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A comprehensive approach to educating patients and managing side effects is crucial for improving adherence to multiple sclerosis treatments and patient quality of life.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Taking too many vitamin and mineral supplements can cause serious health problems.

Using systemic drugs as creams for skin conditions shows promise, but more research is needed to confirm their effectiveness and safety.

Biotin supplements improved skin and hair problems in a girl with biotinidase deficiency.

Maintain a natural, masculine look while rejuvenating the eye area with careful, tailored techniques.

A new gel form of minoxidil is equally effective for hair growth and safer for the heart and other organs than the traditional solution.

MendelVar is a tool that helps identify important genes by combining GWAS data with Mendelian disease information.

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

Severe acne in a young girl may indicate underlying hormonal issues.

The meeting highlighted the complexity and variability of skin conditions and differing opinions on their diagnoses and treatments.

Early diagnosis and treatment of achalasia and hyperthyroidism improve patient outcomes.

Chemotherapy in children often causes hair loss, nausea, vomiting, and mood swings.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Researchers found a genetic link for hereditary hair loss but need more analysis to identify the exact gene.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

The document is a detailed medical reference on skin and genetic disorders.

Triptolide effectively and safely reduces actinic keratosis lesions in mice.

Cow milk sugars increase fat production and inflammation in skin oil cells.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

The BMP/Smads pathway and Id2 gene control hair follicle stem cells, affecting their rest and growth phases.

Scientists created a tiny, 3D model of a hair follicle that grows and acts like a real one.

The document summarizes medical findings on topics like heart rhythm treatment, sleep apnea therapy, and various health conditions and treatments.

The Hotz-Celsus surgery successfully fixed inward-turning eyelids in cattle.

The twins' condition is unique and doesn't match any known syndromes.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Humans and pets share similar allergy mechanisms, and studying pet allergies can help treat both human and animal allergies.

Certain genetic variations in IL18 may increase the risk of alopecia areata in Koreans.

SLVs help maintain muscle stretch sensitivity and could aid in treating hypertension and muscle spasticity.