Glycosphingolipid storage leads to the enhanced degradation of the B cell receptor in Sandhoff disease mice. by te Vruchte, D, Jeans, A, Platt, F, Sillence, D

Glycosphingolipid metabolism and its role in ageing and Parkinson’s disease by Wallom, K-L, Fernandez-Suarez, M, Priestman, D, Taylor-Te Vruchte, D, Platt, FM

Analysis of fluorescently labeled glycosphingolipid-derived oligosaccharides following ceramide glycanase digestion and anthranilic acid labeling. by Neville, D, Coquard, V, Priestman, D, te Vruchte, D, Sillence, D, Dwek, R, Platt, F, Butters, T

Plasma phosphorylated-tau217 is increased in Niemann–Pick disease type C by Gonzalez-Ortiz, F, Karikari, TK, Taylor-Te Vruchte, D, Shepherd, D, Kirsebom, B, Fladby, T, Platt, F, Blennow, K

Accumulation of glycosphingolipids in Niemann-Pick C disease disrupts endosomal transport. by te Vruchte, D, Lloyd-Evans, E, Veldman, R, Neville, D, Dwek, R, Platt, F, van Blitterswijk, W, Sillence, D

Treatment with miglustat reverses the lipid-trafficking defect in Niemann-Pick disease type C. by Lachmann, R, te Vruchte, D, Lloyd-Evans, E, Reinkensmeier, G, Sillence, D, Fernandez-Guillen, L, Dwek, R, Butters, T, Cox, T, Platt, F

NMR analysis reveals significant differences in the plasma metabolic profiles of Niemann Pick C1 patients, heterozygous carriers, and healthy controls. by Probert, F, Ruiz-Rodado, V, te Vruchte, D, Nicoli, E, Claridge, T, Wassif, C, Farhat, N, Porter, F, Platt, F, Grootveld, M

Glycosphingolipid changes in plasma in Parkinson’s disease independent of glucosylceramide levels by te Vruchte, D, Sturchio, A, Priestman, DA, Tsitsi, P, Hertz, E, Andréasson, M, Markaki, I, Wallom, K-L, Platt, F, Svenningsson, P

A sensitive and specific LC-MS/MS method for rapid diagnosis of Niemann-Pick C1 disease from human plasma. by Jiang, X, Sidhu, R, Porter, F, Yanjanin, N, Speak, A, te Vruchte, D, Platt, F, Fujiwara, H, Scherrer, D, Zhang, J, Dietzen, D, Schaffer, J, Ory, D

A novel approach to analyze lysosomal dysfunctions through subcellular proteomics and lipidomics: the case of NPC1 deficiency by Raghunath, A, Vermeire, W, Pauwels, J, Sannerud, R, Priestman, D, Te Vruchte, D, Vints, K, Baatsen, P, Decuypere, J, Lu, H, Martin, S, Vangheluwe, P, Swinnen, J, Lagae, L, Impens, F, Platt, F, Gevaert, K, Annaert, W

A novel approach to analyze lysosomal dysfunctions through subcellular proteomics and lipidomics: the case of NPC1 deficiency by Tharkeshwar, A, Trekker, J, Vermeire, W, Pauwels, J, Sannerud, R, Priestman, D, Te Vruchte, D, Vints, K, Baatsen, P, Decuypere, J, Li, H, Martin, S, Vangheluwe, P, Swinnen, J, Lagae, L, Impens, F, Platt, F, Gevaert, K, Annaert, W

Invariant natural killer T cells are not affected by lysosomal storage in patients with Niemann-Pick disease type C. by Speak, A, Platt, N, Salio, M, te Vruchte, D, Smith, D, Shepherd, D, Veerapen, N, Besra, G, Yanjanin, N, Simmons, L, Imrie, J, Wraith, J, Lachmann, R, Hartung, R, Runz, H, Mengel, E, Beck, M, Hendriksz, C, Porter, F, Cerundolo, V, Platt, F