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70 Making clinical research a priority. The development of a research team within the adult cystic fibrosis service: A four year review of research activity and future prospects

Journal of cystic fibrosis, 2017-06, Vol.16, p.S82-S82

2017

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163 Acute pancreatitis in cystic fibrosis

Journal of cystic fibrosis, 2016-06, Vol.15, p.S92-S93

2016

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261 Audit and improvement of the cystic fibrosis liver service in a regional adult CF unit

Journal of cystic fibrosis, 2015-06, Vol.14, p.S125-S125

2015

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Impact of antibiotic treatment for pulmonary exacerbations on bacterial diversity in cystic fibrosis

Journal of cystic fibrosis, 2013-01, Vol.12 (1), p.22-28

2013

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How much of what you taught did your patients understand

Heart & lung, 2010, Vol.39 (4), p.371-372

2010

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DNMT3A and IDH mutations in acute myeloid leukemia and other myeloid malignancies: associations with prognosis and potential treatment strategies

Leukemia, 2014-09, Vol.28 (9), p.1774-1783

2014

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Effective targeting of primary human acute myeloid leukemia using anti-CD123 chimeric antigen receptor engineered T cells

Cytotherapy (Oxford, England), 2013-04, Vol.15 (4), p.S13-S14

2013

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WS8.4 Temporal bacterial community dynamics of cystic fibrosis lung infections

Journal of cystic fibrosis, 2013-06, Vol.12, p.S16-S16

2013

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Protein kinase C-mediated serine phosphorylation directly activates Raf-1 in murine hematopoietic cells

The Journal of biological chemistry, 1994-01, Vol.269 (2), p.1249-1256

1994

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Symptomatic sinus disease in cystic fibrosis and its effect on lung function

Journal of cystic fibrosis, 2010, Vol.9, p.S58-S58

2010

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104 Molecular analysis of diversity within the genus Pseudomonas in the lungs of cystic fibrosis patients

Journal of cystic fibrosis, 2007, Vol.6, p.S26-S26

2007

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Comparison of the lung bacterial communities sampled from stable cystic fibrosis patients over time

Journal of cystic fibrosis, 2008-06, Vol.7, p.S41-S41

2008

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Change in composition and structure of bacteria in the CF airway over one year

Journal of cystic fibrosis, 2009, Vol.8, p.S33-S33

2009

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80 Comparison of the bacterial communities sampled from the healthy and the cystic fibrosis lung

Journal of cystic fibrosis, 2007, Vol.6, p.S20-S20

2007

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Use of 16S rRNA Gene Profiling by Terminal Restriction Fragment Length Polymorphism Analysis To Compare Bacterial Communities in Sputum and Mouthwash Samples from Patients with Cystic Fibrosis

Journal of Clinical Microbiology, 2006-07, Vol.44 (7), p.2601-2604

2006

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The exclusion of dead bacterial cells is essential for accurate molecular analysis of clinical samples

Clinical microbiology and infection, 2010-11, Vol.16 (11), p.1656-1658

2010

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The impact of plasma 25-hydroxyvitamin d on lung function in patients with cystic fibrosis

Clinical nutrition ESPEN, 2020-12, Vol.40, p.537-538

2020

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DNMT3A and IDH mutations in acute myeloid leukemia and other myeloid malignancies: associations with prognosis and potential treatment strategies

Leukemia, 2015-02, Vol.29 (2), p.516-516

2015

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Characterization of high energy ion implantation into Ti–6Al–4V

Journal of nuclear materials, 2009-05, Vol.389 (2), p.248-253

2009

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Randomised controlled trial of nasal ventilation in acute ventilatory failure due to chronic obstructive airways disease

The Lancet (British edition), 1993-06, Vol.341 (8860), p.1555-1557

1993

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Catheter-related thrombosis associated with elevated factor VIII levels in cystic fibrosis

Journal of cystic fibrosis, 2006-08, Vol.5 (3), p.201-204

2006

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332: Alemtuzumab (ALEM) and Continuous-Infusion Pentostatin (PENTO): A Novel Nonmyeloablative (NM) Preparative Regimen for Allogeneic (allo) Hematopoietic Cell Transplantation (HCT)

Biology of blood and marrow transplantation, 2008, Vol.14 (2), p.122-122

2008

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250 Pancreatic enzyme use in adult patients with Cystic Fibrosis

Journal of cystic fibrosis, 2006, Vol.5, p.S58-S58

2006

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66 Bacterial diversity in the Cystic Fibrosis lung: geographical differences in community composition and distribution

Journal of cystic fibrosis, 2006, Vol.5, p.S15-S15

2006

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Erythropoietin induces Raf-1 activation and Raf-1 is required for erythropoietin-mediated proliferation

The Journal of biological chemistry, 1991-08, Vol.266 (23), p.14964-14969

1991

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70 Making clinical research a priority. The development of a research team within the adult cystic fibrosis service: A four year review of research activity and future prospects

163 Acute pancreatitis in cystic fibrosis

261 Audit and improvement of the cystic fibrosis liver service in a regional adult CF unit

Impact of antibiotic treatment for pulmonary exacerbations on bacterial diversity in cystic fibrosis

How much of what you taught did your patients understand

DNMT3A and IDH mutations in acute myeloid leukemia and other myeloid malignancies: associations with prognosis and potential treatment strategies

Effective targeting of primary human acute myeloid leukemia using anti-CD123 chimeric antigen receptor engineered T cells

WS8.4 Temporal bacterial community dynamics of cystic fibrosis lung infections

Protein kinase C-mediated serine phosphorylation directly activates Raf-1 in murine hematopoietic cells

Symptomatic sinus disease in cystic fibrosis and its effect on lung function

104 Molecular analysis of diversity within the genus Pseudomonas in the lungs of cystic fibrosis patients

Comparison of the lung bacterial communities sampled from stable cystic fibrosis patients over time

Change in composition and structure of bacteria in the CF airway over one year

80 Comparison of the bacterial communities sampled from the healthy and the cystic fibrosis lung

Use of 16S rRNA Gene Profiling by Terminal Restriction Fragment Length Polymorphism Analysis To Compare Bacterial Communities in Sputum and Mouthwash Samples from Patients with Cystic Fibrosis

The exclusion of dead bacterial cells is essential for accurate molecular analysis of clinical samples

The impact of plasma 25-hydroxyvitamin d on lung function in patients with cystic fibrosis

DNMT3A and IDH mutations in acute myeloid leukemia and other myeloid malignancies: associations with prognosis and potential treatment strategies

Characterization of high energy ion implantation into Ti–6Al–4V

Randomised controlled trial of nasal ventilation in acute ventilatory failure due to chronic obstructive airways disease

Catheter-related thrombosis associated with elevated factor VIII levels in cystic fibrosis

332: Alemtuzumab (ALEM) and Continuous-Infusion Pentostatin (PENTO): A Novel Nonmyeloablative (NM) Preparative Regimen for Allogeneic (allo) Hematopoietic Cell Transplantation (HCT)

250 Pancreatic enzyme use in adult patients with Cystic Fibrosis

66 Bacterial diversity in the Cystic Fibrosis lung: geographical differences in community composition and distribution

Erythropoietin induces Raf-1 activation and Raf-1 is required for erythropoietin-mediated proliferation

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