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For: da Graça FF, de Rezende TJR, Vasconcellos LFR, Pedroso JL, Barsottini OGP, França MC Jr. Neuroimaging in Hereditary Spastic Paraplegias: Current Use and Future Perspectives. Front Neurol 2018;9:1117. [PMID: 30713518 DOI: 10.3389/fneur.2018.01117] [Cited by in Crossref: 23] [Cited by in F6Publishing: 17] [Article Influence: 7.7] [Reference Citation Analysis]
Number Citing Articles
1 McKenna MC, Corcia P, Couratier P, Siah WF, Pradat PF, Bede P. Frontotemporal Pathology in Motor Neuron Disease Phenotypes: Insights From Neuroimaging. Front Neurol 2021;12:723450. [PMID: 34484106 DOI: 10.3389/fneur.2021.723450] [Reference Citation Analysis]
2 Barsottini O. Lighthouse in the open sea of spastic ataxia. Parkinsonism Relat Disord 2021;91:184-5. [PMID: 34756306 DOI: 10.1016/j.parkreldis.2021.03.013] [Reference Citation Analysis]
3 Carrasco Salas P, Martínez Fernández E, Méndez Del Barrio C, Serrano Mira A, Guerrero Moreno N, Royo I, Delgado M, Oropesa JM, Vázquez Rico I. Clinical and molecular characterization of hereditary spastic paraplegia in a spanish southern region. Int J Neurosci 2020;:1-12. [PMID: 33059505 DOI: 10.1080/00207454.2020.1838514] [Cited by in Crossref: 2] [Article Influence: 1.0] [Reference Citation Analysis]
4 Giordani GM, Diniz F, Fussiger H, Gonzalez-Salazar C, Donis KC, Freua F, Ortega RPM, de Freitas JL, Barsottini OGP, Rosemberg S, Kok F, Pedroso JL, França MC Jr, Saute JAM. Clinical and molecular characterization of a large cohort of childhood onset hereditary spastic paraplegias. Sci Rep 2021;11:22248. [PMID: 34782662 DOI: 10.1038/s41598-021-01635-2] [Reference Citation Analysis]
5 Ramos-Lopes J, Ribeiro J, Laço M, Alves C, Matos A, Costa C. A De Novo BSCL2 Gene S90L Mutation in a Progressive Tetraparesis with Urinary Dysfunction and Corpus Callosum Involvement. J Pediatr Genet 2021;10:253-8. [PMID: 34504732 DOI: 10.1055/s-0040-1713768] [Reference Citation Analysis]
6 Montanaro D, Vavla M, Frijia F, Aghakhanyan G, Baratto A, Coi A, Stefan C, Girardi G, Paparella G, De Cori S, Totaro P, Lombardo F, Piccoli G, Martinuzzi A. Multimodal MRI Longitudinal Assessment of White and Gray Matter in Different SPG Types of Hereditary Spastic Paraparesis. Front Neurosci 2020;14:325. [PMID: 32581663 DOI: 10.3389/fnins.2020.00325] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
7 Bibi F, Efthymiou S, Bourinaris T, Tariq A, Zafar F, Rana N, Salpietro V, Houlden H, Raja GK, Saeed S, Minhas NM. Rare novel CYP2U1 and ZFYVE26 variants identified in two Pakistani families with spastic paraplegia. Journal of the Neurological Sciences 2020;411:116669. [DOI: 10.1016/j.jns.2020.116669] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
8 Lohkamp L, Coulter I, Ibrahim GM. Selective dorsal rhizotomy for spasticity of genetic etiology. Childs Nerv Syst 2020;36:1357-65. [DOI: 10.1007/s00381-020-04601-x] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
9 Reddy N, Doyle M, Hanagandi P, Taranath A, Dahmoush H, Krishnan P, Oztekin O, Boltshauser E, Shroff M, Mankad K. Neuroradiological Mimics of Periventricular Leukomalacia. J Child Neurol 2021;:8830738211026052. [PMID: 34937403 DOI: 10.1177/08830738211026052] [Reference Citation Analysis]
