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Coreopsis tinctoria Nutt. extract can effectively dye hair yellow or dark brown with good wash durability.

Calcium supplements improved bone deformities but not skin papules or hair loss.

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

Photothermal biomodulated PRP extends hair graft viability by 2 hours compared to standard solutions.

Chitosan glycolate and lactate sponges are promising for wound healing, while chitosan ascorbate sponges are less effective.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

A new mutation in the mitochondrial DNA was found in a boy with MELAS, even though his family didn't show typical signs.

Treat limited stage small cell lung cancer with chemotherapy and radiation, and consider preventive brain radiation for better survival chances.

Rice bran extract can increase melanin production and may help treat melanin deficiency.

Many survivors of critical illness, especially those with sepsis, experience hair loss.

The new bioreactor improves skin grafts by evenly stretching cells and monitoring conditions for better growth.

Primary mitochondrial cytopathies often cause skin, endocrine, vision, and blood issues, needing careful diagnosis.

A woman was diagnosed with Sheehan's syndrome and a rare complication of diabetes insipidus 33 years after symptoms began, improving with hormone therapy.

Human hair follicles have a unique way of using energy and might use the Cori cycle; blocking CCR5 could help treat hair loss.

Sardinians were historically short due to a mix of genetics and factors like disease and poor nutrition, but recent height increases suggest better living conditions had a bigger impact.

The compounding pharmacy in Venâncio Aires generally follows good practices, with only the Paracetamol sample showing significant microbial growth.

Stopping valproate and using lactulose can quickly treat valproate-induced hyperammonemia.

Recognizing rare causes of MASLD is crucial for effective treatment and preventing complications.

Biotin mega-dose therapy led to dramatic improvement in a newborn with a rare metabolic disorder.

The infant with a urea cycle disorder improved with treatment and a liver transplant.

Liver transplantation is a viable option for children with propionic acidemia, improving quality of life and diet, but does not remove all risks and long-term brain outcomes are uncertain.

Sheep wool follicles can metabolize both glucose and acetate using different pathways important for wool growth.

Minoxidil lowers blood pressure effectively but may cause unwanted hair growth and other side effects.

Necrobiosis lipoidica may need new criteria for accurate diagnosis due to similarities with another condition.

Lambertianic acid helps prevent muscle wasting.

Poly-L-lactic acid injections can cause hair loss and skin issues.

Early diagnosis and treatment are crucial for managing Berardinelli–Seip syndrome.

Correct diagnosis and treatment are crucial for effective management of lipid storage myopathies.

Not having the gene PLAAT3 leads to fat loss, high insulin resistance, and abnormal fat levels in the blood due to a disruption in fat cell development and function.

Lipedematous alopecia causes permanent hair loss due to increased scalp fat.