Zobrazeno 1 - 10
of 89
pro vyhledávání: '"V. V. McLaughlin"'
Autor:
Vallerie V. McLaughlin, LJ Rubin, Maurizio Rainisio, David B. Badesch, R.J. Barst, G. Simonneau, Nazzareno Galiè, O. Sitbon, Carol M. Black
Publikováno v:
European Respiratory Journal. 25:942-942
Publikováno v:
European Heart Journal. 43
Background Guidelines for the management of pulmonary arterial hypertension (PAH) recommend early combination therapy of an endothelial receptor antagonist (ERA) and a phosphodiesterase type-5 inhibitor (PDE5i) [1]. There is, however, limited guidanc
Autor:
V. V. McLaughlin
Publikováno v:
European Journal of Clinical Investigation. 36:10-15
Pulmonary arterial hypertension (PAH) is a devastating disease of the small pulmonary arteries and arterioles, characterized by intimal fibrosis, medial hypertrophy and plexiform lesions. When untreated both the idiopathic form (IPAH, formerly termed
Autor:
D, Khanna, Ma, Tan, D E, Furst, N S, Hill, V V, McLaughlin, R M, Silver, V D, Steen, A, Langer, J R, Seibold, Barbara, Segal
Publikováno v:
Clinical and experimental rheumatology. 32(6 Suppl 86)
The aim of this study was to utilise the Quality Enhancement Research Initiative in Systemic Sclerosis (QuERI-SSc) to measure and reduce a perceived gap in the diagnosis of pulmonary arterial hypertension (PAH) associated with systemic sclerosis (SSc
Autor:
V V, McLaughlin, S, Rich
Publikováno v:
The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation. 17(8)
Autor:
V V, McLaughlin, S, Rich
Publikováno v:
Comprehensive therapy. 23(9)
When no other explanation for pulmonary hypertension can be found, it is referred to as primary pulmonary hypertension (PPH). Causes of pulmonary hypertension, with a special focus on PPH, as well as recent advances in both its medical and surgical t
Autor:
V. V. McLaughlin, R. L. Benza, R. J. Barst, V. F. Tapson, Dezheng Huo, Mardi Gomberg-Maitland
Publikováno v:
Journal of Investigative Medicine. 54:S353.4-S353
Purpose The 6-Minute Walk Test (6MW) is the recommended test to assess exercise capacity in pulmonary arterial hypertension (PAH). Metabolic equivalent (MET) is the amount of oxygen used by a seated person and is a predictor of survival in the genera
Publikováno v:
Advances in Pulmonary Hypertension. 2023, Vol. 22 Issue 4, p1-82. 82p.
Publikováno v:
Advances in Pulmonary Hypertension. 2023, Vol. 22 Issue 4, p179-228. 50p.
Autor:
Yao J; School of Life Science and Technology, Key Laboratory of Developmental Genes and Human Disease, Southeast University, Nanjing, China., Zhang Y; School of Life Science and Technology, Key Laboratory of Developmental Genes and Human Disease, Southeast University, Nanjing, China., Wang Z; School of Life Science and Technology, Key Laboratory of Developmental Genes and Human Disease, Southeast University, Nanjing, China., Chen Y; School of Life Science and Technology, Key Laboratory of Developmental Genes and Human Disease, Southeast University, Nanjing, China., Shi X; School of Life Science and Technology, Key Laboratory of Developmental Genes and Human Disease, Southeast University, Nanjing, China.
Publikováno v:
Journal of cellular physiology [J Cell Physiol] 2024 Dec 04. Date of Electronic Publication: 2024 Dec 04.