P. Weller

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Creon 10,000 Minimicrospheres vs. Creon 8,000 microspheres--an open randomised crossover preference study.

A. Macdonald, C. Patchell, M. Desai, 2002, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Two enteric coated microspheres in cystic fibrosis.

J. Williams, A. Macdonald, P. Weller, 1990, Archives of disease in childhood.

Outer membrane antigens of mucoid Pseudomonas aeruginosa isolated directly from the sputum of a cystic fibrosis patient

Michael R. W. Brown, P. Weller, H. Anwar, 1984 .

Clinical benefit from nebulized human recombinant DNase in Kartagener's syndrome

M. Desai, P. Weller, M. Desai, 1995, Pediatric pulmonology.

Subspecific differentiation of Burkholderia cepacia isolates in cystic fibrosis.

D. Allison, N. Høiby, P. Lambert, 1998, Journal of medical microbiology.

Transplantation for cystic fibrosis: Outcome following early liver transplantation

J. Buckels, R. Bonser, D. Mirza, 2002, Journal of gastroenterology and hepatology.

Comparison of fluticasone propionate and sodium cromoglycate for the treatment of childhood asthma (an open parallel group study).

J. Price, P. Weller, J. Price, 1995, Respiratory medicine.

Asthma treatment and growth

N. Shaw, P. Weller, N. Fraser, 1997, Archives of disease in childhood.

Management of Asthma

P. Weller, 1990, Archives of disease in childhood.

Increase in incidence of childhood empyema in West Midlands, UK

P. Weller, D. Spencer, D. Parikh, 1997, The Lancet.

Lipopolysaccharide antigens produced by Pseudomonas aeruginosa from cystic fibrosis lung infection

Michael R. W. Brown, P. Weller, D. M. Cochrane, 1988 .

Pitfalls in the diagnosis of appendix abscess in cystic fibrosis.

P. Weller, H. L. Smith, S. Chapman, 1989, Journal of the Royal Society of Medicine.

Hypercholesterolaemia and hypertriglyceridaemia in patients with analgesic nephropathy.

G. Wambach, P. Weller, A. Helber, 1980, Nephron.

Urinary incontinence in 9-16 year olds with cystic fibrosis compared to other respiratory conditions and a normal group.

M. Desai, P. Weller, W. Browne, 2009, Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society.

Cough plate versus cough swab in patients with cystic fibrosis; a pilot study

M. Desai, P. Weller, J. Gray, 2004, Archives of Disease in Childhood.

The sweat test.

P. Weller, P. Griffiths, A. Green, 1987, Archives of disease in childhood.

Serum IgG response to an outer membrane porin protein of Burkholderia cepacia in patients with cystic fibrosis.

P. Lambert, A. W. Smith, M. R. Brown, 1997, FEMS immunology and medical microbiology.

Serum IgG response to Burkholderia cepacia outer membrane antigens in cystic fibrosis: assessment of cross-reactivity with Pseudomonas aeruginosa.

G. Smith, A. W. Smith, M. R. Brown, 1995, FEMS immunology and medical microbiology.

PHARYNGEAL LECITHIN/SPHINGOMYELIN RATIOS IN NEWBORN INFANTS

J. Baum, P. Jenkins, P. Weller, 1976, The Lancet.

Successful treatment of invasive pulmonary aspergillosis in chronic granulomatous disease with orally administered itraconazole suspension.

P. Weller, D. Spencer, P. Darbyshire, 1994, American journal of respiratory and critical care medicine.

PUVA therapy for drug-resistant graft-versus-host disease.

K. Atkinson, J. Biggs, P. Weller, 1986, Bone marrow transplantation.

Salmeterol xinafoate in children on high dose inhaled steroids.

G. Russell, D. Williams, J. Price, 1995, Annals of allergy, asthma & immunology : official publication of the American College of Allergy, Asthma, & Immunology.

Antibody response to Pseudomonas aeruginosa surface protein antigens in a rat model of chronic lung infection.

J. Costerton, M. R. Brown, P. Weller, 1988, Journal of medical microbiology.

Silastic catheters for antibiotics in cystic fibrosis.

J. Williams, P. Weller, C. Woods, 1988, Archives of disease in childhood.

Chronic granulomatous disease presenting in childhood with Pseudomonas cepacia septicaemia.

A. Goldstein, P. Weller, D. Spencer, 1993, The Journal of infection.

Tracheal compression caused by Achalasia

P. Weller, S. Chapman, R. Buick, 1989, Pediatric pulmonology.

Increasing resistance of planktonic and biofilm cultures of Burkholderia cepacia to ciprofloxacin and ceftazidime during exponential growth.

M. R. Brown, T. Bühler, M. Desai, 1998, The Journal of antimicrobial chemotherapy.

Cystic fibrosis in children from ethnic minorities in the West Midlands.

S. Higgins, P. Weller, D. Spencer, 1994, Respiratory medicine.

Comparison of two percutaneous intravenous "midline" catheters in cystic fibrosis.

G. Ruiz, P. Weller, D. Spencer, 1996, Journal of intravenous nursing : the official publication of the Intravenous Nurses Society.

Free cortisol and creatinine in urine of healthy children.

B. Rudd, P. Weller, A. Day, 1987, Clinical chemistry.

Multicenter, open‐label study of recombinant human DNase in cystic fibrosis patients with moderate lung disease

B. Strandvik, R. Kraemer, E. Matouk, 1998, Pediatric pulmonology.

Combined percutaneous lung biopsy and high‐resolution computed tomography in the diagnosis and management of lung disease in children

F. Raafat, H. Alton, P. Weller, 1996, Pediatric pulmonology.

Recommendations for the use of palivizumab as prophylaxis against respiratory syncytial virus in infants with congenital cardiac disease

F. Casey, W. Lenney, M. Blackburn, 2003, Cardiology in the Young.

Neonatal screening--should we or shouldn't we?

P. Weller, J. V. West, 1991, Journal of the Royal Society of Medicine.

Spontaneous rupture of the diaphragm

A. Akbar, H. Alton, P. Weller, 1999, Archives of disease in childhood.

Sweat sodium is not sweat chloride

A. Green, P. Weller, S. Hall, 1997, Archives of disease in childhood.

Delayed diagnosis of cystic fibrosis in children from ethnic minorities

P. Weller, D. Spencer, M. Venkataraman, 1993, The Lancet.

Clinical features, pathogenesis and management of meconium ileus equivalent.

P. Weller, J. Williams, 1986, Journal of the Royal Society of Medicine.

Sweat tests and flucloxacillin.

J. Williams, P. Weller, P. Griffiths, 1988, Archives of disease in childhood.

A high incidence of asthma and respiratory symptoms in 4-11 year old children.

A. Sykes, J. Ayres, P. Weller, 1992, Respiratory medicine.

Dornase-alfa for cystic fibrosis

P. Weller, D. Spencer, 1995, The Lancet.

Implications of early inflammation and infection in cystic fibrosis: A review of new and potential interventions

P. Weller, 1997, Pediatric pulmonology.