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Research 241–270 of 1000+
- Causality of Aging Hallmarks
- Malignancy and Cancer Treatment-Related Hair and Nail Changes
- Alopecia and Its homoeopathic treatment
- Erythromelanosis Follicularis Faciei et Colli: A Case Report
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- An Atypical Female Case of Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome with Severe Lower Limb Contractures Requiring Orthopedic Surgery
- Oral Presentations
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- MENSTRUAL DISORDERS IN ADOLESCENTS
- Premature graying of hair
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Secondary cicatricial and other permanent alopecias
- Dermatopathology and molecular genetics
- Evolving approaches to profiling the microbiome in skin disease
- Diseases of Periocular Hair
- A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome
- Drug Repurposing Patent Applications July–September 2025
- Genetic Defects of Female Sexual Differentiation
- Muscle pain in a woman with congenital adrenal hyperplasia due to 21-hydroxylase deficiency resolved with testosterone therapy. A case report with 10 years of follow-up
- Hair Shaft Dysplasias
- Premature Hair Graying: Underlying Contributors and Management Approaches - An Updated Literature Review
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Diagnostic approach to low‐renin hypertension
- Disorders of ovulation
- Neuroimaging Findings in Congenital Biotinidase Deficiency: A Case Report
- Syndromes of Severe Insulin Resistance (SSIRs)
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Dermatologic manifestations of endocrine disorders
- Mice with Alopecia, Osteoporosis, and Systemic Amyloidosis Due to Mutation in Zdhhc13, a Gene Coding for Palmitoyl Acyltransferase