Zobrazeno 1 - 10 of 59 pro vyhledávání: '"A. G. F. Davidson"'
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Burkholderia cepacia in Cystic Fibrosis
Autor: Rita Wittmann, Eshwar Mahenthiralingam, S. Rae, Janet Raboud, Despina D. Frangolias, A. G. F. Davidson, Pearce G. Wilcox
Publikováno v: American Journal of Respiratory and Critical Care Medicine. 160:1572-1577
Variable clinical course has been reported with the acquisition of Burkholderia cepacia in patients who have cystic fibrosis (CF). We hypothesized that the perceived worsening with B. cepacia may reflect the underlying severity of pulmonary disease a
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87e4098b74b3aabf2c75a6982f30b7cd
https://doi.org/10.1164/ajrccm.160.5.9805046
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3
Treatment of recurrent hemoptysis in a child with cystic fibrosis by repeated bronchial artery embolizations and long-term tranexamic acid
Autor: Y. P. Lillquist, A. G. F. Davidson, Gordon Culham, B. P. Dejong, L. T. K. Wong
Publikováno v: Pediatric Pulmonology. 22:275-279
The course of a 12-year-old girl with cystic fibrosis (CF) and with recurrent hemoptysis since age 8 years is described. Conservative measures failed to control her bleeding. Hemoptysis was only partially controlled by repeated bronchial arterial emb
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5ba2d57e0d7e4c367ee326a25ba3ff23
https://doi.org/10.1002/(sici)1099-0496(199610)22:4<275::aid-ppul8>3.0.co
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4
Oral zinc therapy in the treatment of α-mannosidosis
Autor: A. G. F. Davidson, Hilary Vallance, Lawrence T.K. Wong, Derek A. Applegarth, Angela V. Savage
Publikováno v: American Journal of Medical Genetics. 46:410-414
Human α-mannosidosis is a lysosomal storage disorder characterized by mental retardation, dysostosis multiplex, and hepatosplenomegaly. Deficiency of the enzyme leads to accumulation of mannose-rich glycoconjugates in tissues. Zinc sulphate has been
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7097b0ee577214c53f2bfb9965af90c4
https://doi.org/10.1002/ajmg.1320460413
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5
The High Incidence of Valproate Hepatotoxicity in Infants May Relate to Familial Metabolic Defects
Autor: R.E. Appleton, Derek A. Applegarth, A. G. F. Davidson, L. T. K. Wong, J.E. Dimmick, Kevin Farrell
Publikováno v: Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 17:145-148
The incidence of fatal hepatic failure associated with valproic acid (VPA) therapy is highest in children under the age of three years, particularly in those with developmental delay. The pathogenesis of VPA hepatotoxicity is unclear but may relate t
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8b84a2c8a44287c6466658430a62b01
https://doi.org/10.1017/s0317167100030353
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6
The relation of cerebrospinal fluid and plasma glycine levels in propionic acidaemia, a 'ketotic hyperglycinaemia'
Autor: Stanley H. Korman, Peter Heinz-Erian, Daniela Karall, Edda Haberlandt, Y. Lillquist, A. G. F. Davidson, D. A. Applegarth, Sabine Scholl-Bürgi, Jörn Oliver Sass
Publikováno v: Journal of inherited metabolic disease. 31(3)
The characteristic elevation of plasma glycine concentrations observed in propionic acidaemia (PA) and other 'ketotic hyperglycinaemias' has been attributed to secondary inhibition of the hepatic glycine cleavage system (GCS) by accumulating CoA deri
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8de9d4523110a7da52202e1ff8548a3c
https://pubmed.ncbi.nlm.nih.gov/18392751
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7
Role of exercise and nutrition status on bone mineral density in cystic fibrosis
Autor: David L. Kendler, Peter D. Paré, A. G. F. Davidson, Pearce G. Wilcox, Janet Raboud, Despina D. Frangolias, Lawrence Wong
Publikováno v: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society. 2(4)
Background: Exercise has been shown to maintain or increase bone mineral density (BMD) in non-CF populations. Objectives: The purpose of our study was to elucidate the relationship between exercise, body composition and dietary intake with BMD in an
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d1e2eb60290a6da2457224cf1fcc6e6e
https://pubmed.ncbi.nlm.nih.gov/15463867
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9
Selective media for isolation of Burkholderia (Pseudomonas) cepacia from the respiratory secretions of patients with cystic fibrosis
Autor: A. G. F. Davidson, C. Trombley, N. Cimolai, L. T. K. Wong
Publikováno v: Journal of clinical pathology. 48(5)
One hundred and six specimens from 90 patients with cystic fibrosis were evaluated for the presence of Burkholderia cepacia using a current routine diagnostic protocol as well as a research protocol involving polymyxin B-MacConkey agar without crysta
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d480d46ec79b800dad35092ca6bf2b56
https://pubmed.ncbi.nlm.nih.gov/7543119
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10
Pseudomonas aeruginosa colonization of the gastrointestinal tract in patients with cystic fibrosis
Autor: M. E. Campbell, D. P. Speert, A. G. F. Davidson, Lawrence T. K. Wong
Publikováno v: The Journal of infectious diseases. 167(1)
Respiratory and fecal specimens from 111 patients with cystic fibrosis (CF) were cultured on 394 occasions to determine which site Pseudomonas aeruginosa colonizes first. By an enrichment and selection culture technique, P. aeruginosa was recovered f
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d12a55d1396f8f2293df1315364e38c
https://pubmed.ncbi.nlm.nih.gov/8418173
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