Search
for
Sort by
Research 31–60 of 1000+
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Understanding Polycystic Ovary Syndrome
- Alterations in androgen conjugate levels in women and men with alopecia
- The Polycystic Ovary Syndrome - Challenges and Opportunities in Adolescent Medicine
- Wound Healing: A Cellular Perspective
- Pharma in the bedroom . . . and the kitchen. . . . The pharmaceuticalisation of daily life
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Causes of hair loss and the developments in hair rejuvenation
- Genome-wide association study in Japanese females identifies fifteen novel skin-related trait associations
- Lymphatic vessels interact dynamically with the hair follicle stem cell niche during skin regeneration <i>in vivo</i>
- Androgenetic Alopecia: In Vivo Models
- Capitalising on ageing anxieties: Promissory discourse and the creation of an ‘anti-ageing treatment’ market
- Identification of differentially expressed genes in actinic keratosis samples treated with ingenol mebutate gel
- Amyopathic dermatomyositis presenting as severe alopecia and prominent eyelid edema: a case report and literature review
- Autologous Platelet Concentrates in Periodontology : Science, Concept, Protocols and Clinical Applications
- Observations of root hair patterning in soils: Insights from synchrotron-based X-ray computed microtomography
- Elastogenesis Stimulation by Minoxidil or Nebivolol Reduces Premature Aging of the Aortic Wall in Diabetic Mice
- Psychosis as a late manifestation of Sheehan’s syndrome
- Writer’s Cramp Presentation of Woodhouse–Sakati Syndrome – “Out of the Woods”
- Vitamin D Adequacy Conditions the Prolactin-Suppressive Effect of Metformin in Men Receiving Prolactin-Elevating Medications
- Impaired Prolactin-Lowering Effects of Metformin in Women with Polycystic Ovary Syndrome
- Not just thinning: A case of alopecia universalis after mild COVID-19
- Endogenous Skin Fluorescence is a Good Marker for Objective Evaluation of Comedolysis
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Androgenetic alopecia – Current status
- Granulomatous alopecia areata is a valid but rare histologic subset of a common disease
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Adult Male Hypogonadism: A Laboratory Medicine Perspective on Its Diagnosis and Management
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- E-Poster