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Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

Lichen planopilaris may have a genetic link.

Mutations in Plcd1 and Plcd3 together cause severe hair loss in mice.

LPA3 is crucial for embryo implantation and links LPA to prostaglandin signaling.

Lupus pneumonitis can be misdiagnosed as pneumonia or tuberculosis, so consider lupus in similar cases for proper treatment.

A small group of slow-growing cells causes basal cell carcinoma to return after treatment.

CAL-PDT is safer and more effective for treating actinic keratosis on the scalp.

A patient with a rare form of lupus improved after treatment for skin ulcers and hair loss on the face and scalp.

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

Lidocaine-loaded microparticles effectively relieve pain and fight bacteria in wounds.

Biotin mega-dose therapy led to dramatic improvement in a newborn with a rare metabolic disorder.

PLDζ2 and NPC4 have different roles in lipid changes and root hair growth in Arabidopsis under low phosphate, with PLDζ2 reducing root hair growth and NPC4 promoting it.

KLHL24-mutant stem cells help understand skin and heart disease.

Vitamin D receptor knockout mice have significant motor impairments but no cognitive deficits.

Belimumab reduces disease activity, steroid use, and flares in lupus patients.

The delta lift offers a more natural-looking facelift with fewer side effects.

Diagnosing osteoporosis in transgender people is challenging due to unclear guidelines and hormone treatment effects.

Accurate early diagnosis of Lichen Planopilaris is crucial to prevent permanent hair loss.

Scientists created a cell model to study and find treatments for a skin disease called RDEB.

New therapies for Birt–Hogg–Dubé syndrome are being developed based on understanding the FLCN gene's role.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

Early detection of Lichen Planopilaris is important to prevent worsening and misdiagnosis.

Low-dose naltrexone may help reduce redness in certain scalp conditions.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Finasteride use may be linked to rare testicular tumor, but more research needed.

Pioglitazone may help treat lichen planopilaris, but more research is needed.

The online low-carb program was feasible and acceptable for young women with obesity.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

Researchers developed a new method to find substances in herbs that can block a specific enzyme linked to hair loss.