C. Wallis

发表

The evolution of airway function in early childhood following clinical diagnosis of cystic fibrosis.

A. Wade, J. Stocks, A. Hoo, 2004, American journal of respiratory and critical care medicine.

Recombinant human deoxyribonuclease for cystic fibrosis.

C. Wallis, A. Jones, Ashley P. Jones, 2003, The Cochrane database of systematic reviews.

Clinical outcomes of congenital lung abnormalities.

C. Wallis, 2000, Paediatric respiratory reviews.

Central microtubular agenesis causing primary ciliary dyskinesia.

C. O’Callaghan, C. Wallis, W. Stannard, 2004, American journal of respiratory and critical care medicine.

Filamin A (FLNA) mutation—A newcomer to the childhood interstitial lung disease (ChILD) classification

M. Ashworth, S. Shelmerdine, C. Owens, 2017, Pediatric pulmonology.

Unsupervised phenotypic clustering for determining clinical status in children with cystic fibrosis

S. Stanojevic, N. Sebire, F. Ratjen, 2021, European Respiratory Journal.

Slide tracheoplasty

M. Elliott, C. Wallis, B. Hartley, 2008, Current opinion in otolaryngology & head and neck surgery.

Nontuberculous mycobacterial disease in adult cystic fibrosis patients.

B. Ramsey, C. Nolan, C. Wallis, 1993, Chest.

Tracheomalacia and bronchomalacia in children: response to the ERS statement

A. Chang, F. Midulla, J. Bhatt, 2019, European Respiratory Journal.

Diagnosis and Presentation of Cystic Fibrosis

C. Wallis, 2019, Kendig's Disorders of the Respiratory Tract in Children.

Chapter 60 – Diagnosis and Presentation of Cystic Fibrosis

C. Wallis, 2006 .

The 100,000 Genomes Pilot on Rare Disease Diagnosis in Healthcare − A Preliminary Report

Julius O. B. Jacobsen, Robert W. Taylor, Eleanor F. Dewhurst, 2021, The New England journal of medicine.

The role of the pediatrician in caring for children with tracheobronchomalacia

A. Chang, A. Bush, J. Bhatt, 2020, Expert review of respiratory medicine.

Effects of recombinant human DNase and hypertonic saline on airway inflammation in children with cystic fibrosis.

C. Metcalfe, A. Bush, J. Shute, 2002, American journal of respiratory and critical care medicine.

Bronchoconstriction following nebulised colistin in cystic fibrosis

S. Cunningham, S. Carr, C. Wallis, 2001, Archives of disease in childhood.

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

A. Wade, J. Stocks, A. Hoo, 2002, American journal of respiratory and critical care medicine.

V. Ricotti, F. Muntoni, L. Servais, 2021, Muscle & nerve.

Growth, Body Composition, and Lung Function in Prepubertal Children with Cystic Fibrosis Diagnosed by Newborn Screening.

R. Grant, M. Fewtrell, C. Wallis, 2020, Nutrition in clinical practice : official publication of the American Society for Parenteral and Enteral Nutrition.

Cardiorespiratory Progression Over 5 Years and Role of Corticosteroids in Duchenne Muscular Dystrophy

C. G. Tay, F. Muntoni, P. Munot, 2020, Chest.

Cardiorespiratory progression over 5 years and role of corticosteroids in DMD: a single site retrospective longitudinal study.

