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For: Ricca I, Morani F, Bacci GM, Nesti C, Caputo R, Tessa A, Santorelli FM. Clinical and molecular studies in two new cases of ARSACS. Neurogenetics 2019;20:45-9. [PMID: 30680480 DOI: 10.1007/s10048-019-00564-7] [Cited by in Crossref: 14] [Cited by in F6Publishing: 14] [Article Influence: 4.7] [Reference Citation Analysis]
Number Citing Articles
1 Tremblay M, Girard-Côté L, Brais B, Gagnon C. Documenting manifestations and impacts of autosomal recessive spastic ataxia of Charlevoix-Saguenay to develop patient-reported outcome. Orphanet J Rare Dis 2022;17:369. [PMID: 36183078 DOI: 10.1186/s13023-022-02497-1] [Reference Citation Analysis]
2 Bagaria J, Bagyinszky E, An SSA. Genetics of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) and Role of Sacsin in Neurodegeneration. Int J Mol Sci 2022;23:552. [PMID: 35008978 DOI: 10.3390/ijms23010552] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
3 Riso V, Galatolo D, Barghigiani M, Galosi S, Tessa A, Ricca I, Rossi S, Caputi C, Cioffi E, Leuzzi V, Casali C, Santorelli FM, Silvestri G. A next generation sequencing-based analysis of a large cohort of ataxic patients refines the clinical spectrum associated with spinocerebellar ataxia 21. Eur J Neurol 2021;28:2784-8. [PMID: 33851480 DOI: 10.1111/ene.14868] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
4 Auburger G, Graeber MB, Ptáček LJ. Welcoming articles on genotype-dependent clinical features and diagnostics. Neurogenetics 2021;22:103-4. [PMID: 33792798 DOI: 10.1007/s10048-021-00638-5] [Reference Citation Analysis]
5 Wang Z, Song Y, Wang X, Li X, Xu F, Si L, Dong Y, Yao T, Zhu J, Lai H, Li W, Lin F, Huang H, Wang C. Autosomal recessive spastic ataxia of Charlevoix-Saguenay caused by novel mutations in SACS gene: A report of two Chinese families. Neurosci Lett 2021;752:135831. [PMID: 33746006 DOI: 10.1016/j.neulet.2021.135831] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
6 Longo F, De Ritis D, Miluzio A, Fraticelli D, Baets J, Scarlato M, Santorelli FM, Biffo S, Maltecca F. Sacsin cotranslational degradation causes autosomal recessive spastic ataxia of Charlevoix-Saguenay.. [DOI: 10.1101/2021.03.16.435646] [Reference Citation Analysis]
7 Morani F, Doccini S, Chiorino G, Fattori F, Galatolo D, Sciarrillo E, Gemignani F, Züchner S, Bertini ES, Santorelli FM. Functional Network Profiles in ARSACS Disclosed by Aptamer-Based Proteomic Technology. Front Neurol 2020;11:603774. [PMID: 33584503 DOI: 10.3389/fneur.2020.603774] [Cited by in Crossref: 4] [Cited by in F6Publishing: 7] [Article Influence: 4.0] [Reference Citation Analysis]
8 Martinelli C, Battaglini M, Pucci C, Gioi S, Caracci C, Macaluso G, Doccini S, Santorelli FM, Ciofani G. Development of Nanostructured Lipid Carriers for the Delivery of Idebenone in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay. ACS Omega 2020;5:12451-66. [PMID: 32548430 DOI: 10.1021/acsomega.0c01282] [Cited by in Crossref: 13] [Cited by in F6Publishing: 13] [Article Influence: 6.5] [Reference Citation Analysis]
9 Ricca I, Tessa A, Trovato R, Bacci GM, Santorelli FM. Docosahexaenoic acid in ARSACS: observations in two patients. BMC Neurol 2020;20:215. [PMID: 32466761 DOI: 10.1186/s12883-020-01803-3] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
10 Rudenskaya GE, Kadnikova VA, Ryzhkova OP. [Spastic ataxia of Charlevoix-Saguenay: the first Russian case report and literature review]. Zh Nevrol Psikhiatr Im S S Korsakova 2020;120:85-91. [PMID: 32307416 DOI: 10.17116/jnevro202012002185] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
11 Lieto M, Riso V, Galatolo D, De Michele G, Rossi S, Barghigiani M, Cocozza S, Pontillo G, Trovato R, Saccà F, Salvatore E, Tessa A, Filla A, Santorelli FM, De Michele G, Silvestri G. The complex phenotype of spinocerebellar ataxia type 48 in eight unrelated Italian families. Eur J Neurol 2020;27:498-505. [PMID: 31571321 DOI: 10.1111/ene.14094] [Cited by in Crossref: 28] [Cited by in F6Publishing: 33] [Article Influence: 9.3] [Reference Citation Analysis]
12 De Michele G, Lieto M, Galatolo D, Salvatore E, Cocozza S, Barghigiani M, Tessa A, Baldacci J, Pappatà S, Filla A, De Michele G, Santorelli FM. Spinocerebellar ataxia 48 presenting with ataxia associated with cognitive, psychiatric, and extrapyramidal features: A report of two Italian families. Parkinsonism Relat Disord 2019;65:91-6. [PMID: 31126790 DOI: 10.1016/j.parkreldis.2019.05.001] [Cited by in Crossref: 30] [Cited by in F6Publishing: 34] [Article Influence: 10.0] [Reference Citation Analysis]