Search Results - "Urquhart, D.S."

Clinical interpretation of cardiopulmonary exercise testing in cystic fibrosis and implications for exercise counselling by Urquhart, D.S, Vendrusculo, F.M

“…Summary The measurement of exercise capacity in persons with cystic fibrosis by Cardiopulmonary Exercise Testing (CPET) offers a functional assessment of lung…”
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Respiratory Complications in Children with Prader Willi Syndrome by Tan, H.-L, Urquhart, D.S

“…Summary Prader Willi syndrome, resulting from the partial deletion or lack of expression of a region of genes on the paternal chromosome 15, has a number of…”
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233 Three-year experience of a new clinic dedicated to the care of screened infants with equivocal CF related diagnosis by Fall, A.J, Urquhart, D.S

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WS04.6 Airway clearance physiotherapy can reduce dead space and lead to improvements in ventilatory inhomogeniety during exercise in patients with cystic fibrosis: a pilot study by Vendrusculo, F.M, Johnstone, Z, Dhouieb, E, Donadio, M.V.F, Cunningham, S, Urquhart, D.S

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WS08.6 Cardiopulmonary exercise testing provides additional prognostic information in people with cystic fibrosis by Hebestreit, H, Hulzebos, E, Schneiderman, J, Karila, C, Boas, S, Kriemler, S, Dwyer, T, Sahlberg, M, Urquhart, D.S, Lands, L, Ratjen, F, Takken, T, Varanistkaya, L, Rücker, V, Hebestreit, A, Radtke, T

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283 Evaluation of a novel behavioural intervention programme (BIP) to modify mealtime behaviour for young children with cystic fibrosis by Coates, A.J, Harte, C, Urquhart, D.S

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EPS4.02 Earlier identification of cystic fibrosis diabetes in children with cystic fibrosis – real-world experience on the use of continuous (flash) glucose monitoring by Coates, A.J., Chelminska, M., Urquhart, D.S.

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Postmortem brain MRI with selective tissue biopsy as an adjunct to autopsy following neonatal encephalopathy by Nicholl, R.M, Balasubramaniam, V.P, Urquhart, D.S, Sellathurai, N, Rutherford, M.A

“…Abstract Following the death of a neonate it is essential that parents are given full and accurate information about the probable cause of death. Perinatal…”
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P472 Exercise education for professionals in cystic fibrosis: an international journal club by Tomlinson, O.W., Williams, C.A., Urquhart, D.S., Radtke, T.

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P039 Changes to clinical well-being following initiation of elexacaftor/tezacaftor/ivacaftor in children with cystic fibrosis – single-centre experience by McGrath, A., Dowle, H., Marwick, J., Tennant, E., Urquhart, D.S.

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P036 Exercise performance before and after introduction of elexacaftor/tezacaftor/ivacaftor (Kaftrio®) in Scottish children with cystic fibrosis: a 2-centre retrospective study by Burns, P.D., Urquhart, D.S., Blacklock, S., Langley, R.J., Davies, P.L.

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ePS2.10 Exercise testing and training in cystic fibrosis clinics in the United Kingdom: a 10-year update by Tomlinson, O.W., Williams, C.A., Saynor, Z.L., Stevens, D., Urquhart, D.S.

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P051 Real-world experience of change in lung clearance index (LCI2.5) following initiation of elexacaftor/tezacaftor/ivacaftor in children with cystic fibrosis aged 6 through 11 by Dowle, H., Gilchrist, T., Moffat, K., Forster, J., Macleod, K.A., Urquhart, D.S.

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Exercise testing in cystic fibrosis: Who and why? by Urquhart, D.S., Saynor, Z.L.

“…Annual review exercise testing is recommended by the Cystic Fibrosis (CF) Trust. Testing to date has focused on evaluating aerobic fitness, a key prognostic…”
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An innovative strategy for personalised medicine in a CFSPID case that evolved with time by Twynam-Perkins, J., Fall, A., Lefferts, J.W., Urquhart, D.S.

“…We present a challenging case that illustrates how the clinical manifestations in children with CFTR mutations of uncertain significance may change over time…”
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P118 Real-world impact of elexacaftor/tezacaftor/ivacaftor on quality of life of children with cystic fibrosis aged 6–11 years and primary caregivers in the UK: MAGNIFY, a prospective, observational, non-interventional study by Thia, L.P., Thursfield, R., Lee, T., Legg, J., Maitra, A., Urquhart, D.S., McKinnon, C., Lu, M., Liu, J., Jennings, M., Vega-Hernandez, G.

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WS01.02 The current state of play regarding exercise testing in cystic fibrosis: co-development with the community by Saynor, Z.L., Gruet, M., McNarry, M.A., Button, B., Morrison, L., Wagner, M., Sawyer, A., Hebestreit, H., Stanford, G.E., Radtke, T., Urquhart, D.S.

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Pre-operative respiratory assessment for children with spinal deformity by Prentice, K.M., Tsirikos, A.I., Urquhart, D.S.

“…Pre-operative respiratory assessment of children with spinal deformity requires an understanding of the deformity, the proposed surgery and most importantly…”
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WS14.03 Cystic Fibrosis-Related Diabetes is not associated with maximal aerobic exercise capacity in cystic fibrosis (CF): a cross-sectional analysis of an international multicentre trial (ACTIVATE-CF) by Radtke, T., Kriemler, S., Stein, L., Karila, C., Urquhart, D.S, Orenstein, D.M, Lands, L.C, Schindler, C., Eber, E., Haile, S.R, Hebestreit, H.

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WS04.6 Effects of a partially supervised conditioning program in cystic fibrosis: an international multi-centre, randomised controlled trial (ACTIVATE-CF) by Hebestreit, H., Kriemler, S., Schindler, C., Stein, L., Karila, C., Urquhart, D.S., Orenstein, D.M., Lands, L., Schaeff, J., Radtke, T.

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