Moran, NF; Bain, MD; Muqit, MM; Bax, BE (2008) Carrier erythrocyte entrapped thymidine phosphorylase therapy for MNGIE. NEUROLOGY, 71 (9). 686 - 688 (6). ISSN 0028-3878 https://doi.org/10.1212/01.wnl.0000324602.97205.ab
SGUL Authors: Bax, Bridget Elizabeth

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Item Type:	Article
Additional Information:	PubMed ID: 18725595
Keywords:	Adult, Deoxyuridine, Drug Delivery Systems, Erythrocyte Transfusion, Erythrocytes, Fatal Outcome, Female, Gastrointestinal Diseases, Genetic Predisposition to Disease, Humans, Liver Diseases, Mitochondrial Diseases, Mutation, Peripheral Nervous System Diseases, Pneumonia, Syndrome, Thymidine, Thymidine Phosphorylase, Treatment Failure, Science & Technology, Life Sciences & Biomedicine, Clinical Neurology, Neurosciences & Neurology, MITOCHONDRIAL DISORDER, DEFICIENCY, THERAPY
SGUL Research Institute / Research Centre:	Academic Structure > Molecular and Clinical Sciences Research Institute (MCS) Academic Structure > Molecular and Clinical Sciences Research Institute (MCS) > Cell Sciences (INCCCS)
Journal or Publication Title:	NEUROLOGY
ISSN:	0028-3878
Related URLs:	Author
Dates:	Date Event 26 August 2008 Published
Web of Science ID:	WOS:000258725900013
URI:	https://openaccess.sgul.ac.uk/id/eprint/100448
Publisher's version:	https://doi.org/10.1212/01.wnl.0000324602.97205.ab

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