10 Panwala TF, Garcia-santibanez R, Vizcarra JA, Garcia AG, Verma S. Childhood-onset Hereditary Spastic Paraplegia (HSP): A case series and review of literature. Pediatric Neurology 2022. [DOI: 10.1016/j.pediatrneurol.2022.02.007] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
11 Brighente SF, Vicuña P, Rodrigues Louzada AL, Giordani GM, Fussiger H, Dos Santos MAR, Cubillos-Arcila DM, Winckler PB, Saute JAM. Evoked potentials as biomarkers of hereditary spastic paraplegias: A case-control study. PLoS One 2021;16:e0259397. [PMID: 34847171 DOI: 10.1371/journal.pone.0259397] [Reference Citation Analysis]
12 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: 7] [Cited by in F6Publishing: 3] [Article Influence: 7.0] [Reference Citation Analysis]
13 Navas-Sánchez FJ, Martín De Blas D, Fernández-Pena A, Alemán-Gómez Y, Lage-Castellanos A, Marcos-Vidal L, Guzmán-De-Villoria JA, Catalina I, Lillo L, Muñoz-Blanco JL, -Ugalde AO, Quintáns B, Sobrido MJ, Carmona S, Grandas F, Desco M. Corticospinal tract and motor cortex degeneration in pure hereditary spastic paraparesis type 4 (SPG4). Amyotroph Lateral Scler Frontotemporal Degener 2021;:1-10. [PMID: 34396852 DOI: 10.1080/21678421.2021.1962353] [Reference Citation Analysis]
14 Ganguly J, Jog M. Tauopathy and Movement Disorders-Unveiling the Chameleons and Mimics. Front Neurol 2020;11:599384. [PMID: 33250855 DOI: 10.3389/fneur.2020.599384] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
15 Soares IFZ, Ciarlariello VB, Feder D, Carvalho AAS. Cognitive dysfunction and psychosis: expanding the phenotype of SPG7. Neurocase 2021;:1-6. [PMID: 34003721 DOI: 10.1080/13554794.2021.1927114] [Reference Citation Analysis]
16 Servelhere KR, Rezende TJR, de Lima FD, de Brito MR, de França Nunes RF, Casseb RF, Pedroso JL, Barsottini OGP, Cendes F, França MC Jr. Brain Damage and Gene Expression Across Hereditary Spastic Paraplegia Subtypes. Mov Disord 2021;36:1644-53. [PMID: 33576112 DOI: 10.1002/mds.28519] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
17 Chhabda S, Malik P, Reddy N, Muthusamy K, Mirsky D, Sudhakar S, Mankad K. Relapsing Demyelinating Syndromes in Children: A Practical Review of Neuroradiological Mimics. Front Neurol 2020;11:627. [PMID: 32849169 DOI: 10.3389/fneur.2020.00627] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
18 Ebrahimi-Fakhari D, Teinert J, Behne R, Wimmer M, D'Amore A, Eberhardt K, Brechmann B, Ziegler M, Jensen DM, Nagabhyrava P, Geisel G, Carmody E, Shamshad U, Dies KA, Yuskaitis CJ, Salussolia CL, Ebrahimi-Fakhari D, Pearson TS, Saffari A, Ziegler A, Kölker S, Volkmann J, Wiesener A, Bearden DR, Lakhani S, Segal D, Udwadia-Hegde A, Martinuzzi A, Hirst J, Perlman S, Takiyama Y, Xiromerisiou G, Vill K, Walker WO, Shukla A, Dubey Gupta R, Dahl N, Aksoy A, Verhelst H, Delgado MR, Kremlikova Pourova R, Sadek AA, Elkhateeb NM, Blumkin L, Brea-Fernández AJ, Dacruz-Álvarez D, Smol T, Ghoumid J, Miguel D, Heine C, Schlump JU, Langen H, Baets J, Bulk S, Darvish H, Bakhtiari S, Kruer MC, Lim-Melia E, Aydinli N, Alanay Y, El-Rashidy O, Nampoothiri S, Patel C, Beetz C, Bauer P, Yoon G, Guillot M, Miller SP, Bourinaris T, Houlden H, Robelin L, Anheim M, Alamri AS, Mahmoud AAH, Inaloo S, Habibzadeh P, Faghihi MA, Jansen AC, Brock S, Roubertie A, Darras BT, Agrawal PB, Santorelli FM, Gleeson J, Zaki MS, Sheikh SI, Bennett JT, Sahin M. Defining the clinical, molecular and imaging spectrum of adaptor protein complex 4-associated hereditary spastic paraplegia. Brain 2020;143:2929-44. [PMID: 32979048 DOI: 10.1093/brain/awz307] [Cited by in Crossref: 2] [Cited by in F6Publishing: 7] [Article Influence: 2.0] [Reference Citation Analysis]
