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Using mesenchymal stem cells or their exosomes is safe for COVID-19 patients and helps improve lung healing and oxygen levels.

A rare endocrine disorder, APS 1, was diagnosed in a 26-year-old man in Bangladesh.

Mice treatments didn't grow hair, a patient treatment may affect immune response, and people with hair loss often feel anxious or depressed.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

Bovines can have rare inherited skin diseases with specific symptoms like hair loss, fragile skin, and abnormal porphyrin buildup.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

Early and aggressive treatment is crucial for preserving vision in infants with AEC syndrome.

The book details advanced techniques in cosmetic dermatology for experienced surgeons.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Three related Persian cats have a rare, likely hereditary skin condition causing hair loss and poor coat quality, with limited treatment options.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

The project created a standardized system for classifying skin lesions in lab rats and mice.

Transplant patients often get skin problems, with treatments varying by condition.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Botanical extracts and Minoxidil improved hair condition in a boy with a genetic disorder.

C/EBPalpha and C/EBPbeta are crucial for normal skin and oil gland cell development in adult mice.

A horse in Brazil had seasonal hair loss possibly linked to light exposure and melatonin levels.

Frizzled receptors are essential for various body development processes and maintaining certain body functions.

Interferon alfa-2a is effective for treating cutaneous T cell lymphoma but has significant side effects.

Over half of the children had abnormal hair under a microscope, with many having genetic hair conditions.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

Madarosis is the loss of eyelashes and eyebrows due to various health issues and requires thorough examination to diagnose and treat the underlying cause.

The book provides a historical view of abortion in the U.S., critiques the pro-choice movement, and recommends including abortion in medical education.

Hair loss from Telogen Effluvium can be managed by treating the underlying cause and may improve with treatments like minoxidil.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

Abortion access should be defended on public health grounds, and medical evaluations are crucial in psychiatric cases to avoid misdiagnosis.

Both books are valuable resources in their fields.

The document reviewed various health-related books, focusing on abortion debates, medical conditions, and effective health communication.