresis may improve speech perception in sudden hearing loss, especially for those with high fibrinogen and LDL levels.

Mutations in the PTPRQ gene cause significant balance issues in mice due to hair bundle defects in the inner ear.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

The book details skin conditions in older adults, their link to mental health, cancer treatment importance, hair loss remedies, and managing autoimmune and itchy skin.

Many patients experience long-lasting symptoms like fatigue and pain after COVID-19, regardless of initial disease severity.

COVID-19 leaves 80% of patients with long-term symptoms like fatigue and headaches.

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

The document suggests using natural remedies like bloodletting and honey for various health issues but lacks scientific evidence for their effectiveness.

The document concludes that Borrelia afzelii causes a skin condition in France, a gene is linked to hair loss in Caucasian women, and various genetic mutations affect skin diseases.

COVID-19 can cause over 50 long-term symptoms, with fatigue and headache being the most common.

Animal models, especially mice, are essential for advancing hair loss research and treatment.

Harlequin mutant mice have hair loss due to low AIF protein levels and retroviral element activity.

The document concludes that managing skin conditions during pregnancy is important and requires specialized care.

The NAMS 2014 recommendations guide healthcare providers on treating health issues in midlife women, emphasizing individualized care and informed decision-making.

A mutation in the EDNRA gene causes Oro-Oto-Cardiac syndrome, affecting face and heart development.

DN106212, an extract from a plant, is better at promoting hair growth than other tested substances by affecting hair growth factors and follicle development.

Effective management of children's hair loss involves accurate diagnosis, various treatments, and supportive care.

New treatments for hair loss may target specific pathways and generate new hair follicles.

Increasing Rps14 helps grow more inner ear cells and repair hearing cells in baby mice.

Botanical extracts and Minoxidil improved hair condition in a boy with a genetic disorder.

The new method makes it easier to study the whole cochlea from newborn mice and rats in the lab.

Woodhouse-Sakati syndrome often causes sexual development issues, hair loss, learning disabilities, deafness, muscle contractions, limb pain, and diabetes.

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.