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Stem cell therapy is promising for treating various health conditions, but more research is needed to understand its full potential and address challenges.

Neurotoxins can affect neurotransmitter release and have potential in treating muscle, pain, and cancer conditions, but more research is needed on how they work.

Multitarget drugs are needed to better treat complex diseases.

Dutasteride may help protect neurons and reduce inflammation in Parkinson's disease.

Bacopa procumbens extract may help protect the brain in Parkinson's disease.

Light therapy on the brain shows promise for treating brain diseases and improving brain function.

Polycystic Ovary Syndrome (PCOS) affects Iranian women's feelings of femininity and self-image.

Scientists found a new protein, AMY117, common in Alzheimer's patients, which could be important for treatment and diagnosis.

If someone has scaly skin, muscle stiffness, and intellectual disability, doctors should consider Sjogren-Larsson Syndrome, but other conditions if more symptoms are present.

Accurate diagnosis of progressive supranuclear palsy requires thorough neurological assessments and MRI.

Hair examination helps diagnose rare neurological diseases in children.

HLD10 can include increased body hair and Mongolian spots.

A girl with hereditary chorea, likely Huntington's disease, had her condition worsened by lupus.

The man has a disease causing skin patches, thickened nerves, and mild muscle weakness.

Alzheimer's patients have higher levels of certain chemicals in their hair.

Dilated pupils can be an early sign of HIV/AIDS.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

Dopaminergic therapy in Parkinson's disease patients is linked to increased hair loss.

Skin issues are common in people with neurodegenerative diseases.

Seborrhea in Parkinson's disease may be linked to hormones, not autonomic impairment.

A baby had a rare condition with abnormal blood vessels in the brain and unusual skin and hair growth, possibly a new syndrome.

A PIK3CA mutation in Schwann cells causes severe nerve damage and increased glycolysis, but early treatment can help.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

Physical inactivity is a primary cause of many human illnesses.

The LMNA mutation affects skin structure even in asymptomatic carriers.

An 11-month-old boy with Menkes disease had severe brain shrinkage and abnormal blood vessels, and didn't respond well to treatment.

Understanding and tracking our body's natural daily rhythms could help improve heart health.

Brain fog in lupus is common, worrying, and often not treated properly.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

The study suggests that motor neurons created from stem cells of patients with spinal and bulbar muscular atrophy show signs of the disease, including changes in protein levels and cell functions.