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Research 631–660 of 1000+
- Secondary Amenorrhea and Clinical Hyperandrogenism in a 34-Year-Old Female: Polycystic Ovary Syndrome or Not?
- Birth Outcomes of Infants Born to Mothers with Alopecia Areata: A Nationwide Population-based Study in Korea
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- Safety concerns of paternal drug exposure on fertility, pregnancy and offspring: An analysis based on the FDA adverse event reporting system
- What Work-Up Should Be Done for Patients With Alopecia?
- 301 The Spectrum of PLEC Sequence Variants and Related Plectinopathies Including Novel Association with Epidermolysis Bullosa Pruriginosa
- Early Onset Werner Syndrome
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- 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
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- 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?
- Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation
- Canestick Lesion of Vellus Hair in Netherton's Syndrome
- Hair Shaft Dysplasias
- Hair loss and its management in children
- 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
- Bilateral Xen is Used as Minimally Invasive Glaucoma Surgery for Glaucoma in GAPO Syndrome: Case Report