Expanding the phenotype of alveolar capillary dysplasia (ACD)
- 30 November 2004
- journal article
- Published by Elsevier BV in The Journal of Pediatrics
- Vol. 145 (5), 646-651
- https://doi.org/10.1016/j.jpeds.2004.06.081
Abstract
No abstract availableKeywords
This publication has 15 references indexed in Scilit:
- BMPR2 Haploinsufficiency as the Inherited Molecular Mechanism for Primary Pulmonary HypertensionAmerican Journal of Human Genetics, 2001
- Molecular mechanisms of development of the gastrointestinal tractDevelopmental Dynamics, 2000
- Familial Primary Pulmonary Hypertension (Gene PPH1) Is Caused by Mutations in the Bone Morphogenetic Protein Receptor–II GeneAmerican Journal of Human Genetics, 2000
- Regulatory molecules in kidney developmentPediatric Nephrology, 2000
- Primary Pulmonary HypertensionNew England Journal of Medicine, 1997
- Misalignment of pulmonary veins with alveolar capillary dysplasia: Affected siblings and variable phenotypic expressionThe Journal of Pediatrics, 1994
- Late presentation of misalignment of lung vessels with alveolar capillary dysplasiaCritical Care Medicine, 1993
- Case 2 Misalignment of Pulmonary Veins and Alveolar Capillary DysplasiaPediatric Pathology, 1991
- Misalignment of lung vessels: A syndrome causing persistent neonatal pulmonary hypertensionHuman Pathology, 1986
- Congenital Alveolar Capillary Dysplasia—An Unusual Cause of Respiratory Distress in the NewbornAmerican Journal of Clinical Pathology, 1981