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Carboplatin-paclitaxel is preferred for advanced lung cancer due to its balance of affordability and patient well-being.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Segmental Vitiligo is a stable, early-onset form of vitiligo that responds well to early treatment and is ideal for repigmentation studies.

Finasteride effectively treats central serous chorioretinopathy.

Genetic variations affect dutasteride treatment response for male pattern hair loss.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

Errors found in identifying furosemide and finasteride polymorphs due to incomplete data.

The two Eclipta alba varieties can be distinguished by their chemical differences.

A reliable method was created to measure dutasteride and related molecules in capsules.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

A pregnant woman with Cushing Syndrome got worse and sadly passed away.

The two finasteride formulations are bioequivalent.

Researchers found a new mutation in the FERMT1 gene in a Spanish family with Kindler syndrome.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

People with keratosis pilaris might be more likely to get a rare type of tinea versicolor.

Severe CCCA may be biologically and clinically different from milder forms.

rwSALT provides precise hair regrowth measurement from scalp photos.

A new type of alopecia areata, called the "confetti variant," causes small bald spots that often heal on their own in a few months.

Trichothiodystrophy is a rare genetic disorder causing hair issues and sometimes linked to DNA repair defects.

A Saudi individual initially identified as a girl had a genetic disorder affecting gender development.

The 2012 criteria are better for diagnosing atypical lupus cases.

A small change in the TRPS1 gene leads to a less severe form of a syndrome affecting hair, nose, and finger development.

CRISPR/Cas9 editing in spinach affects root hair growth by altering specific genes.

Certain gene variations may increase the risk of PCOS in South Indian women.

The new SLICC criteria for diagnosing lupus are more sensitive and accurate than the old criteria.

A specific gene mutation causes varying hair loss severity in a Pakistani family.

A genetic mutation in the hHa1 gene creates a smaller, but still functional, hair protein without causing hair problems.