19 Lin JZ, Zheng HH, Ma QL, Wang C, Fan LP, Wu HM, Wang DN, Zhang JX, Zhan YH. Cortical Damage Associated With Cognitive and Motor Impairment in Hereditary Spastic Paraplegia: Evidence of a Novel SPAST Mutation. Front Neurol 2020;11:399. [PMID: 32536902 DOI: 10.3389/fneur.2020.00399] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
20 Menon P, Vucic S. The Upper Motor Neuron-Improved Knowledge from ALS and Related Clinical Disorders. Brain Sci 2021;11:958. [PMID: 34439577 DOI: 10.3390/brainsci11080958] [Reference Citation Analysis]
21 Bellinvia A, Pastò L, Niccolai C, Tessa A, Carrai R, Martinelli C, Moretti M, Amato MP, Santorelli FM, Sorbi S, Matà S. A new paraplegin mutation in a patient with primary progressive multiple sclerosis. Mult Scler Relat Disord 2020;44:102302. [PMID: 32570181 DOI: 10.1016/j.msard.2020.102302] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
22 Hsu SL, Chen YH, Chou CT, Chou YT, Tsai YS, Hsiao CT, Liao YC, Lee YC. Investigating ABCD1 mutations in a Taiwanese cohort with hereditary spastic paraplegia phenotype. Parkinsonism Relat Disord 2021;92:7-12. [PMID: 34649108 DOI: 10.1016/j.parkreldis.2021.10.006] [Reference Citation Analysis]
23 Pozner T, Regensburger M, Engelhorn T, Winkler J, Winner B. Janus-faced spatacsin (SPG11): involvement in neurodevelopment and multisystem neurodegeneration. Brain 2020;143:2369-79. [PMID: 32355960 DOI: 10.1093/brain/awaa099] [Cited by in Crossref: 6] [Cited by in F6Publishing: 7] [Article Influence: 3.0] [Reference Citation Analysis]
24 Lin Q, Liu Y, Ye Z, Hu J, Cai W, Weng Q, Chen WJ, Wang N, Cao D, Lin Y, Fu Y. Potential markers for sample size estimations in hereditary spastic paraplegia type 5. Orphanet J Rare Dis 2021;16:391. [PMID: 34538260 DOI: 10.1186/s13023-021-02014-w] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
25 Cosottini M, Donatelli G, Ricca I, Bianchi F, Frosini D, Montano V, Migaleddu G, Del Prete E, Tessa A, Cecchi P, D'Amelio C, Siciliano G, Mancuso M, Santorelli FM. Iron-sensitive MR imaging of the primary motor cortex to differentiate hereditary spastic paraplegia from other motor neuron diseases. Eur Radiol 2022. [PMID: 35593959 DOI: 10.1007/s00330-022-08865-6] [Reference Citation Analysis]
26 Hausman-kedem M, Ben-shachar S, Menascu S, Geva K, Sagie L, Fattal-valevski A. VPS53 gene is associated with a new phenotype of complicated hereditary spastic paraparesis. Neurogenetics 2019;20:187-95. [DOI: 10.1007/s10048-019-00586-1] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
27 Romagnoli ER, Akly MP, Miquelini LA, Funes JA, Besada CH. Hereditary spastic paraplegia: An "ears of the lynx" magnetic resonance imaging sign in a patient with recessive genetic type 11. Neuroradiol J 2021;34:42-4. [PMID: 32885726 DOI: 10.1177/1971400920953820] [Reference Citation Analysis]