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For: Pascual B, de Bot ST, Daniels MR, França MC Jr, Toro C, Riverol M, Hedera P, Bassi MT, Bresolin N, van de Warrenburg BP, Kremer B, Nicolai J, Charles P, Xu J, Singh S, Patronas NJ, Fung SH, Gregory MD, Masdeu JC. "Ears of the Lynx" MRI Sign Is Associated with SPG11 and SPG15 Hereditary Spastic Paraplegia. AJNR Am J Neuroradiol 2019;40:199-203. [PMID: 30606727 DOI: 10.3174/ajnr.A5935] [Cited by in Crossref: 28] [Cited by in F6Publishing: 27] [Article Influence: 9.3] [Reference Citation Analysis]
Number Citing Articles
1 Mulkerrin G, França MC Jr, Lope J, Tan EL, Bede P. Neuroimaging in hereditary spastic paraplegias: from qualitative cues to precision biomarkers. Expert Rev Mol Diagn 2022. [PMID: 36042576 DOI: 10.1080/14737159.2022.2118048] [Reference Citation Analysis]
2 Utz KS, Kohl Z, Marterstock DC, Doerfler A, Winkler J, Schmidt M, Regensburger M. Neuropsychology and MRI correlates of neurodegeneration in SPG11 hereditary spastic paraplegia. Orphanet J Rare Dis 2022;17:301. [PMID: 35906604 DOI: 10.1186/s13023-022-02451-1] [Reference Citation Analysis]
3 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]
4 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]
5 Rattay TW, Schöls L, Zeltner L, Rohrschneider WK, Ernemann U, Lindig T. "Ears of the lynx" sign and thin corpus callosum on MRI in heterozygous SPG11 mutation carriers. J Neurol 2022. [PMID: 35614164 DOI: 10.1007/s00415-022-11198-5] [Reference Citation Analysis]
6 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] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Doleckova K, Roth J, Stellmachova J, Gescheidt T, Sigut V, Houska P, Jech R, Zech M, Vyhnalek M, Vyhnalkova E, Seeman P, Meszarosova AU. SPG11: clinical and genetic features of seven Czech patients and literature review. Neurological Research. [DOI: 10.1080/01616412.2021.1975224] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Daida K, Nishioka Y, Li Y, Yoshino H, Funayama M, Hattori N, Nishioka K. A complex form of hereditary spastic paraplegia harboring a novel variant, p.W1515*, in the SPG11 gene. eNeurologicalSci 2022;26:100391. [PMID: 35036589 DOI: 10.1016/j.ensci.2021.100391] [Reference Citation Analysis]
9 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 F6Publishing: 1] [Reference Citation Analysis]
10 Singh S, Israrahmed A, Mall RV, Singh V. 'Ears of the Lynx' sign: an important and useful MRI clue for diagnosis of hereditary spastic paraplegia (HSP) caused by mutation in SPG 15 gene. BMJ Case Rep 2021;14:e242275. [PMID: 34598955 DOI: 10.1136/bcr-2021-242275] [Reference Citation Analysis]
11 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: 1] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
12 Edmison D, Wang L, Gowrishankar S. Lysosome Function and Dysfunction in Hereditary Spastic Paraplegias. Brain Sci 2021;11:152. [PMID: 33498913 DOI: 10.3390/brainsci11020152] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
13 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: 13] [Article Influence: 3.0] [Reference Citation Analysis]
14 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]
15 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]
16 Wolstenholme JT, Drobná Z, Henriksen AD, Goldsby JA, Stevenson R, Irvin JW, Flaws JA, Rissman EF. Transgenerational Bisphenol A Causes Deficits in Social Recognition and Alters Postsynaptic Density Genes in Mice. Endocrinology 2019;160:1854-67. [PMID: 31188430 DOI: 10.1210/en.2019-00196] [Cited by in Crossref: 14] [Cited by in F6Publishing: 11] [Article Influence: 4.7] [Reference Citation Analysis]