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The summit aimed to speed up finding treatments for alopecia areata.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

Azathioprine can cause severe blood issues and hair loss, needing careful monitoring and possible discontinuation.

Swedish men with the E213 A-allele of the androgen receptor have a lower risk of prostate cancer.

Mice with a changed Hr gene lose and regrow hair due to changes in the gene's activity.

Genetic mutations can affect female sexual development, requiring personalized medical care.

A gene mutation worsens skin irritation in mice due to a lack of certain fats.

There is no significant link between alopecia areata and the PON1 enzyme polymorphisms studied.

A certain gene variation is linked to a higher risk of polycystic ovarian syndrome in South Indian women.

HNG may help prevent the negative effects of chemotherapy on sperm production and white blood cell counts.

Men with early balding should be checked for metabolic syndrome, as there's a link between the two.

Gene mutations can cause problems in male genital development.

Living near more dermatologists and using certain cancer screening tests lowers the chance of being diagnosed with advanced skin cancer.

The number of new cases of cutaneous B-cell lymphoma has leveled off since the early 2000s, and survival rates have improved since 1973.

Psoriasis increases annual healthcare costs by $4,044 per patient, with biologic treatments costing significantly more than phototherapy.

The document concludes that various medications and treatments can have significant, sometimes adverse, effects on health outcomes.

Blood tests for tumor cells could improve prostate cancer diagnosis and treatment; hair loss severity linked to a gene affecting prostate conditions.

The document concludes that a new biosensor can efficiently detect prostate cancer cells and that standardized referrals help find significant cancers effectively.

CEC levels may be a useful marker for predicting prostate cancer progression.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.

Parthenolide promotes hair growth in mice and may influence pathways related to male pattern baldness.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

Melatonin directly affects mouse hair follicles and may influence hair growth.

Mice treatments didn't grow hair, a patient treatment may affect immune response, and people with hair loss often feel anxious or depressed.

Some skin conditions are associated with other serious diseases, and office microscopy may miss many fungal infections.

The conclusion is that many small genetic variations influence claw disorders in cows, and using genomic selection could help reduce these disorders.

Scientists created MUSIi010-A, a stem cell line from a balding man's scalp, to study hair loss and develop potential treatments.

Gene variation affects prostate issues and hair loss.

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

Finasteride dosages should be adjusted based on CYP3A5 genotype and liver function to avoid side effects.