C. G. Tay, F. Muntoni, M. Burch, 2020, Chest.

Safety and use of sputum induction in children with cystic fibrosis

C. Metcalfe, A. Bush, J. Shute, 2003, Pediatric pulmonology.

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

A. Wade, J. Stocks, G. Hülskamp, 2007, Thorax.

Who needs chest physiotherapy? Moving from anecdote to evidence

C. Wallis, Ammani Prasad, 1999, Archives of disease in childhood.

Assessing the Role of Aspiration in Pediatric Lung Disease

C. Wallis, M. Ryan, 2012 .

Cerebro–costo–mandibular syndrome: Clinical, radiological, and genetic findings

E. Zackai, J. Clayton-Smith, R. Scott, 2016, American journal of medical genetics. Part A.

Predicting response to rhDNase and hypertonic saline in children with cystic fibrosis

C. Metcalfe, A. Bush, C. Wallis, 2004, Pediatric pulmonology.

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

A. Wade, J. Stocks, A. Hoo, 2017, European Respiratory Journal.

Mucolytic Therapy in Cystic Fibrosis

C. Wallis, 2001, Journal of the Royal Society of Medicine.

Transition of care in children with chronic disease

C. Wallis, 2007, BMJ : British Medical Journal.

The influence of stents on microbial colonization of the airway in children after slide tracheoplasty: A 14‐year single‐center experience

M. Elliott, C. Butler, R. Hewitt, 2015, Pediatric pulmonology.

An evaluation of two aerosol delivery systems for rhDNase.

D. Geddes, P. Shah, M. Hodson, 1997, The European respiratory journal.

Dornase alfa for cystic fibrosis.

C. Wallis, A. Jones, 2010, The Cochrane database of systematic reviews.

Lung function from infancy to the preschool years after clinical diagnosis of cystic fibrosis.

S. Stanojevic, A. Wade, J. Stocks, 2008, American journal of respiratory and critical care medicine.

Atypical cystic fibrosis: diagnostic and management dilemmas

C. Wallis, 2003 .

Is chest CT useful in newborn screened infants with cystic fibrosis at 1 year of age?

A. Wade, J. Stocks, A. McEwan, 2013, Thorax.

M. Irving, C. Wallis, V. Gowda, 2021, Clinical dysmorphology.

ERS statement on tracheomalacia and bronchomalacia in children

I. Masters, A. Chang, E. Alexopoulou, 2019, European Respiratory Journal.

Tracheobronchial stenting for airway malacia.

C. Wallis, C. McLaren, 2017, Paediatric respiratory reviews.

Paediatric interstitial lung disease (PILD)—An update

R. Dinwiddie, C. Wallis, 2006 .

Ten‐year follow up of hydroxychloroquine treatment for ABCA3 deficiency

C. Wallis, M. Williamson, 2014, Pediatric pulmonology.

Mutations of CFTR gene and intermediate sweat chloride levels.

A. Bush, C. Wallis, 2003, American journal of respiratory and critical care medicine.

Diagnosing cystic fibrosis: blood, sweat, and tears

C. Wallis, 1997, Archives of disease in childhood.

Stool elastase as a diagnostic test for pancreatic function in children with cystic fibrosis

T. Leung, D. Cubitt, C. Wallis, 1997, The Lancet.

Archives of Disease in Childhood focuses on all aspects of child health and disease from the perinatal period through adolescence

T. Cole, B. Phillips, S. Behjati, 2015 .

International Consensus Statement on the diagnosis, multidisciplinary management and lifelong care of individuals with achondroplasia

G. Mortier, J. Campbell, M. Sessa, 2021, Nature Reviews Endocrinology.

Fetal Lung Lesions

P. Pandya, C. Wallis, A. Yulia, 2020 .

Pulmonary alveolar microlithiasis in childhood: Diagnosis by transbronchial biopsy

R. Dinwiddie, C. Wallis, M. Malone, 1996, Pediatric pulmonology.

Primary thoracoscopic treatment of empyema in children.

M. Elliott, V. Hjortdal, R. Dinwiddie, 2003, The Journal of thoracic and cardiovascular surgery.

Pulmonary hemorrhage in type 3 Gaucher disease: a case report

M. Ashworth, A. Vellodi, C. Wallis, 2010, Journal of Inherited Metabolic Disease.

Mutations in radial spoke head protein genes RSPH9 and RSPH4A cause primary ciliary dyskinesia with central-microtubular-pair abnormalities.

