Molecular pathology and genetics of congenital hepatorenal fibrocystic syndromes

Por Johnson, C, Gissen, P, Sergi, C
Publicado em 2003

Genetic and laboratory diagnostic approach in Niemann Pick disease type C

Por McKay Bounford, K., Gissen, P.
Publicado em 2014

Intentional overdose of warfarin in an adolescent: need for follow up

Por Ramanan, A, Gissen, P, Bose-Haider, B
Publicado em 2002

MR spectroscopy-based brain metabolite profiling in propionic acidaemia: metabolic changes in the basal ganglia during acute decompensation and effect of liver transplantation

Por Davison, James E, Davies, Nigel P, Wilson, Martin, Sun, Yu, Chakrapani, Anupam, McKiernan, Patrick J, Walter, John H, Gissen, P, Peet, Andrew C
Publicado em 2011

Use of next‐generation sequencing and candidate gene analysis to identify underlying defects in patients with inherited platelet function disorders

Por Leo, V. C., Morgan, N. V., Bem, D., Jones, M. L., Lowe, G. C., Lordkipanidzé, M., Drake, S., Simpson, M. A., Gissen, P., Mumford, A., Watson, S. P., Daly, M. E.
Publicado no J Thromb Haemost (2015)

A locus for asphyxiating thoracic dystrophy, ATD, maps to chromosome 15q13

Por Morgan, N, Bacchelli, C, Gissen, P, Morton, J, Ferrero, G, Silengo, M, Labrune, P, Casteels, I, Hall, C, Cox, P, Kelly, D, Trembath, R, Scambler, P, Maher, E, Goodman, F, Johnson, C
Publicado em 2003

Spectrum of movement disorders and neurotransmitter abnormalities in paediatric POLG disease

Por Papandreou, A., Rahman, S., Fratter, C., Ng, J., Meyer, E., Carr, L. J., Champion, M., Clarke, A., Gissen, P., Hemingway, C., Hussain, N., Jayawant, S., King, M. D., Lynch, B. J., Mewasingh, L., Patel, J., Prabhakar, P., Neergheen, V., Pope, S., Heales, S. J. R., Poulton, J., Kurian, Manju A.
Publicado no J Inherit Metab Dis (2018)

Correction to: Spectrum of movement disorders and neurotransmitter abnormalities in paediatric POLG disease

Por Papandreou, A., Rahman, S., Fratter, C., Ng, J., Meyer, E., Carr, L. J., Champion, M., Clarke, A., Gissen, P., Hemingway, C., Hussain, N., Jayawant, S., King, M. D., Lynch, B. J., Mewasingh, L., Patel, J., Prabhakar, P., Neergheen, V., Pope, S., Heales, S. J. R., Poulton, J., Kurian, Manju A.
Publicado no J Inherit Metab Dis (2018)