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Cited by in F6Publishing
For: Ebrahimi-Fakhari D, Alecu JE, Ziegler M, Geisel G, Jordan C, D'Amore A, Yeh RC, Akula SK, Saffari A, Prabhu SP, Sahin M, Yang E; International AP-4-HSP Registry and Natural History Study. Systematic Analysis of Brain MRI Findings in Adaptor Protein Complex 4-Associated Hereditary Spastic Paraplegia. Neurology 2021;97:e1942-54. [PMID: 34544818 DOI: 10.1212/WNL.0000000000012836] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Kunta AR, Jueng J, Jordan C, Kojic J, Mo A, Ebrahimi-fakhari D. Blended Phenotype of Prader-Willi Syndrome and HSP-SPG11Caused by Maternal Uniparental Isodisomy. Neurol Genet 2022;8:e200041. [DOI: 10.1212/nxg.0000000000200041] [Reference Citation Analysis]
2 Innes EA, Goetti R, Mahant N, Ho G, Williams L, Gill D, Dale RC, Mohammad SS. SPG11 presenting with dystonic tremor in childhood. Parkinsonism Relat Disord 2022;99:76-8. [PMID: 35617747 DOI: 10.1016/j.parkreldis.2022.05.011] [Reference Citation Analysis]