Colin A. Johnson, R. J. Herrera, Stephen W. Wilson, 2009, American journal of human genetics.

Diagnosis of cystic fibrosis in London and South East England before and after the introduction of newborn screening

P. Seddon, J. Price, R. Chavasse, 2013, Archives of Disease in Childhood.

Minimal change in structural, functional and inflammatory markers of lung disease in newborn screened infants with cystic fibrosis at one year.

A. Wade, J. Stocks, A. Hoo, 2020, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Cystic fibrosis newborn screening: outcome of infants with normal sweat tests

C. Nwokoro, G. Ruiz, C. Edmondson, 2017, Archives of Disease in Childhood.

Cystic fibrosis and Russell‐Silver syndrome in a child with maternal isodisomy of chromosome 7

K. Prescott, R. Dinwiddie, C. Wallis, 2005, Pediatric pulmonology.

Long-segment tracheal stenosis: slide tracheoplasty and a multidisciplinary approach improve outcomes and reduce costs.

M. Elliott, Q. Mok, C. Wallis, 2004, The Journal of thoracic and cardiovascular surgery.

The management of congenital tracheal stenosis.

Colin Wallis, Catherine Dunne, Quen Mok, 2003, International journal of pediatric otorhinolaryngology.

The Clinical Outcome of Antenatally Diagnosed Cystic Lung Lesions

C. Wallis, 2001 .

The natural history of prenatally diagnosed congenital cystic lung lesions: long-term follow-up of 119 cases

M. Ashworth, P. de Coppi, L. Chitty, 2017, Archives of Disease in Childhood.

An infant with a persistent cough and an unusual course of the nasogastric tube

C. Wallis, P. Aurora, E. Leith, 2018, Archives of Disease in Childhood.

Pulmonary mass in an infant

N. Sebire, D. Lumsden, C. Wallis, 2009, European Respiratory Journal.

Severe bronchomalacia treated by combination of Nuss procedure and aortopexy: an unusual therapy combination.

M. Elliott, C. Wallis, D. Roebuck, 2011, The Annals of thoracic surgery.

The successful use of the nasopharyngeal airway in Pierre Robin sequence: an 11-year experience

C. Wallis, M. Wyatt, F. Abel, 2012, Archives of Disease in Childhood.

Tracheal Replacement Therapy with a Stem Cell‐Seeded Graft: Lessons from Compassionate Use Application of a GMP‐Compliant Tissue‐Engineered Medicine

M. Elliott, P. de Coppi, R. Hewitt, 2017, Stem cells translational medicine.

Multiple-breath washout as a marker of lung disease in preschool children with cystic fibrosis.

Janet Stocks, Colin Wallis, Paul Aurora, 2005, American journal of respiratory and critical care medicine.

The feasibility of home monitoring of young people with cystic fibrosis: Results from CLIMB-CF.

J. Wallenburg, S. Macfarlane, J. Davies, 2021, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

A comparative study of hypertonic saline, daily and alternate-day rhDNase in children with cystic fibrosis.

C. Metcalfe, A. Bush, R. Grieve, 2002, Health technology assessment.

Bronchial provocation testing with dry powder mannitol in children with cystic fibrosis

Colin Wallis, Chris Metcalfe, Andrew Bush, 2008, Pediatric pulmonology.

Assessing the usefulness of outcomes measured in a cystic fibrosis treatment trial.

C. Metcalfe, A. Bush, C. Wallis, 2007, Respiratory medicine.

Comparison of hypertonic saline and alternate-day or daily recombinant human deoxyribonuclease in children with cystic fibrosis: a randomised trial

R. Grieve, M. Flather, S. Thompson, 2001, The Lancet.

The role of the nasopharyngeal prong in craniofacial disorders in particular the Pierre Robin sequence.

