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Research 901–930 of 1000+
- Syndromes of Severe Insulin Resistance (SSIRs)
- Main Plenary Sessions: Summaries of Papers
- Calcineurin/Nfatc1 signaling links skin stem cell quiescence to hormonal signaling during pregnancy and lactation
- The Significance of Scalp Involvement in Pemphigus: A Literature Review
- What’s New in Facial Hair Transplantation?
- Implications of a Clinically Ignored Site of Acanthosis Nigricans: The Knuckles
- Artificial Intelligence in Patient Education for Androgenetic Alopecia: A Comparative Study of ChatGPT, Gemini, and Deepseek R1
- Hormonal Control of Cardiac Action Potential Phase 1 Currents in the Brugada Syndrome
- THE EFFECT OF HAIR TONIC FROM SECRETOME MESENCHYMAL STEM CELL ON HAIR GROWTH IN HAIR LOSS CASES
- Prematüre Pubarş Olgularının Değerlendirilmesi: Tek Merkez Deneyimi
- Hair loss at 20 associated with prostate cancer risk later in life
- <i>Hedychium spicatum</i>: a systematic review on traditional uses, phytochemistry, pharmacology and future prospectus
- Nonclassic congenital adrenal hyperplasia and the heterozygote carrier
- Epidemiology and burden of alopecia areata: a systematic review
- Hair and scalp disorders
- The Skin and Subcutaneous Tissues
- A conditional multi-trait sequence GWAS discovers pleiotropic candidate genes and variants for sheep wool, skin wrinkle and breech cover traits
- Two novel <i>BTD</i> mutations causing profound biotinidase deficiency in a Chinese patient
- Dynamic Transcriptome Profile Analysis of Mechanisms Related to Melanin Deposition in Chicken Muscle Development
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Identification of Breast Cancer-Associated Lipids in Scalp Hair
- Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome
- Case report: Heterozygous mutation in HTRA1 causing typical cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Identification of Key Pathways and Genes Related to the Development of Hair Follicle Cycle in Cashmere Goats
- Androgenetic alopecia and coronary artery disease in women
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia