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Diagnosis and management of progressive ataxia in adults.
de Silva RN, Vallortigara J, Greenfield J, Hunt B, Giunti P, Hadjivassiliou M. de Silva RN, et al. Among authors: greenfield j. Pract Neurol. 2019 Jun;19(3):196-207. doi: 10.1136/practneurol-2018-002096. Epub 2019 May 2. Pract Neurol. 2019. PMID: 31048364 Free PMC article. Review.
Guidelines on the diagnosis and management of the progressive ataxias.
de Silva R, Greenfield J, Cook A, Bonney H, Vallortigara J, Hunt B, Giunti P. de Silva R, et al. Among authors: greenfield j. Orphanet J Rare Dis. 2019 Feb 20;14(1):51. doi: 10.1186/s13023-019-1013-9. Orphanet J Rare Dis. 2019. PMID: 30786918 Free PMC article. Review.
Correction to: DRPLA: understanding the natural history and developing biomarkers to accelerate therapeutic trials in a globally rare repeat expansion disorder.
Chaudhry A, Athanasiou-Fragkouli A, Garcia-Moreno H, Abadias SP, Greenfield J, Shiloh-Malawsky Y, Giunti P, Houlden H. Chaudhry A, et al. Among authors: greenfield j. J Neurol. 2021 Aug;268(8):3042. doi: 10.1007/s00415-021-10644-0. J Neurol. 2021. PMID: 34152486 Free PMC article. No abstract available.
The attitude of patients with progressive ataxias towards clinical trials.
Thomas-Black G, Dumitrascu A, Garcia-Moreno H, Vallortigara J, Greenfield J, Hunt B, Walther S, Wells M, Lynch DR, Montgomery H, Giunti P. Thomas-Black G, et al. Among authors: greenfield j. Orphanet J Rare Dis. 2022 Jan 4;17(1):1. doi: 10.1186/s13023-021-02091-x. Orphanet J Rare Dis. 2022. PMID: 34983593 Free PMC article.
Patient pathways for rare diseases in Europe: ataxia as an example.
Vallortigara J, Greenfield J, Hunt B, Hoffman D, Reinhard C, Graessner H, Federico A, Quoidbach V, Morris S, Giunti P. Vallortigara J, et al. Among authors: greenfield j. Orphanet J Rare Dis. 2023 Oct 17;18(1):328. doi: 10.1186/s13023-023-02907-y. Orphanet J Rare Dis. 2023. PMID: 37848998 Free PMC article.
819 results