المؤلفون: Fields, T.^Aff1, Patterson, M., Bremova-Ertl, T., Belcher, G., Billington, I., Churchill, G. C., Davis, W., Evans, W.^{Aff7, Aff8}, Flint, S., Galione, A., Granzer, U., Greenfield, J., Karl, R., Kay, R., Lewi, D., Mathieson, T., Meyer, T., Pangonis, D., Platt, F. M., Tsang, L., Verburg, C., Factor, M., Strupp, M.^Aff17

المصدر: Trials. 22(1)

المؤلفون: Höglinger, D.^{Aff1, Aff2}, Burgoyne, T.^{Aff3, Aff4}, Sanchez-Heras, E., Hartwig, P., Colaco, A.^{Aff1, Aff5}, Newton, J., Futter, C. E., Spiegel, S., Platt, F. M., Eden, E. R^Aff3

المصدر: Nature Communications. 10(1)

المؤلفون: Butters, T. D.^Aff2, Dwek, R. A.^Aff2, Platt, F. M.^Aff2

المساهمون: Axford, John S., editor^Aff1

المصدر: Glycobiology and Medicine. 535:219-226

المؤلفون: D’Amore, Simona, Page, Kathleen, Donald, Aimée, Taiyari, Khadijeh, Tom, Brian, Deegan, Patrick, Tan, Chong Y., Poole, Kenneth, Jones, Simon A., Mehta, Atul, Hughes, Derralynn, Sharma, Reena, Lachmann, Robin H., Chakrapani, Anupam, Geberhiwot, Tarekegn, Santra, Saikat, Banka, Siddarth, Cox, Timothy M., Cox, T. M., Platt, F. M., Banka, S., Chakrapani, A., Deegan, P. B., Geberhiwot, T., Hughes, D. A., Jones, S., Lachmann, R. H., Santra, S., Sharma, R., Vellodi, A.

المساهمون: Cox, Timothy M [0000-0002-4951-9941], Apollo - University of Cambridge Repository, Cox, Timothy M. [0000-0002-4951-9941]

المصدر: Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-22 (2021)
Orphanet Journal of Rare Diseases

مصطلحات موضوعية: Pediatrics, medicine.medical_specialty, medicine.medical_treatment, Splenectomy, Disease, Cohort Studies, Lysosomal storage diseases, medicine, Humans, Disease-modifying therapies, GAUCHERITE, Pharmacology (medical), Substrate reduction therapy, Prospective Studies, Bone pain, Genetics (clinical), Retrospective Studies, Gaucher Disease, business.industry, Research, Cohort, Genetic disorder, General Medicine, Enzyme replacement therapy, medicine.disease, Orthopedic surgery, Medicine, Glucosylceramidase, Nervous System Diseases, medicine.symptom, business

وصف الملف: application/pdf; application/zip; text/xml

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2019fd6ca96eb1cda8c25a96cb5b49d
https://doi.org/10.1186/s13023-021-02034-6

المؤلفون: Hurst, C D, Tomlinson, D C, Williams, S V, Platt, F M, Knowles, M A^{Aff1, ID1210934_cor5}

المصدر: Oncogene. 27(19):2716-2727

المؤلفون: Heare, T., Alp, N. J., Priestman, D. A., Kulkarni, A. B., Qasba, P., Butters, T. D., Dwek, R. A., Clarke, K., Channon, K. M., Platt, F. M.

المصدر: Journal of Inherited Metabolic Disease: Official Journal of the Society for the Study of Inborn Errors of Metabolism. February 2007 30(1):79-87

المؤلفون: Elstein, D., Hollak, C., Aerts, J. M. F. G., van Weely, S., Maas, M., Cox, T. M., Lachmann, R. H., Hrebicek, M., Platt, F. M., Butters, T. D., Dwek, R. A., Zimran, A.

المصدر: Journal of Inherited Metabolic Disease: Official Journal of the Society for the Study of Inborn Errors of Metabolism. November 2004 27(6):757-766

المؤلفون: Platt, F. M., Jeyakumar, M., Andersson, U., Priestman, D. A., Dwek, R. A., Butters, T. D., Cox, T. M., Lachmann, R. H., Hollak, C., Aerts, J. M. F. G., Van Weely, S., Hrebícek, M., Moyses, C., Gow, I., Elstein, D., Zimran, A.

المصدر: Journal of Inherited Metabolic Disease: Official Journal of the Society for the Study of Inborn Errors of Metabolism. April 2001 24(2):275-290

المؤلفون: Gascon, J. M., Oliveri, V., Mcgown, A., Kaya, E., Chen, Y. -L., Austin, C., Walker, M., Platt, F. M., Vecchio, G., Spencer, J.

المصدر: Chemmedchem

مصطلحات موضوعية: Cyclodextrins, antioxidant, Full Paper, deferasirox, iron complexes, Niemann–Pick, protein aggregation, CHO Cells, Hep G2 Cells, Full Papers, Iron Chelating Agents, Antioxidants, Deferasirox, Cricetulus, alpha-Synuclein, Animals, Humans, Protein Multimerization

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::9ef836be8dfab74e6c012f0b66ea7e77
https://pubmed.ncbi.nlm.nih.gov/31162826

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