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A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

A new pain-measuring system using sensors and AI can effectively detect pain in mice, which may help assess pain in humans and develop treatments.

Defective repair processes may cause immune activation and inflammation in psoriatic disease.

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

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

A skin condition called pyodermatitis vegetans was found in a patient with multiple myeloma for the first time.

Certain skin conditions may indicate or increase the risk of Parkinson's disease.

The document suggests doctors should watch for bone marrow suppression and severe hair loss in patients treated with Azathioprine.

Neuroendocrine paraneoplastic syndromes often show skin changes, helping early diagnosis and requiring a team approach for best care.

Hair glycation can indicate long-term blood sugar levels and diabetic nerve issues.

A new imaging method helps see and study touch nerve endings in mouse skin.

The patient's hair had unique damage and a lower sulfur-to-nitrogen ratio compared to relatives, but not compared to healthy controls.

A woman with Parry-Romberg syndrome developed new curly hair on one side of her scalp, a condition not previously linked to the syndrome.

Patients with pernio have lower vitamin B12 and ferritin levels than healthy people.

Myasthenia gravis can affect both motor and non-motor systems due to immune system issues.

Early recognition and multidisciplinary management are crucial for improving outcomes in Parry-Romberg syndrome.

Plica neuropathica can occur with diffuse alopecia and should be considered in diagnosis.

Insulin helps heal corneal wounds and nerves in diabetic mice by activating the Wnt signaling pathway.

Neuropilin 2 may be a biomarker for melanoma and affects melanocyte behavior.

Long COVID affects over half of COVID-19 survivors, causing a range of symptoms like fatigue and neurological issues, with no specific treatment yet.

A man developed neurological issues from SARS-CoV-2 without severe breathing problems, worsening to death.

A new genetic mutation in the TRPV3 gene causes Olmsted-like syndrome in a Mongolian family.

Azathioprine can help with relapses and disability in NMOSD but has more side effects and needs more research.

A special treatment speeds up chronic wound healing by fixing cell energy issues and reversing aging in cells.

Sensory neuron and Merkel cell changes in the skin happen independently during normal skin maintenance.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Merkel cells stabilize nerve endings in the skin, and they change independently of each other.

A potential genetic link between Werner syndrome and kidney disease was suggested.

Increasing neurotrophin 4 in skin boosts nerve endings but not sensory neuron count.