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An 87-year-old man showed unusual signs of Hodgkin lymphoma, primarily high calcium levels, which improved after treatment and revealed the disease.

Hoyeraal-Hreidarsson syndrome in infants causes severe gastrointestinal issues.

Knockout mice showed anemia and hair loss, suggesting other ways exist for iron absorption.

Long-hair follicular unit excision improves hairline restoration results and patient satisfaction.

Hyperaesthetic leucotrichia in horses causes painful, recurring skin lesions and hair color changes, especially in Arabian and American paint horses.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

Intense pulsed light with radiofrequency showed mixed results in improving quality of life for hidradenitis suppurativa patients, with no clinical improvements.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

Mutations in specific genes disrupt development of sweat glands, teeth, hair, skin, and nails in HED.

The Lanceolate hair-J mutation in mice mimics human hair disorders like Netherton's syndrome.

Hair analysis can track haloperidol dosage history.

Mutations in the LIPH gene cause woolly hair in a child.

Er:YAG laser therapy effectively treats Hailey-Hailey disease, leading to long-term remission and improved quality of life.

The mutant HR bmh protein mis-localizes in cells, affecting skin and hair development.

Leuprolide effectively reduces hair growth in hirsute women at higher doses.

The Foxn1(-/-) nude mouse shows disrupted and expanded skin stem cell areas due to high Lhx2 levels.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Hataedock treatment improved skin health and reduced atopic dermatitis symptoms by enhancing the skin barrier and reducing inflammation.

Local testosterone treatment improved sexual desire in a female with fragile X syndrome.

The E413K mutation in the hHb6 gene causes monilethrix, a hair disorder, but doesn't show consistent symptoms.

Hereditary elliptocytosis causes elongated red blood cells and can lead to mild or no symptoms.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

A new method was developed to accurately detect and measure 47 different drug ingredients in various products.

Hexi cashmere goats' hair growth varies by stage, with Hoxc13 linked to hair activity.

Omega-6 fats in certain cells boost male hormone production.

The research confirmed that certain methods are reliable for standardizing Eclipta alba and ensuring its safety and quality in herbal products.

A woman's hair loss and other symptoms were due to a rare hormone deficiency treatable with steroids.

LX-38 is a safer drug option for hair loss and prostate issues without hormonal side effects.