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Research 931–960 of 1000+
- Abstracts
- Clinical Features and Current Therapeutic Approaches to Monilethrix: A Systematic Review
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Hemiagenesis of the thyroid gland detected by coincidence—what is the clinical relevance?
- Eflúvio telógeno após dermatite de contato no couro cabeludo
- Trichonodosis: a case report and literature review
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- A guide to diagnosis and management of hypertrichosis
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- Brief study of hypertrichosis
- Hair Shaft Abnormalities – Clues to Diagnosis and Treatment
- Lichen Planopilaris-Like Changes Arising within an Epidermal Nevus: Does This Case Suggest Clues to the Etiology of Lichen Planopilaris?
- Canestick Lesion of Vellus Hair in Netherton's Syndrome
- Cutaneous Manifestations of Endocrine Disease
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Hepatitis C‐related mixed type vitiligo in a patient with Ivemark syndrome
- Tricorrexis nodosa localizada
- An unusual case of quadruple polyorchidism in a human cadaver mimicking bilateral lipoma
- Delayed Puberty
- P142 – 3046: Encephalocraniocutaneous lipomatosis, a rare neurocutaneous disorder: Report of additional three cases
- Pesticides Exposure and Risk of Hypospadias
- Unruly hair
- Sjogren-Larsson syndrome
- Testosterone replacement in 49,XXXXY syndrome: andrological, metabolic and neurological aspects
- A rare case of woolly hair with unusual associations
- An inherited nail dystrophy principally affecting the great toenails
- Hair loss
- Breast Embryology, Anatomy, and Physiology
- Identification of Somatic <i>KRAS</i> Mutation in a Korean Baby with Nevus Sebaceus Syndrome