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Polarizing light microscopy can easily and reliably diagnose congenital keratinizing disorders like Netherton syndrome.

UTMD with diclofenac and Doxil® improves cancer treatment by boosting immune response and reducing tumor-supporting cells.

Trichoscopy can diagnose Netherton syndrome without pulling hairs.

Nephronectin is linked to worse breast cancer outcomes and helps cancer spread.

Diamond nanoparticles can penetrate skin and reach hair follicles, useful for imaging applications.

Netherton syndrome causes specific skin and hair changes that help in early diagnosis.

A deep learning model was developed to help diagnose trichothiodystrophy by analyzing hair patterns.

An intact skin barrier is crucial to prevent infection in cases of tether-induced tenosynovitis.

Electron Beam Tomography (EBT) is a useful additional test to stress testing for detecting heart disease.

NIR-II imaging effectively tracked stem cells that helped repair facial nerve defects in rats.

Proactive monitoring and management are essential to maximize the benefits of Trastuzumab Deruxtecan while minimizing serious side effects.

Using DNase enzymes to break down harmful NETs could be a new treatment for Stevens-Johnson syndrome and toxic epidermal necrolysis.

ATR12-351 ointment safely delivers LEKTI protein to the skin, reducing enzyme activity in Netherton syndrome.

Doctors should consider Netherton syndrome in patients with chronic skin and hair issues to avoid misdiagnosis.

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

Trichoscopy is useful for diagnosing Netherton syndrome in children with skin issues.

Hydroxychloroquine effectively treated twenty-nail dystrophy in a patient with alopecia areata.

The DNN-DTIs method accurately predicts drug-target interactions and is useful for drug repositioning.

The NUDT15 R139C variant causes thiopurine-induced leukocytopenia through a different mechanism than previously thought in Japanese patients with inflammatory bowel disease.

Trichorrhexis nodosa is mainly caused by hair trauma and improves with gentler hair care.

Early diagnosis and a multidisciplinary approach are crucial for children with Trichothiodystrophy and hidden learning disorders.

Iron deficiency anemia can cause hair breakage.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Tattooing helps treat skin conditions, reconstruct nipple-areola, mark radiation fields, and locate lesions.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

Genotyping for NUDT15 p.Arg139Cys can help predict thiopurine side effects in Japanese IBD patients.

NB-002 is a promising new topical treatment for fungal nail infections, showing better results than a non-medicated option.

The nanocrystalline suspension effectively delivers dutasteride over time with minimal inflammation.

The NUDT15 gene variant causes severe side effects from azathioprine in some Indian patients.