Zobrazeno 1 - 10 of 58 pro vyhledávání: '"S G Haworth"'
1
Risk of cardiac catheterization under anaesthesia in children with pulmonary hypertension
Autor: C. J. Taylor, S. G. Haworth, Graham Derrick, M. R. J. Sury, A. McEwan
Publikováno v: British Journal of Anaesthesia. 98:657-661
Background Children with primary pulmonary hypertension (PHT) are a high‐risk group who require assessment by cardiac catheterization under anaesthesia. Complications, including death, have occurred during anaesthesia in these patients, but the tru
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5f98603cec83038d336cffa8d75294b
https://doi.org/10.1093/bja/aem059
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3
Vasoconstriction of intrapulmonary arteries to P2-receptor nucleotides in normal and pulmonary hypertensive newborn piglets
Autor: Geoffrey Burnstock, M R McMillan, S G Haworth
Publikováno v: British Journal of Pharmacology. 128:549-555
1. The vasoconstrictor responses of isolated intrapulmonary arteries (IPA) to P2-receptor agonists was investigated during adaptation to extrauterine life in the normal piglet and the effect of pulmonary hypertension was studied following exposure of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::dc76a7fc8aabaefa36caf7f3f3d1a935
https://doi.org/10.1038/sj.bjp.0702814
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4
Resting potentials and potassium currents during development of pulmonary artery smooth muscle cells
Autor: Alison M. Gurney, S. G. Haworth, O. N. Osipenko, A. M. Evans
Publikováno v: American Journal of Physiology-Heart and Circulatory Physiology. 275:H887-H899
The pulmonary circulation changes rapidly at birth to adapt to extrauterine life. The neonate is at high risk of developing pulmonary hypertension, a common cause being perinatal hypoxia. Smooth muscle K+ channels have been implicated in hypoxic pulm
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0c756ca57033d827e7df210db59cad4d
https://doi.org/10.1152/ajpheart.1998.275.3.h887
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5
Effect of cold preservation on pulmonary arterial smooth muscle cells
Autor: S. M. Hall, S. G. Haworth
Publikováno v: American Journal of Physiology-Lung Cellular and Molecular Physiology. 270:L435-L445
The efficacy of preservation fluids on the cytoskeleton and contractile function of porcine pulmonary arterial smooth muscle (SM) cells during cooling and rewarming was evaluated, using EuroCollins solution (EC), University of Wisconsin solution (UW)
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfdac105905fd5122517c0e114e3c25d
https://doi.org/10.1152/ajplung.1996.270.3.l435
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7
Severe pulmonary vascular occlusive disease following bone marrow transplantation in Omenn syndrome
Autor: S. G. Haworth, W. Permanetter, R. J. Haas, Bernd H. Belohradsky, R. Roos, C. Brückmann, W. Lindner
Publikováno v: European Journal of Pediatrics. 150:242-245
A 5-month-old infant presented with severe combined immunodeficiency disease, reticuloendotheliosis, and hypereosinophilia (Omenn syndrome) resulting in recurrent infections and endomyocardial disease. Bone marrow transplantation from an HLA-identica
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ff2283a88f8031241b31cc28296c658
https://doi.org/10.1007/bf01955521
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8
Kawasaki disease: echocardiographic features in 91 cases presenting in the United Kingdom
Autor: M J Dillon, S G Haworth, A Suzuki, V Gooch, E J Tizard
Publikováno v: Archives of Disease in Childhood. 65:1142-1146
Ninety-one patients with Kawasaki disease were examined by cross sectional echocardiography between 1980 and 1988. In the 75 patients evaluated during the acute phase of the illness (the first month), the first echocardiographic examination was carri
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b73e20b299b94fa4eaf005588192b7c4
https://doi.org/10.1136/adc.65.10.1142
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9
Early-life pulmonary arterial hypertension with subsequent development of diffuse pulmonary arteriovenous malformations in hereditary haemorrhagic telangiectasia type 1
Autor: Helmut Popper, S G Haworth, A Gamillscheg, C J Mache
Publikováno v: Thorax. 63(1)
The case history is presented of a male infant who was thought to have idiopathic pulmonary arterial hypertension (PAH) at 3 months of age. Subsequently the PAH decreased unexpectedly and diffuse pulmonary arteriovenous malformations (PAVMs) were see
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21e33faa782fdb09f251bd69ab8c08fc
https://pubmed.ncbi.nlm.nih.gov/18156574
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10
Sildenafil in neonatal pulmonary hypertension due to impaired alveolarisation and plexiform pulmonary arteriopathy
Autor: Jon Smith, M Vogel, S G Haworth, C Wright, Milind Chaudhari
Publikováno v: Archives of disease in childhood. Fetal and neonatal edition. 90(6)
We report a case of severe pulmonary hypertension in a neonate associated with impaired alveolarisation and plexiform pulmonary arteriopathy. Treatment with oral sildenafil in addition to inhaled nitric oxide (NO) resulted in recovery from the pulmon
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::396fc438c301c42db1491d9d3838d2e8
https://pubmed.ncbi.nlm.nih.gov/16244212
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