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Research 901–930 of 1000+
- Reliability of the Estimation of the Take of Split Thickness Graft by the Observation Method
- Early-onset Male Androgenetic Alopecia and Metabolic Syndrome: Are They Associated?
- Uncombable hair syndrome: Observations on response to biotin and occurrence in siblings with ectodermal dysplasia
- Monilethrix: A rare hereditary condition
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Ichthyosis hystrix
- Trichothiodystrophy without associated neuroectodermal features in two siblings
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Mesenchymal Stem Cells for the Treatment of Skin Diseases
- Hair follicle stem cells promote epidermal regeneration under expanded condition
- [Translated article] Keys to the Diagnosis of Hair Shaft Disorders: Part II
- Myotonic Dystrophy—A Progeroid Disease?
- Emerging 3D bioprinting applications in plastic surgery
- Variant 1859G→A (Arg620Gln) of the “Hairless” Gene: Absence of Association with Papular Atrichia or Androgenetic Alopecia
- Aberrant Wnt Signaling Induces Comedo-Like Changes in the Murine Upper Hair Follicle
- Moth-eaten alopecia and beyond: Syphilitic alopecia - Revisited
- Isolated patchy heterochromia with pili annulati features on light and electron microscopy
- Clinical Applications of Punch-Based Techniques in Dermatologic Surgery
- Health-related quality of life and mental state in women with polycystic ovary syndrome and migration or minority background – A cross-sectional study
- Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience
- Hair Anomalies in a 6-Year-Old Girl
- Natural Product-Inspired Bis(trifluoromethyl) Phenyl Hydroxycinnamate Derivatives as Promising Nonsteroidal Inhibitors of Human Steroid 5α-Reductase Type-1: Synthesis, <i>In Vitro</i>, and <i>In Silico</i> Studies
- Molecular Genetics of Human Hair Diseases
- TONGUE, RED
- Proteome Analysis of Human Hair Shaft
- Fertility evaluation of infertile women: a committee opinion
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Telogen Effluvium