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A mutation in the HR gene causes a rare form of irreversible hair loss in two Kashmiri families. Whole exome sequencing is effective for finding such mutations.

A man with a rare lung-focused form of hypereosinophilic syndrome improved with steroid treatment.

HLA-DRB5 and other genes may be linked to alopecia universalis.

Amyloid deposits linked to a type of protein may cause a unique pattern of hair loss by disrupting hair growth cycles.

The patient had a severe allergic reaction to gold treatment.

Amphetamine use may not cause hair loss, "geezer" traits are normal aging, not all educated older people are stereotypes, and metronidazole can rarely cause lung disease.

A gene mutation causes lanceolate hair in rats by disrupting hair shaft integrity.

The mouse model showed defects in adult stem cell maintenance related to Hutchinson-Gilford progeria syndrome.

EGFR inhibitors can cause unusual localized hair growth.

The report shows a young man with Hutchinson-Gilford Progeria Syndrome had typical and additional eye problems related to the disease.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

Removing the liver tumor improved the patient's skin condition and hair growth.

Vogt-Koyanagi syndrome often leads to partial or complete blindness and responds poorly to treatment.

Sympathetic activation and venous tone are crucial for heart failure symptoms.

Glucocorticoid treatment improved symptoms in a girl with Satoyoshi disease.

Screening for iron levels in patients with hair loss may help find a genetic iron overload condition early.

A rare genetic mutation caused severe symptoms in a 6-year-old girl with mandibuloacral dysplasia type A.

The document concludes that treatment improved skin lesions but not scalp hair loss in two patients with Graham-Little-Piccardi-Lassueur syndrome.

Granulomatous Alopecia Areata is rare and may be caused by hair antigens or follicle destruction.

Thymoma-associated multiorgan autoimmunity can cause liver damage and affects multiple organs, with limited treatment options and a generally poor prognosis.

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

Regulatory measures are needed to ensure safe production and use of platelet concentrates in Brazil.

Community pharmacies and pharmacists play a crucial role in improving community health.

Older age, obesity, hirsutism, and having children increase metabolic risk in women with PCOS.

Defective mitochondrial DNA replication causes aging symptoms and increased oxidative damage in mice.

Researchers found a new genetic mutation causing a rare hair loss condition in the first Japanese child studied.

An 80-year-old man grew extra hair on his forearms after starting Alzheimer's medication rivastigmine.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

A specific gene mutation causes sparse, brittle hair in a family.