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Research 481–510 of 1000+
- The clinicopathological spectrum of trichoepitheliomas: a retrospective descriptive study
- [Congenital hereditary hypotrychosis. Generalized autosomal dominant hypotrichosis with pili torti (hypotrichosis congenita hereditaria Marie Unna)].
- A Clinical Study of Androgenetic Alopecia (III)
- Hypotrichosis with Juvenile Macular Dystrophy in Saudi Arabia: A Case Report
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Coordinated inhibition of SOX9 and cell cycle progression by microRNA-200 restricts sebaceous gland fate specification
- Pancytopenia in epidemic dropsy: a case report
- Association of Baldness with Coronary Artery Disease and Its Severity
- Identification of two novel clusters of ultrahigh-sulfur keratin-associated protein genes on human chromosome 11*1
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- Trichoscopic Features, Clinical Correlates, and Risk Prediction in Female Pattern Hair Loss: A Retrospective Case-Control Study
- Trichoscopic Features, Clinical Correlates, and Risk Prediction in Female Pattern Hair Loss: A Retrospective Case-Control Study
- Biotinidase Enzyme Deficiency ( Case Report )
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Genetics of thyroid lesions updated
- The complex relationship between TFEB transcription factor phosphorylation and subcellular localization
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- The analysis of genetics and associated autoimmune diseases in Chinese vitiligo patients
- Mammalian keratin associated proteins (KRTAPs) subgenomes: disentangling hair diversity and adaptation to terrestrial and aquatic environments
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Novel cosmeceuticals from plants—An industry guided review
- Assessment of copper and zinc status in hair and urine of young women descendants of NIDDM parents
- An incompletely penetrant novel MAFB (p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal osteolysis syndrome
- Autosomal recessive pure hair and nail ectodermal dysplasia linked to chromosome 12p11.1-q14.3 without KRTHB5 gene mutation
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Localization of S100A2, S100A4, S100A6, S100A7, and S100P in the human hair follicle.
- Hereditary vitamin D-resistant rickets in Lebanese patients: the p.R391S and p.H397P variants have different phenotypes
- Next-generation Sequencing Identified a Novel EDA Mutation in a Chinese Pedigree of Hypohidrotic Ectodermal Dysplasia with Hyperplasia of the Sebaceous Glands
- Hair phenotype diversity across Indriidae lemurs
- Inheritance-Specific Dysregulation of Th1- and Th17-Associated Cytokines in Alopecia Areata