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Irradiating the whole central nervous system can lead to over 50% of patients with cerebellar medulloblastoma surviving three years.

Autoimmune hepatitis in children often affects girls and can be treated successfully with medication.

Alopecia areata in infants may be more common than previously thought.

The first book is highly recommended for facial surgery education, the second book is useful despite its limited focus, and the third book is not user-friendly due to dense text and poor images.

The Rotterdam Study updated findings on elderly health, focusing on heart disease, genetics, lifestyle effects, and disease understanding.

The Rotterdam Study found risk factors for elderly diseases, links between lifestyle and genetics with health conditions, and aimed to explore new areas like DNA methylation and sensory input effects on brain function.

The Rotterdam Study aims to understand disease causes in the elderly and has found new risk factors and genetic influences on various conditions.

The Rotterdam Study updated its design and objectives in 2012, providing insights into various diseases in the elderly, including skin cancer, bone health, liver disease, neurological and psychiatric conditions, and respiratory issues.

The Rotterdam Study aims to understand various diseases in older adults.

Androgens can both increase and decrease hair growth in different parts of the body.

Radiation therapy with a higher dose for the brain improves survival in cerebellar medulloblastoma.

The document concludes that molluscum contagiosum is a common, benign skin infection in children, often healing without scarring.

Versican, a protein, is less present in thinning hair follicles and this decrease might contribute to common hair loss in men.

Accurate clinical, histological, and genetic methods are key for understanding and treating hair disorders.

Oral minoxidil shows promise in treating monilethrix-related hair loss.

A woman with dermatomyositis showed rare skin symptoms, was treated successfully, and her case suggests checking for cancer in similar patients.

The study concluded that PKP1 is essential for skin integrity and hair growth, and its dysfunction causes the symptoms of ectodermal dysplasia/skin fragility syndrome.

New method measures female hair loss: Female Pattern Hair Loss Severity Index (FPHL-SI).

CD3+ T-cell presence is a reliable marker to tell apart alopecia areata from pattern hair loss.

Researchers created specific antibodies that detect a protein important in development and various conditions, and can be used for research and diagnosis.

Understanding hair follicle structure is key for treating hair disorders and could help develop new treatments.

A woman with a rare type of dermatomyositis improved with low-dose prednisone and methotrexate.

Bariatric surgery is safe and effective for treating adolescent obesity.

Different hair loss types need accurate diagnosis for proper treatment.

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

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Genetics, stress, and health issues can cause early hair greying, which affects self-esteem, and there's no cure, only hair dye.

Humans have limited regenerative abilities, but new evidence shows the adult brain and heart can regenerate, and future treatments may improve this by mimicking stem cell environments.

Terbinafine is the most effective treatment for tinea capitis, a scalp infection often confused with other conditions.

Male hormones may play a role in the development of heart disease, and more research is needed to understand their effects.