Search
for
Sort by
Research 571–600 of 1000+
- 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
- Hair Shaft Defect in a Teenage Girl: Trichoscopy Saves the Day!
- Two females with hair loss
- Gene detection in a family with monilethrix and observation of the treatment effect with 5% topical minoxidil
- Inherited Hairlessness: A Case Study of Familial Congenital Atrichia
- [Wooly hair syndrome. Clinical and microscopic study].
- Keratosis follicularis spinulosa decalvans in a family
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Molecular Genetics of Keratinization Disorders – What’s New About Ichthyosis
- Curly : a new hair defect mutation in the SELH/bc mouse strain
- Keratin 71 Mutations: From Water Dogs to Woolly Hair
- Familial Uncombable Hair Syndrome: Ultrastructural Hair Study and Response to Biotin
- Description of clinical aspects and microscopy of the hair shaft of a carrier of familial monilethrix
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- Familial Cortisol Resistance: Differential Diagnostic and Therapeutic Aspects
- Pili Annulati: A case series and proposal for classification
- Moniletherix
- Novel <i>KRT83</i> and <i>KRT86</i> mutations associated with monilethrix
- Biochemical features of primary cells from a pediatric patient with a gain-of-function <i>ODC1</i> genetic mutation
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Buschke-Ollendorff syndrome