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Research 151–180 of 1000+
- Recent Updates of the CRISPR/Cas9 Genome Editing System: Novel Approaches to Regulate Its Spatiotemporal Control by Genetic and Physicochemical Strategies
- FOXN1 deficient nude severe combined immunodeficiency
- Case report: Heterozygous mutation in HTRA1 causing typical cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Co-presentation of Tapia's syndrome and pressure alopecia—A rare event after septorhinoplasty: A case report and literature review
- Efficacy and Safety of Sirolimus for Blue Rubber Bleb Nevus Syndrome: A Prospective Study
- O-10 AN OVARIAN THECOMA PRESENTING WITH POST-MENOPAUSAL VIRILIZATION
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Peripheral Arterial Disease: Diagnosis and Management
- Approach to Investigation of Hyperandrogenism in a Postmenopausal Woman
- Trichotillomania
- The clinical management of testosterone replacement therapy in postmenopausal women with hypoactive sexual desire disorder: a review
- Anabolic–Androgenic Steroids and Brain Damage: A Review of Evidence and Medico-Legal Implications
- Mesenchymal stem cell therapy for liver disease: full of chances and challenges
- Morphea: progress to date and the road ahead
- Intradiscal platelet-rich plasma for discogenic low back pain: a prospective cohort study of early clinical outcomes and quantitative MRI findings
- Transcranial Red LED Therapy: A Promising Non-Invasive Treatment to Prevent Age-Related Hippocampal Memory Impairment
- Recent Progress and Morphological Distribution of Polydopamine-Based Biomaterials and Their Applications
- Perspective Chapter: Beyond BMI – Rethinking Obesity Assessment in Women’s Health
- Progressive Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) from a Young Age Due to a Rare Genetic Disorder, Familial Partial Lipodystrophy: A Case Report and Review of the Literature
- A Case of Successful Treatment with Unilateral Oophorectomy in a Patient with Resistant Polycystic Ovary Syndrome
- An N-Ethyl-N-Nitrosourea Induced Corticotropin-Releasing Hormone Promoter Mutation Provides a Mouse Model for Endogenous Glucocorticoid Excess
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- Leydig cell hyperplasia as a cause of virilization in a postmenopausal woman: A case report
- 26-Year-Old Man With New Abdominal Pain
- Glucocorticoids Influencing Wnt/β-Catenin Pathway; Multiple Sites, Heterogeneous Effects
- Pathophysiological Mechanisms in Long COVID: A Mixed Method Systematic Review
- Steroid Cell Tumor of the Ovary in an Adolescent: A Rare Case Report
- Emerging 3D bioprinting applications in plastic surgery
- The significance of the apelinergic system in doxorubicin-induced cardiotoxicity