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Research 451–480 of 1000+
- Pathophysiology and Nutritional Approaches in Polycystic Ovary Syndrome (PCOS): A Comprehensive Review
- Current Genetics in Hair Diseases
- Acrodermatitis Enteropathica: A Case Report Involving a Delayed Diagnosis
- Polycystic ovary syndrome (PCOS), an inflammatory, systemic, lifestyle endocrinopathy
- Isolation and Characterization of Human Repetin, a Member of the Fused Gene Family of the Epidermal Differentiation Complex
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Novel Compound Heterozygous Variants in the CDC6 Gene in a Russian Patient with Meier-Gorlin Syndrome
- Noval advance of histone modification in inflammatory skin diseases and related treatment methods
- Ichthyosis
- Mutations in ABCB6 Cause Dyschromatosis Universalis Hereditaria
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Ichthyosis linearis circumflexa in a child. Response to narrowband UVB therapy.
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Desmogleins: Hair perspective
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- The Biology and Genomics of Human Hair Follicles: A Focus on Androgenetic Alopecia
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Werner's syndrome: incidental finding during pregnancy
- Prevalence, Symptomatology and Herbal Management of Polycystic Ovarian Syndrome
- APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex
- The Pathogenesis of Primary Cicatricial Alopecias
- Trichoscopy in genetic hair shaft abnormalities
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- A Novel Mouse Type I Intermediate Filament Gene, Keratin 17n (K17n), Exhibits Preferred Expression in Nail Tissue
- FOXP3 <sup>+</sup> regulatory T cells and age‐related diseases
- Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families