C. Wallis, F. Abel, 2021, Seminars in fetal & neonatal medicine.

Extra corporeal membrane oxygenation (ECMO) therapy in a 3-year-old child with cystic fibrosis: A tale of hope

C. Wallis, P. Stafler, 2009, Journal of the Royal Society of Medicine.

Management: Non-invasive home ventilation

C. Wallis, 2000 .

Managing infants with craniofacial malformations - Where to go next?

C. Poets, V. Abadie, C. Wiechers, 2021, Seminars in fetal & neonatal medicine.

Effects of hypertonic saline, alternate day and daily rhDNase on healthcare use, costs and outcomes in children with cystic fibrosis

C. Metcalfe, A. Bush, R. Grieve, 2002, Thorax.

Teamwork in Airway Surgery

M. Elliott, R. Hewitt, C. Wallis, 2021, Frontiers in Pediatrics.

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

A. Wade, J. Stocks, K. Costeloe, 2012, Thorax.

Deaths in childhood from cystic fibrosis: 10-year analysis from two London specialist centres

Colin Wallis, C. Wallis, I. Balfour-Lynn, 2012, Archives of Disease in Childhood.

Investigation and management of the long-term ventilated premature infant.

C. Wallis, M. Wright, 2018, Early human development.

Comparison of inhaled mannitol, daily rhDNase and a combination of both in children with cystic fibrosis: a randomised trial

C. Metcalfe, A. Bush, C. Wallis, 2009, Thorax.

Dornase alfa for cystic fibrosis

M. Rosenthal, D. Geddes, M. Hodson, 1995, BMJ.

Multiple breath inert gas washout as a measure of ventilation distribution in children with cystic fibrosis

J. Stocks, A. Bush, P. Gustafsson, 2004, Thorax.

Time to think again: Cystic fibrosis is not an “all or none” disease

C. Wallis, A. Bush, 2000, Pediatric pulmonology.

Unsupervised home spirometry is not equivalent to supervised clinic spirometry in children and young people with cystic fibrosis: Results from the CLIMB‐CF study

M. Rosenthal, J. Wallenburg, E. Alton, 2023, Pediatric pulmonology.

Primary pulmonary lymphangiectasis in a premature infant: Resolution following intensive care

C. Owens, R. Dinwiddie, C. Wallis, 2003, Pediatric pulmonology.

Retrospective review of the effects of rhDNase in children with cystic fibrosis

M. Rosenthal, A. Bush, J. Davies, 1997, Pediatric pulmonology.

Lung function from infancy to the preschool years after clinical diagnosis of cystic fibrosis.

S. Stanojevic, A. Wade, J. Stocks, 2008, American journal of respiratory and critical care medicine.

Multiple breath inert gas washout as a measure of ventilation distribution in children with cystic fibrosis

J. Stocks, A. Bush, A. Lindblad, 2004, Thorax.

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

A. Wade, J. Stocks, G. Hülskamp, 2007, Thorax.

Dornase alfa for cystic fibrosis. Patients should not be denied a safe, effective treatment.

M. Rosenthal, D. Geddes, M. Hodson, 1995, BMJ.

Mutations in radial spoke head protein genes RSPH9 and RSPH4A cause primary ciliary dyskinesia with central-microtubular-pair abnormalities.

Colin A. Johnson, R. J. Herrera, Stephen W. Wilson, 2009, American journal of human genetics.

The Chrispin–Norman score in cystic fibrosis: doing away with the lateral view

C. Benden, C. Owens, R. Dinwiddie, 2005, European Respiratory Journal.

EARLY DETECTION OF LUNG DISEASE IN INFANTS WITH CYSTIC FIBROSIS DIAGNOSED BY NEWBORN SCREENING (NBS)

J. Stocks, A. Hoo, S. Lum, 2010 .

Dornase alfa for cystic fibrosis.

C. Wallis, A. Jones, 2010, The Cochrane database of systematic reviews.