Early detection of cystic fibrosis lung disease: multiple-breath washout versus raised volume tests

…, J Stroobant, A Wade, C Wallis, H Wyatt… - Thorax, 2007 - thorax.bmj.com
Background: Lung clearance index (LCI), a measure of ventilation inhomogeneity derived
from the multiple-breath inert gas washout (MBW) technique, has been shown to detect …

Lung function is abnormal in 3-month-old infants with cystic fibrosis diagnosed by newborn screening

…, KL Costeloe, J Price, A Shankar, C Wallis, HA Wyatt… - Thorax, 2012 - thorax.bmj.com
Background Long-term benefits of newborn screening (NBS) for cystic fibrosis (CF) have
been established with respect to nutritional status, but effects on pulmonary health remain …

[BOOK][B] Audio post production for television and film: an introduction to technology and techniques

H Wyatt, T Amyes - 2013 - api.taylorfrancis.com
… Copyright © 2005, Hilary Wyatt and Tim Amyes. The right of Hilary Wyatt and Tim Amyes to
be identified as the authors of this work has been asserted in accordance with the Copyright, …

[HTML][HTML] Parents' experiences of receiving the initial positive newborn screening (NBS) result for cystic fibrosis and sickle cell disease

…, S O'Driscoll, K Johnson, D Rees, H Wyatt… - Journal of genetic …, 2016 - Springer
The clinical advantages of the newborn screening programme (NBS) in the UK are well
described in the literature. However, there has been little exploration of the psychosocial impact …

Relative ability of full and partial forced expiratory maneuvers to identify diminished airway function in infants with cystic fibrosis

…, J Stroobant, A Wade, C Wallis, H Wyatt… - American journal of …, 2002 - atsjournals.org
The tidal and raised volume rapid thoracoabdominal compression techniques are increasingly
used to detect diminished airway function in infancy. The aim of this study was to assess …

[HTML][HTML] Prevalence of nontuberculous mycobacteria in cystic fibrosis clinics, United Kingdom, 2009

P Seddon, K Fidler, S Raman, H Wyatt… - Emerging infectious …, 2013 - ncbi.nlm.nih.gov
Incidence of pulmonary infection with nontuberculous mycobacteria (NTM) is increasing
among persons with cystic fibrosis (CF). We assessed prevalence and management in CF …

[HTML][HTML] Nutritional status and pulmonary outcome in children and young people with cystic fibrosis

…, A Lunt, F Bartlett, F Perrin, CJ Bossley, HA Wyatt… - Respiratory …, 2018 - Elsevier
Background Nutrition is closely related to mortality and pulmonary and respiratory muscle
function in cystic fibrosis (CF) patients. We initially validated results from a bioelectrical …

Pulmonary function deficits in newborn screened infants with cystic fibrosis managed with standard UK care are mild and transient

…, SB Carr, C Wallis, H Wyatt… - European …, 2017 - Eur Respiratory Soc
With the advent of novel designer molecules for cystic fibrosis (CF) treatment, there is huge
need for early-life clinical trial outcomes, such as infant lung function (ILF). We investigated …

Multiplex genotyping for cystic fibrosis from filter paper blood spots

KH Poyser, HA Wyatt… - Annals of clinical …, 1998 - journals.sagepub.com
Cystic fibrosis is a common disease of the Caucasian population and is associated with
significant early mortality. We present a simple and rapid method for cystic fibrosis genotyping …

[HTML][HTML] A woman with cystic fibrosis, severe hypoxaemia, an atrial thrombus and a patent foramen ovale: a case report

NJ Simmonds, H Wyatt, R Patel, ME Hodson… - Journal of Medical Case …, 2009 - Springer
Introduction Cystic fibrosis is usually associated with chronic pulmonary sepsis and frequent
infective exacerbations. We report a very unusual cause of severe hypoxaemia in a woman …