Search

everythinglearnresearchcommunity

for

Search:↓

The study found that nerve signals are stronger when there are more connection points, but not necessarily denser, along the nerve's path in the spine.

Botulinum toxin is used for neck, shoulder, calf, and ankle slimming, and hair loss treatment, but can cause muscle weakness and atrophy with regular use.

Neuropsychiatric lupus is a severe form of lupus that needs strong treatment to improve life quality.

THAP1 gene changes do not affect DYT1 dystonia; finasteride may help reduce tics and OCD in Tourette syndrome.

More precise, personalized therapies are needed for autoimmune diseases.

The same genetic mutation in Sjögren-Larsson syndrome can lead to different levels of severity, suggesting other factors influence the symptoms.

A woman's shingles infection triggered her first episode of a rare neurological disorder and blood vessel inflammation.

Spinal fMRI can help understand brainstem and spinal cord function, especially in spinal cord injury patients.

A girl with citrullinemia developed pili torti, suggesting a link between the hair condition and the metabolic disorder.

Mutations in the ACTB gene cause Becker’s nevi and may lead to muscle issues in Becker’s nevus syndrome.

A boy with early puberty and laughing seizures was treated, stopping seizures and slowing puberty.

Early diagnosis and multidisciplinary care, including orthopedic surgery, can prevent long-term disability in IFAP syndrome.

A specific gene mutation causes Olmsted syndrome.

Giant axonal neuropathy changes the structure of keratin in human hair.

Costovertebral arthritis can cause chronic back pain in SLE patients and needs thorough evaluation.

Hair-shaft abnormalities can indicate neurological disorders, some of which are treatable.

Two Hispanic women developed Plica neuropathica, a condition causing tangled hair, possibly due to hair damage and various risk factors.

High-dose testosterone with finasteride improves muscle health in males with spinal cord injury.

Tacrolimus and corticosteroids can improve symptoms of Satoyoshi syndrome.

A woman's hair changed to a dry, tangled texture that's hard to comb after treatment with spironolactone, suggesting the medication might cause such hair changes.

Satoyoshi Syndrome is hard to diagnose and treat due to its rarity and complex symptoms.

The new stiffness test works well for gels but not for sprays.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

PRS injections can improve knee function and reduce pain for up to a year.

Nociplastic type pain, common in Chronic Overlapping Pain Conditions, is a complex, heritable trait linked to 24 unique genetic factors and 127 genes, with potential shared mechanisms in cognitive, personality, and metabolic traits.

Nociplastic pain is a complex, heritable trait with genetic links to chronic and neuropathic pain.

A boy developed a rare skin condition after recovering from a severe skin reaction, and it improved with lotion treatment.

A special receptor in sensory nerve endings helps control how they respond to stretching.

A 17-year-old girl with lupus had vocal cord paralysis but improved with treatment.