Disease: Hemangiomatosis- familial pulmonary capillary
- A 24-Year-Old Woman With Dyspnea, Chest Pain, and Dry Cough
- A 63-Year-Old Woman With Neurofibromatosis Type 1 and Pulmonary Hypertension With Worsening Hypoxemia
- A founder EIF2AK4 mutation causes an aggressive form of pulmonary arterial hypertension in Iberian Gypsies
- Capillary hemangiomatosis like-lesions in lung biopsies from children with congenital heart defects
- Clinical phenotypes and outcomes of heritable and sporadic pulmonary veno-occlusive disease: a population-based study
- Diagnosis and classification of pulmonary hypertension
- Different sizes of centrilobular ground-glass opacities in chest high-resolution computed tomography of patients with pulmonary veno-occlusive disease and patients with pulmonary capillary hemangiomatosis
- Dual-energy CT lung perfusion characteristics in pulmonary arterial hypertension (PAH) and pulmonary veno-occlusive disease and/or pulmonary capillary hemangiomatosis (PVOD/PCH): preliminary experience in 63 patients
- EIF2AK4 mutations in pulmonary capillary hemangiomatosis
- Endothelin receptor antagonists for pulmonary arterial hypertension
- Familial pulmonary capillary hemangiomatosis early in life
- Familial pulmonary capillary hemangiomatosis resulting in primary pulmonary hypertension
- Functional validation of EIF2AK4 (GCN2) missense variants associated with pulmonary arterial hypertension
- Genetic analyses in a cohort of 191 pulmonary arterial hypertension patients
- Genetics of Pulmonary Arterial Hypertension
- Genetics of pulmonary hypertension
- Genetics of pulmonary hypertension in the clinic
- Heritable pulmonary hypertension: from bench to bedside
- Lung ventilation/perfusion scintigraphy in pulmonary capillary hemangiomatosis: a pattern to consider
- Molecular mechanisms of pulmonary vascular development
- Natural History over 8 Years of Pulmonary Vascular Disease in a Patient Carrying Biallelic EIF2AK4 Mutations
- Novel EIF2AK4 mutations in histologically proven pulmonary capillary hemangiomatosis and hereditary pulmonary arterial hypertension
- Pulmonary capillary haemangiomatosis causing pulmonary arterial hypertension: a clinician's conundrum
- Pulmonary capillary haemangiomatosis: a rare cause of pulmonary hypertension
- Pulmonary Capillary Hemangiomatosis and Pulmonary Veno-occlusive Disease
- Pulmonary Capillary Hemangiomatosis as a Rare Underlying Cause of Primary Pulmonary Hypertension: A Case Report in an Adolescent
- Pulmonary capillary hemangiomatosis: a case series and review of literature
- Pulmonary capillary hemangiomatosis: a focus on the EIF2AK4 mutation in onset and pathogenesis
- Pulmonary hypertension and right ventricular failure. Part VI. Classification and pathomorphology of primary pulmonary arterial hypertension
- Pulmonary hypertension presenting with apnea, cyanosis, and failure to thrive in a young child
- Pulmonary veno-occlusive disease
- United States Pulmonary Hypertension Scientific Registry: Baseline Characteristics
- Update on the pathomorphological assessment of vasculopathies in pulmonary arterial hypertension
- Updated clinical classification of pulmonary hypertension
- Vascular Ehlers-Danlos syndrome with cryptorchidism, recurrent pneumothorax, and pulmonary capillary hemangiomatosis-like foci: A case report
- Widening the landscape of heritable pulmonary hypertension mutations in paediatric and adult cases