Search

everythinglearnresearchcommunity

for

Search:↓

A woman with childhood growth hormone deficiency had multiple hormone deficiencies and developed serious lung and kidney problems later in life.

Using buccal mucosa for hypospadias repair in children is effective and reduces complications.

Hidradenitis suppurativa tunnels have different microenvironments, suggesting targeted treatments could be more effective.

A new tool helps study hair follicle cells to develop better treatments for hair disorders.

Age-related hair loss is linked to the decline and dysfunction of hair follicle stem cells.

Botulinum toxin type A injections may help treat hidradenitis suppurativa.

Woodhouse-Sakati syndrome can cause writer's cramp and other varied symptoms, highlighting the importance of genetic testing for diagnosis.

Rehabilitation improved patients' mobility but did not reduce 30-day hospital readmission rates after stem cell transplants.

Diagnosing both systemic lupus and hemoglobinopathy is challenging due to overlapping symptoms.

BMI is a simple, cost-effective tool for screening obesity and related diseases.

Hypoxic preconditioning helps human hair follicle stem cells survive oxidative stress.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

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

Treatment improved symptoms in a woman with HAIR-AN syndrome.

Two patients had a unique form of trichothiodystrophy with reduced high-sulfur proteins in their hair.

The document suggests treating individuals with nonclassic congenital adrenal hyperplasia who show symptoms, especially those related to excess male hormones.

HtrA2 activity is crucial for normal hair growth by regulating fat cell development.

Researchers found key regions in the mouse hairless gene that control its activity in skin and brain cells, affecting hair follicle function.

Research on Hutchinson-Gilford progeria syndrome could help understand normal aging and heart disease.

Overexpressing NSD3 in mice causes breast cancer-like tumors and gland abnormalities.

Tunisian children with hereditary vitamin D-resistant rickets showed improvement with calcium treatment, and new genetic mutations were identified.

Scientists used stem cells to create a model of the skin disease Epidermolysis Bullosa simplex, which helped them understand its molecular mechanisms and could aid in finding treatments.

Dihydrotestosterone changes some hormone-related gene expressions in rat pituitary glands but doesn't affect the estrous cycle.

The conclusion is that hirsutism should be diagnosed and treated because it affects quality of life and may signal other health problems.

Hidradenitis suppurativa tunnels have different microenvironments, suggesting targeted treatments could be more effective.

Hidradenitis suppurativa tunnels have different microenvironments, suggesting targeted treatments could be more effective.

A rare gene mutation causes skin fragility and itching without affecting hair or nails.

Most Recessive Dystrophic Epidermolysis Bullosa patients with a specific mutation likely have Sephardic ancestry from about 500 years ago.

A unique gene mutation causes vitamin D-resistant rickets without causing hair loss.