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For: Lallemant-Dudek P, Darios F, Durr A. Recent advances in understanding hereditary spastic paraplegias and emerging therapies. Fac Rev 2021;10:27. [PMID: 33817696 DOI: 10.12703/r/10-27] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
Number Citing Articles
1 Komachali SR, Siahpoosh Z, Salehi M. Two novel mutations in ALDH18A1 and SPG11 gene found by whole-exome sequencing in spastic paraplegia disease patients in Iran. Genomics Inform 2022;20:e30. [DOI: 10.5808/gi.22030] [Reference Citation Analysis]
2 Strijkova V, Todinova S, Andreeva T, Langari A, Bogdanova D, Zlatareva E, Kalaydzhiev N, Milanov I, Taneva SG. Platelets’ Nanomechanics and Morphology in Neurodegenerative Pathologies. Biomedicines 2022;10:2239. [DOI: 10.3390/biomedicines10092239] [Reference Citation Analysis]
3 Laßmann C, Ilg W, Schneider M, Völker M, Haeufle DFB, Schüle R, Giese M, Synofzik M, Schöls L, Rattay TW. Specific Gait Changes in Prodromal Hereditary Spastic Paraplegia Type 4: preSPG4 Study. Mov Disord 2022. [PMID: 36054444 DOI: 10.1002/mds.29199] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
4 MacWilliams BA, Carroll KL, Stotts AK, Kerr LM, Schwartz MH. Discrimination between hereditary spastic paraplegia and cerebral palsy based on gait analysis data: A machine learning approach. Gait Posture 2022;98:34-8. [PMID: 36041285 DOI: 10.1016/j.gaitpost.2022.08.011] [Reference Citation Analysis]
5 Panza E, Meyyazhagan A, Orlacchio A. Hereditary spastic paraplegia: Genetic heterogeneity and common pathways. Exp Neurol 2022;357:114203. [PMID: 35970204 DOI: 10.1016/j.expneurol.2022.114203] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
6 Lyalina AA, Pak LA, Fisenko AP, Kondakova OB, Smirnov IE. Dystonia in children. RPJ 2021;24:112-121. [DOI: 10.46563/1560-9561-2021-24-2-112-121] [Reference Citation Analysis]