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Research 91–120 of 127
- Androgen Levels and Body Size Are Associated with Directional as Well as Fluctuating Asymmetry Patterns in Adult !Kung San and Kavango Males from Northern Namibia
- Alopecia areata as a paraneoplastic syndrome of Hodgkin’s lymphoma: A case report
- Research Brief: Self-Reports of a Constellation of Persistent Antiandrogenic, Estrogenic, Physical, and Psychological Effects of Finasteride Usage Among Men
- Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)
- Age and Sex-Related Changes to Gene Expression in the Mouse Spinal Cord
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- The sternum reconstruction: Present and future perspectives
- Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention
- Advanced 3D/4D Bioprinting of Flexible Conductive Materials for Regenerative Medicine: From Bioinspired Design to Intelligent Regeneration
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- Faun tail nevus: A series of 15 cases and their management with Intense Pulse Light
- Endocrine abnormalities in ring chromosome 11: a case report and review of the literature
- Matricellular Proteins in the Homeostasis, Regeneration, and Aging of Skin
- Serum Levels of VWF, t-PA, TNF-α, and ICAM-1 in Patients Receiving Hemocoagulase Combined with Platelet-Rich Plasma during Total Hip Replacement
- Alopecia totalis successfully treated with modified platelet-rich plasma therapy in a patient recalcitrant to traditional treatment modalities
- Porokeratotic Eccrine Ostial and Dermal Duct Nevus: A Report of Rare Late-Onset Solitary Lesion
- A guide to diagnosis and management of hypertrichosis
- Mediator 1 ablation induces enamel-to-hair lineage conversion in mice through enhancer dynamics
- Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters
- Case report: Two individuals with AEBP1-related classical-like EDS: Further clinical characterisation and description of novel AEBP1 variants
- Hair loss severity and its impact on quality of life in patients suffering from androgenic alopecia: A one-year cross-sectional study
- A Clinical Genetics-Driven Dual Diagnosis of Prader–Willi Syndrome Due to Mosaic Maternal UPD(15) and NOTCH3-Related CADASIL
- Aesthetic Medicine and Aesthetic Health Psychology: Toward an Integrative Framework for Patient-Centered Care
- A Systematic Scoping Review and Conceptual Analysis of New-Onset Fibromyalgia Manifestations After Non-Hospitalized COVID-19: Empirics, Definitions, Methodologies, Pathophysiology, Mapping of Literature, and Knowledge Gaps
- Linear and Unilateral Basaloid Follicular Hamartoma Along Blaschko’s Lines in an Elderly Patient: A Rare Presentation
- A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome
- Twins with psychiatric features and a nonsense HRAS variant affecting transcript processing
- Bachmann–Bupp syndrome and treatment
- A 15-Year-Old Girl with Trichorhinophalangeal Syndrome Type 1 with Non-ossifying Fibroma in Femur: A Case Report