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Some patients fail bladder function tests due to lower flow rates and higher remaining urine volumes, but the exact reasons for failure are unclear.

IL-17C is important in inflammatory skin diseases and could be a target for treatment.

Lupus pneumonitis can mimic tuberculosis and should be considered in diagnoses.

HS needs personalized treatment plans and more research.

Spermidine may improve skin health and hair growth by enhancing cell function.

Matriptase-2 helps control iron levels by suppressing hepcidin, and its deficiency can cause iron-deficiency anemia.

OCT can effectively diagnose different stages of hair loss non-invasively.

Skin and mucosal issues can occur after COVID-19 in adults and children.

Different S100 proteins have specific roles in various parts of the hair follicle.

Platelet-rich plasma speeds up bone healing and reduces complications.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.

Peanut agglutinin staining helps differentiate malignant melanoma from nevocellular nevus.

The study aims to find the best treatment for central serous chorioretinopathy by comparing various options.

The document concludes that choosing the right biopsy site is crucial for accurate alopecia diagnosis, and combining methods can improve results.

SSEA-4 can distinguish between eccrine and apocrine sweat gland ducts.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Impulsiveness is common across various psychiatric disorders and linked to many psychological symptoms.

The vector successfully directed specific gene expression in hair follicles.

Diagnosing sex development disorders requires combining medical history, physical exams, imaging, lab tests, and genetic data.

The new technique PÂTÉ improved the amount of scalp tissue removed in surgeries.

Social isolation makes mice more sensitive to alcohol's effects on brain function.

ATR-FTIR spectroscopy could help monitor alopecia areata treatment response non-invasively.

Machine learning can help identify biomarkers for personalized Pemphigus vulgaris treatment.

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

Mutations in the SNRPE gene cause hereditary hair loss.

A woman with inflammatory bowel disease improved after treatment with ustekinumab for a rare skin condition associated with her disease.

Sox13 is a marker for early hair follicle development but not essential for skin and hair growth.