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Keith Lindley 医生

Consultant Paediatric Gastroenterologist
Dr Keith Lindley
Dr Keith Lindley

相关资质

• Inflammatory bowel disorders
• Motility disorders including Hirschsprungs and pseudoobstruction
• Neurogastroenterology
• Physiological evaluation of the GI tract
• Interventional endoscopy

Training:

• BSc (Hons) from London
• Postgraduate training in gastroenterology at GOSH
• PhD
• MB
• MRCP (UK)
• MRCPCH

Membership:

• Member of Royal College of Physicians
• Royal College of Paediatrics
• British Society of Gastroenterology
• Association of Physicians, Physiological Society
• Co-chair of the London Centre for Paediatric Neurogastroenterology and Motility
• Convenor of the Gastroenterology section of the Physiological Society

• Physiology of slow transit constipation
• Developing biomarkers of gastrointestinal food allergy
• Pathophysiology of food allergy induced gastroesophageal reflux
• Mucosal cytokine patterns in health and disease

新闻和论文发表

Tambucci, R., Thapar, N., Saliakellis, E., Pescarin, M., Quitadamo, P., Cristofori, F., Lindley, K.J., Borrelli, O., 2015. Clinical relevance of esophageal baseline impedance measurement: just an innocent bystander. J Pediatr Gastroenterol Nutr. 60(6) pp. 776-82.

Mutalib, M., Borrelli, O., Blackstock, S., Kiparissi, F., Elawad, M., Shah, N., Lindley, K., 2014. The use of sirolimus (rapamycin) in the management of refractory inflammatory bowel disease in children. J Crohns Colitis 8(12) pp. 1730-4.

Pacilli, M., Eaton, S., McHoney, M., Kiely, E.M., Drake, D.P., Curry, J.I., Lindley, K.J., Pierro, A., 2014. Four year follow-up of a randomised controlled trial comparing open and laparoscopic Nissen fundoplication in children. Arch Dis Child. 99(6) pp. 516-21.

Meyer, R., Fleming, C., Dominguez-Ortega, G., Lindley, K., Michaelis, L., Thapar, N., Elawad, M., Chakravarti, V., Fox, A.T., Shah, N., 2014. Manifestations of food protein induced gastrointestinal allergies presenting to a single tertiary paediatric gastroenterology unit. World Allergy Organ J. 6(1) p 13.

Shahni, R., Wedatilake, Y., Cleary, M.A., Lindley, K.J., Sibson, K.R., Rahman, S., 2013. A distinct mitochondrial myopathy, lactic acidosis and sideroblastic anemia (MLASA) phenotype associates with YARS2 mutations. Am J Med Genet A. 161A(9) pp. 2334-8.

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