Dr Keith Lindley
Credentials
• 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
News & Publications
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.
Refer your child to Dr Keith Lindley
Use the form below to refer your child for treatment. A member of our team will be in touch within 2 working days.
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