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For: Meyyazhagan A, Orlacchio A. Hereditary Spastic Paraplegia: An Update. Int J Mol Sci 2022;23:1697. [PMID: 35163618 DOI: 10.3390/ijms23031697] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 8.0] [Reference Citation Analysis]
Number Citing Articles
1 Nunes LGA, Pitts MW, Hoffmann PR. Selenoprotein I (selenoi) as a critical enzyme in the central nervous system. Arch Biochem Biophys 2022;:109376. [PMID: 36007576 DOI: 10.1016/j.abb.2022.109376] [Reference Citation Analysis]
2 Meyyazhagan A, Kuchi Bhotla H, Pappuswamy M, Orlacchio A. The Puzzle of Hereditary Spastic Paraplegia: From Epidemiology to Treatment. IJMS 2022;23:7665. [DOI: 10.3390/ijms23147665] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Tian W, Zheng H, Zhu Z, Zhang C, Luan X, Cao L. New phenotype of RTN2-related spectrum: Complicated form of spastic paraplegia-12. Ann Clin Transl Neurol 2022. [PMID: 35684947 DOI: 10.1002/acn3.51605] [Reference Citation Analysis]
4 Shi Y, Wang A, Chen B, Wang X, Niu S, Li W, Li S, Zhang Z. Clinical Features and Genetic Spectrum of Patients With Clinically Suspected Hereditary Progressive Spastic Paraplegia. Front Neurol 2022;13:872927. [PMID: 35572931 DOI: 10.3389/fneur.2022.872927] [Reference Citation Analysis]