Outcomes of Childhood Pulmonary Arterial Hypertension in BMPR2 and ALK1 Mutation Carriers

This publication has 29 references indexed in Scilit:

• Missense Mutations of the BMPR1B (ALK6) Gene in Childhood Idiopathic Pulmonary Arterial Hypertension
  Circulation Journal, 2012
• A new nonsense mutation of SMAD8 associated with pulmonary arterial hypertension
  Journal of Medical Genetics, 2009
• Implications of Mutations of Activin Receptor-Like Kinase 1 Gene (ALK1) in Addition to Bone Morphogenetic Protein Receptor II Gene (BMPR2) in Children With Pulmonary Arterial Hypertension
  Circulation Journal, 2008
• Molecular and functional analysis identifies ALK-1 as the predominant cause of pulmonary hypertension related to hereditary haemorrhagic telangiectasia
  Journal of Medical Genetics, 2003
• Primary pulmonary hypertension
  The Lancet, 2003
• Clinical and Molecular Genetic Features of Pulmonary Hypertension in Patients with Hereditary Hemorrhagic Telangiectasia
  New England Journal of Medicine, 2001
• Heterozygous germline mutations in BMPR2, encoding a TGF-β receptor, cause familial primary pulmonary hypertension
  Nature Genetics, 2000
• Familial Primary Pulmonary Hypertension (Gene PPH1) Is Caused by Mutations in the Bone Morphogenetic Protein Receptor–II Gene
  The American Journal of Human Genetics, 2000
• Vasodilator Therapy for Primary Pulmonary Hypertension in Children
  Circulation, 1999
• Survival in Patients with Primary Pulmonary Hypertension
  Annals of Internal Medicine, 1991