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The combination of Arginine Silicate Inositol Complex and a new form of Biotin improved hair and nail growth in rats.

A man with painful ear plaques was diagnosed with discoid lupus and treated with medications and lifestyle changes.

Dermatopathology has made significant progress but many skin diseases remain incurable, requiring ongoing research.

Ultrasound is a useful, non-invasive tool in dermatology for diagnosing skin conditions and guiding treatments, but it has some limitations.

Sarcoptes mites cause severe skin issues in dogs, which can be fatal if untreated.

Dermal exosomes with miR-218-5p boost hair growth by controlling β-catenin signaling.

In 2002, various drugs caused serious side effects, including vitamin B12 deficiency, heart issues, blindness, hypersexuality, allergic reactions, blood clotting problems, pupil dilation, capillary leak syndrome, muscle breakdown, hepatitis, skin reactions, and lupus.

A new gene location for Keratosis follicularis squamosa was found on chromosome 7p14.3-7p12.1.

PEODDN is a rare skin disorder with limited treatment options, best treated with laser therapy.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

Fat-derived stem cells and their secretions show promise for treating skin aging and hair loss.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

Mice without the vitamin D receptor have bone issues and other health problems, suggesting vitamin D is important for preventing various diseases in humans.

Fluorescence can effectively measure acne treatment progress.

Diagnosing PCOS in teenage girls is tricky and requires careful evaluation and management.

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

Acanthosis nigricans is a skin condition that may indicate a higher risk for insulin resistance and type 2 diabetes, and more research is needed to understand and treat it.

The conclusion is that treatments like finasteride and minoxidil can prevent baldness progression and improve hair density, but more research is needed on other therapies.

The document concludes that early diagnosis and treatment are crucial for managing skin diseases in ferrets.

A possible link exists between minimal change nephrotic syndrome and complete hair loss.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Male pattern hair loss caused by follicular miniaturization; early diagnosis and treatment can reduce psychological burden.

Vitamin D receptor is crucial for starting hair growth after birth.

Hair loss in certain young mice is linked to a specific gene and can be caused by lack of iron.

A gene mutation causes woolly hair in a Syrian patient.

The author now believes tricholemmal carcinoma is a rare type of infundibular squamous cell carcinoma and more research is needed on these tumors.

New treatments for vitiligo may focus on protecting melanocyte stem cells from stress and targeting specific pathways involved in the condition.

Mechanical forces are crucial for shaping cells and forming tissues during development.

The document explains the genetic causes and characteristics of inherited hair disorders.

Stopping infliximab and using strong topical steroids can regrow hair lost due to psoriasiform alopecia.