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Probiotics with Lactobacillus reuteri improve IBS symptoms in children.

Pulmonary artery thrombectomy is safe and effective but not widely used.

CAR-T therapy offers hope for children with hard-to-treat blood cancers.

AI improves medical care by enhancing diagnosis and treatment for better patient outcomes.

Patients with limited English prefer professional language interpretation in otolaryngology clinics.

Aortic aneurysm treatment has shifted to less invasive methods, improving safety and outcomes.

The ABI1 gene contributes to prostate cancer progression and treatment resistance.

Cell therapy is advancing with stem cell transplants and genetically modified cells improving treatment for diseases like cancer and autoimmune disorders.

Using Decamethoxine and Blastomunil together speeds up wound healing.

Pre-surgical embolization and a two-stage resection improve outcomes for rare sacral tumors.

Countries should improve sex education, access to contraception, and legal abortion options.

Rhabdomyosarcoma is the most common head and neck cancer in children, requiring complex treatment.

Comprehensive treatment improved hearing in 89.7% of soldiers with blast-induced hearing loss.

Ancient immune and signaling pathways still regulate blood cell development.

Virtual surgical planning improves efficiency, coordination, and precision in complex surgeries.

Local antibiotic therapy can effectively treat root canal infections.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

Terbinafine is the most effective medicine for fungal nail infections, especially for diabetics and those with weak immune systems.

Male infertility and genitourinary birth defects are often linked to genetic issues.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

The meeting highlighted promising genetic treatments for male fertility issues but noted concerns about certain cancer risks and ICSI safety.

H1 increases risk for neurodegenerative diseases, while H2 offers protection but is linked to other disorders.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

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.

TMPRSS2 helps viruses enter cells and protects the prostate from inflammation-related cancer.

Fibroblast bioelectric signaling can promote hair growth and may help treat hair loss.

Stopping finasteride improved sperm counts in two men, reducing the need for fertility treatments.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

Early detection and biotin treatment improve outcomes for biotinidase deficiency.

New genetic mutations linked to rare skin disorders were found in three newborns.