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The method accurately measures testosterone metabolites with high sensitivity and low environmental impact.

Rothmund-Thomson syndrome causes skin changes, hair loss, and slightly high lysine and cystine in urine.

Managing recurrent painless thyroiditis is challenging and should be personalized based on episode frequency, severity, symptoms, and patient preferences.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

Testosterone pellets might work for transgender men's hormone therapy, but more research is needed.

Using 5-butylpicolinate esters improves the sensitivity and reliability of detecting testosterone and dihydrotestosterone in saliva.

Hepatitis C and alcohol abuse may lead to porphyria cutanea tarda.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

A new genetic variant in the LIPH gene causes hair growth issues in a Chinese patient.

Hormone therapy for excessive hair growth is as good with GnRHa as with high-dose CPA, but GnRHa has longer-lasting results.

Lichen planopilaris patients are more likely to have hypothyroidism.

PRP with microneedling improves hair growth and patient satisfaction more than injections for androgenetic alopecia.

IFN-γ production by CD4 T cells is crucial for causing alopecia areata.

Troxerutin helps protect skin cells from oxidative stress and may be good for treating hair loss.

TH07 is a topical combination of finasteride, latanoprost, and minoxidil, and shows promise.

Testosterone therapy is effective and safe for women with low sexual desire, but it's hard to access.

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

Trichoscopy is essential for early detection and monitoring of female-pattern hair loss.

Affected males are born with ambiguous genitalia, raised as females, but develop male traits at puberty due to enzyme deficiency.

A hereditary condition causes hair loss and twisted hair in some family members.

Alopecia patients have a higher risk of heart disease.

A Japanese patient with a rare genetic disorder had a less severe case than others, suggesting other factors may affect symptoms.

Prostaglandin D2 increases testosterone production in skin cells through a process involving reactive oxygen species, which could be a new target for treating hair loss and other skin conditions driven by testosterone.

A new method improves platelet testing for heart disease patients.

Overexpressing the Tβ4 gene in goats can increase cashmere production.

Skin cells can help create early hair-like structures in lab cultures.

The study concluded that there is no significant link between thyroid autoimmunity and alopecia areata.

Point of Care in radiology speeds up diagnosis and treatment by performing tests where the patient is.

TTD hair is brittle due to fewer sulfur amino acids and unstable disulfide bonds.

High LH levels cause hair loss by damaging and aging hair follicles.