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Research 481–510 of 1000+
- How to defeat male pattern alopecia in a trompeur de femmes, who loves to abuse of libido boosters?
- Clinical Application of Classic Prescription in Treating Alopecia
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- Association of Frailty Index with Clinical BPH Progression and Serious Adverse Events: the MTOPS Trial
- Mutation analysis of type II hair keratin gene in a pedigree with monilethrix
- Notes from the Editors Emeritus
- Prodrugs of butyric acid from bench to bedside: Synthetic design, mechanisms of action, and clinical applications
- Acrodermatitis Enteropathica
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability
- Disease causing homozygous variants in the human hairless gene
- 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
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- 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 )
- 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