
Hereditary hemorrhagic telangiectasia, or Osler–Weber–Rendu syndrome, is an autosomal dominant vascular disorder that affects multiple systems. It is characterized by skin and mucosal telangiectasias and arteriovenous malformations. In 1876, Sir John Legg described a case of “hemophilia”
Male, Combined Modality Therapy, Risk Assessment, Severity of Illness Index, Pedigree, Survival Rate, Early Diagnosis, Humans, Mass Screening, Female, Telangiectasia, Hereditary Hemorrhagic, Follow-Up Studies, Monitoring, Physiologic
Male, Combined Modality Therapy, Risk Assessment, Severity of Illness Index, Pedigree, Survival Rate, Early Diagnosis, Humans, Mass Screening, Female, Telangiectasia, Hereditary Hemorrhagic, Follow-Up Studies, Monitoring, Physiologic
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 23 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
