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A patient with a nerve disorder died from infection complications after developing insulin resistance from a treatment.

A rare case of Cushing syndrome was successfully treated with one-sided adrenal gland removal, suggesting personalized treatment is important.

Early recognition and treatment of VATS in transplant patients improve outcomes.

People with myotonic dystrophy type 1 have a higher chance of getting skin tumors, including melanoma.

Powered exoskeleton training improves body perception and quality of life in spinal cord injury patients.

A 12-year-old boy in rural south India had a rare skin condition causing hair loss and inability to sweat.

A woman had skin and hair issues after a botulinum toxin injection.

Recognizing eyebrow hair loss linked to a rare skin condition is crucial for proper treatment.

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

Narrowband-UVB phototherapy successfully treated a rare case of Graham Little-Piccardi-Lassueur syndrome.

Men with early-onset hair loss have less cardiometabolic benefit from bromocriptine.

An 8-year-old girl has a rare genetic disorder causing complete, irreversible hair loss and skin bumps.

The Trichodysplasia spinulosa virus protein can cause abnormal hair growth in mice.

Trichoblastomas in aged house musk shrews show unique features and may involve serum amyloid A in inflammation.

Undiagnosed lupus can cause severe complications after epidural anesthesia, leading to muscle weakness and potentially death.

Trichodysplasia spinulosa is a rare skin disease in immunocompromised patients caused by a specific virus targeting hair follicle cells.

Levothyroxine treatment fully cured the young man's hypothyroid symptoms.

Early detection and biotin treatment improve outcomes for biotinidase deficiency.

Consider THPP in patients with muscle weakness and low potassium, as it is often underdiagnosed.

Botulinum A toxin injections reduced pain and promoted hair regrowth in a woman with a rare form of alopecia areata.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

Enobosarm significantly increased muscle mass and improved physical function in elderly men and postmenopausal women without serious side effects.

Children with Parry Romberg Syndrome had successful facial fat-grafting surgeries after disease stabilization with no complications.

A young man was diagnosed with a rare hair loss condition usually seen in older women.

Over-expression of Sp2 can lead to cancer by preventing proper stem cell differentiation.

Parry–Romberg Syndrome can involve the brain even without obvious symptoms, and a new diagnostic framework is suggested for early detection.

Steroid treatment greatly improved the symptoms of a boy with a rare disorder called Satoyoshi syndrome.

Hair regrowth was achieved using 5-Fluorouracil and Bleomycin for scalp atrophy caused by corticosteroids.

Bortezomib chemotherapy can cause temporary skin rashes.