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Research 511–540 of 611
- Prevention of Male Late-Onset Hypogonadism by Natural Polyphenolic Antioxidants
- β-Catenin Signaling Evokes Hair Follicle Senescence by Accelerating the Differentiation of Hair Follicle Mesenchymal Progenitors
- Testosterone replacement in 49,XXXXY syndrome: andrological, metabolic and neurological aspects
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Gene-knockout mice with abnormal epidermal and hair follicular development
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Fertility counseling and preservation: considerations for the pediatric endocrinologist
- 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
- A trichobezoar in a child with undiagnosed celiac disease: A case report
- Limb amputations; etiopathogenesis, diagnosis and the multidisciplinary therapeutic approach
- Treatment of Satoyoshi syndrome: a systematic review
- Impact of mTORC1 inhibition on keratinocyte proliferation during skin tumor promotion in wild‐type and BK5.Akt<sup>WT</sup> mice
- Bridging the organoid translational gap: integrating standardization and micropatterning for drug screening in clinical and pharmaceutical medicine
- Hemiagenesis of the thyroid gland detected by coincidence—what is the clinical relevance?
- Is Satoyoshi syndrome an autoimmune disease? A systematic review
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- Cyclosporine-A-Induced Intracranial Thrombotic Complications: Systematic Review and Cases Report
- Porokeratotic eccrine ostial and dermal duct nevus: A noteworthy presentation
- Management of Serious Adverse Events Following Deoxycholic Acid Injection for Submental and Jowl Fat Reduction: A Systematic Review and Management Recommendations
- Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome
- Expression of Signaling Components in Embryonic Eyelid Epithelium
- The dental needs of children with Epidermolysis Bullosa and service delivery: a scoping review
- Mandibulofacial dysostosis with alopecia results from ETAR gain-of-function mutations via allosteric effects on ligand binding
- A Founder Mutation in the <i>POMC</i> 5′-UTR Causes Proopiomelanocortin Deficiency Through Splicing-Mediated Decrease of mRNA
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- ELL Facilitates RNA Polymerase II–Mediated Transcription of Human Epidermal Proliferation Genes
- Remarks on Perfection in Plastic Surgery of the Face
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Severe impact of late diagnosis of congenital adrenal hyperplasia on gender identity, sexual orientation and function: case report and review of the literature