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Research 91–120 of 1000+
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- Genetic correlation by pedigree analysis in patients diagnosed with PCOS as per Rotterdam’s criteria
- Sparse Brittle Hair and Bilateral Temporal Alopecia in a Child
- Dermoscopic Features of Pili Annulati: Features of PA
- Woolly hair generalizado: caso clínico e revisão da literatura
- Hypotrichosis and Hair Loss on the Occipital Scalp
- Moniletrix. Observación de esta infrecuente displasia pilosa en dos hermanos. Reporte clínico y dermatoscópico
- Monilethrix – Case report of a rare disease
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- Monilethrix with Acitretin
- Informàtica i Dret penal: Els delictes relatius a la informàtica
- A University Center for the Performing Arts
- Spatiotemporal secondary hair follicle development in the Lanyu pig (Sus scrofa taivanus): a novel pelage hair follicle model
- A Case Report of Kaphaja Granthi w.s.r. to Trichilemmal Cyst
- Alopecia frontal fibrosante: revisão bibliográfica dos aspectos gerais, fisiopatológicos, diagnósticos e do tratamento
- ST Premature Graying Hair in Seven Years Old Children
- The Role of rs6152 Allele and Non-Genetic Factors in Androgenetic Alopecia: A Pilot Study in the Indonesian Local Population
- P378: Expanding the phenotype of hyper-IgE syndrome: Heterozygous VUS in IL6ST with elevated serum IgE and isolated abscesses
- Pearly Pinna Papules in a Young Female
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- Coexistence of Woolly Hair and Monilethrix: A Cases Study
- Clinical and molecular genetic studies in hereditary hair loss
- Hair Shaft Defect in a Teenage Girl: Trichoscopy Saves the Day!
- Two females with hair loss
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Gene detection in a family with monilethrix and observation of the treatment effect with 5% topical minoxidil
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- [Wooly hair syndrome. Clinical and microscopic study].