Naming and understanding rare diseases: International Classification of Diseases coding and the epidemiologic designations of idiopathic pulmonary arterial hypertension.
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- Type
- letter
- Published
- 2011-03-01
- Cited by
- 3
- References
- 13
- Access
- Open access
- OpenAlex
- https://openalex.org/W2018592189
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:11618210
Keywords
Medicine, Population, Disease, MEDLINE, Orphan drug
References
- Predicting Survival in Pulmonary Arterial Hypertension: Insights From the Registry to Evaluate Early and Long-Term Pulmonary Arterial Hypertension Disease Management (REVEAL)
- Mortality from primary pulmonary hypertension in the United States, 1979-1996.
- Survival in pulmonary arterial hypertension: a reappraisal of the NIH risk stratification equation
- A USA-based registry for pulmonary arterial hypertension: 1982–2006
- Survival in incident and prevalent cohorts of patients with pulmonary arterial hypertension
- An epidemiological study of pulmonary arterial hypertension
- International Classification of Diseases coding changes lead to profound declines in reported idiopathic pulmonary arterial hypertension mortality and hospitalizations: implications for database studies.
- Pulmonary arterial hypertension in France: results from a national registry.
- Pulmonary arterial hypertension: baseline characteristics from the REVEAL Registry.
- Updated clinical classification of pulmonary hypertension.
- Increased mortality in African Americans with idiopathic pulmonary arterial hypertension.
- Pulmonary hypertension surveillance--United States, 1980-2002.
- Surveillance for dental caries, dental sealants, tooth retention, edentulism, and enamel fluorosis : United States, 1988-1994 and 1909-2002