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Research 271–300 of 1000+
- Androgenic Alopecia Is Associated with Less Dietary Soy, Higher Blood Vanadium and rs1160312 1 Polymorphism in Taiwanese Communities
- Evolving approaches to profiling the microbiome in skin disease
- Common Baldness in Women
- Use of genetics in the prediction of success in male pattern hair loss therapy and mechanistic studies
- Correlation between sebum level and severity of male androgenetic alopecia
- Hair Loss in Children
- Loose anagen hair syndrome in children of Upper Egypt
- Follikelhormone
- Dutasteride Micro-Injections in Androgenetic Alopecia
- Clinico-epidemiology of Keratosis Pilaris with Histopathologic and Dermoscopic Evaluation – A Cross-sectional Study in a Rural Tertiary Hospital
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- Analysis of familial factors using the basic and specific (BASP) classification in Korean patients with androgenetic alopecia
- A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation
- Deciphering the pathogenesis of central centrifugal cicatricial alopecia
- 284 Deciphering the pathogenesis of central centrifugal cicatricial alopecia
- MON-194 A Case Of Sertoli Cell Tumor In A Patient With Familial Partial Lipodystrophy Type 2
- Central centrifugal cicatricial alopecia: challenges and solutions
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Pulmonary manifestations of Birt-Hogg-Dubé syndrome
- CPC14 Blaschko-linear trichoepitheliomas: unveiling type 1 segmental mosaicism
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Dermoscopy: A rapid bedside tool to assess monilethrix
- Osseous Metaplasia and Mature Bone Formation With Extramedullary Hematopoiesis in Trichilemmal Cyst
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- TRPS1 haploinsufficiency results in increased STAT3 and SOX9 mRNA expression in hair follicles in trichorhinophalangeal syndrome
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Causes and Management of Hypertrichosis
- Ectodermal Dysplasia: Variable Expressions
- A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene