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For: Darios F, Mochel F, Stevanin G. Lipids in the Physiopathology of Hereditary Spastic Paraplegias. Front Neurosci 2020;14:74. [PMID: 32180696 DOI: 10.3389/fnins.2020.00074] [Cited by in Crossref: 15] [Cited by in F6Publishing: 14] [Article Influence: 7.5] [Reference Citation Analysis]
Number Citing Articles
1 Gatti M, Magri S, Di Bella D, Sarto E, Taroni F, Mariotti C, Nanetti L. Spastic paraplegia type 46: novel and recurrent GBA2 gene variants in a compound heterozygous Italian patient with spastic ataxia phenotype. Neurol Sci 2021. [PMID: 34251556 DOI: 10.1007/s10072-021-05463-0] [Reference Citation Analysis]
2 Yahia A, Stevanin G. The History of Gene Hunting in Hereditary Spinocerebellar Degeneration: Lessons From the Past and Future Perspectives. Front Genet 2021;12:638730. [PMID: 33833777 DOI: 10.3389/fgene.2021.638730] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Darios F, Coarelli G, Durr A. Genetics in hereditary spastic paraplegias: Essential but not enough. Curr Opin Neurobiol 2021;72:8-14. [PMID: 34403957 DOI: 10.1016/j.conb.2021.07.005] [Reference Citation Analysis]
4 Godoy-corchuelo JM, Fernández-beltrán LC, Ali Z, Gil-moreno MJ, López-carbonero JI, Guerrero-sola A, Larrad-sainz A, Matias-guiu J, Matias-guiu JA, Cunningham TJ, Corrochano S. Lipid Metabolic Alterations in the ALS–FTD Spectrum of Disorders. Biomedicines 2022;10:1105. [DOI: 10.3390/biomedicines10051105] [Reference Citation Analysis]
5 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]
6 Oikawa N, Fabiano M, Müller UC, Walter J. Carboxy-terminal fragment of amyloid precursor protein mediates lipid droplet accumulation upon γ-secretase inhibition. Biochem Biophys Res Commun 2021;570:137-42. [PMID: 34280617 DOI: 10.1016/j.bbrc.2021.07.021] [Reference Citation Analysis]
7 Gunay A, Shin HH, Gozutok O, Gautam M, Ozdinler PH. Importance of lipids for upper motor neuron health and disease. Semin Cell Dev Biol 2021;112:92-104. [PMID: 33323321 DOI: 10.1016/j.semcdb.2020.11.004] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
8 Singh S, Joshi A, Kamat SS. Mapping the Neuroanatomy of ABHD16A, ABHD12, and Lysophosphatidylserines Provides New Insights into the Pathophysiology of the Human Neurological Disorder PHARC. Biochemistry 2020;59:2299-311. [PMID: 32462874 DOI: 10.1021/acs.biochem.0c00349] [Cited by in Crossref: 8] [Cited by in F6Publishing: 8] [Article Influence: 4.0] [Reference Citation Analysis]
9 Wei Q, Luo WJ, Yu H, Wang PS, Dong HL, Li HF, Wu ZY. A novel PCYT2 mutation identified in a Chinese consanguineous family with hereditary spastic paraplegia. J Genet Genomics 2021:S1673-8527(21)00192-2. [PMID: 34384721 DOI: 10.1016/j.jgg.2021.06.008] [Reference Citation Analysis]
10 Byrne DJ, Garcia-Pardo ME, Cole NB, Batnasan B, Heneghan S, Sohail A, Blackstone C, O'Sullivan NC. Liver X receptor-agonist treatment rescues degeneration in a Drosophila model of hereditary spastic paraplegia. Acta Neuropathol Commun 2022;10:40. [PMID: 35346366 DOI: 10.1186/s40478-022-01343-6] [Reference Citation Analysis]
11 Lemire G, Ito YA, Marshall AE, Chrestian N, Stanley V, Brady L, Tarnopolsky M, Curry CJ, Hartley T, Mears W, Derksen A, Rioux N, Laflamme N, Hutchison HT, Pais LS, Zaki MS, Sultan T, Dane AD, Gleeson JG, Vaz FM, Kernohan KD, Bernard G, Boycott KM; Care4Rare Canada Consortium. ABHD16A deficiency causes a complicated form of hereditary spastic paraplegia associated with intellectual disability and cerebral anomalies. Am J Hum Genet 2021;108:2017-23. [PMID: 34587489 DOI: 10.1016/j.ajhg.2021.09.005] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
12 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] [Reference Citation Analysis]
13 De Winter J, Beijer D, De Ridder W, Synofzik M, Zuchner SL, Van Damme P, Spileers W, Baets J; PREPARE consortium. PCYT2 mutations disrupting etherlipid biosynthesis: phenotypes converging on the CDP-ethanolamine pathway. Brain 2021;144:e17. [PMID: 33230519 DOI: 10.1093/brain/awaa389] [Reference Citation Analysis]
14 Elsayed LEO, Eltazi IZ, Ahmed AE, Stevanin G. Insights into Clinical, Genetic, and Pathological Aspects of Hereditary Spastic Paraplegias: A Comprehensive Overview. Front Mol Biosci 2021;8:690899. [PMID: 34901147 DOI: 10.3389/fmolb.2021.690899] [Reference Citation Analysis]
15 Ichu TA, Reed A, Ogasawara D, Ulanovskaya O, Roberts A, Aguirre CA, Bar-Peled L, Gao J, Germain J, Barbas S, Masuda K, Conti B, Tontonoz P, Cravatt BF. ABHD12 and LPCAT3 Interplay Regulates a Lyso-phosphatidylserine-C20:4 Phosphatidylserine Lipid Network Implicated in Neurological Disease. Biochemistry 2020;59:1793-9. [PMID: 32364701 DOI: 10.1021/acs.biochem.0c00292] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 3.5] [Reference Citation Analysis]
16 Tadepalle N, Rugarli EI. Lipid Droplets in the Pathogenesis of Hereditary Spastic Paraplegia. Front Mol Biosci 2021;8:673977. [PMID: 34041268 DOI: 10.3389/fmolb.2021.673977] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
17 Güner F, Pozner T, Krach F, Prots I, Loskarn S, Schlötzer-Schrehardt U, Winkler J, Winner B, Regensburger M. Axon-Specific Mitochondrial Pathology in SPG11 Alpha Motor Neurons. Front Neurosci 2021;15:680572. [PMID: 34326717 DOI: 10.3389/fnins.2021.680572] [Reference Citation Analysis]
18 Gumeni S, Vantaggiato C, Montopoli M, Orso G. Hereditary Spastic Paraplegia and Future Therapeutic Directions: Beneficial Effects of Small Compounds Acting on Cellular Stress. Front Neurosci 2021;15:660714. [PMID: 34025345 DOI: 10.3389/fnins.2021.660714] [Reference Citation Analysis]
19 Yahia A, Elsayed LEO, Valter R, Hamed AAA, Mohammed IN, Elseed MA, Salih MA, Esteves T, Auger N, Abubaker R, Koko M, Abozar F, Malik H, Adil R, Emad S, Musallam MA, Idris R, Eltazi IZM, Babai A, Ahmed EAA, Abd Allah ASI, Mairey M, Ahmed AKMA, Elbashir MI, Brice A, Ibrahim ME, Ahmed AE, Lamari F, Stevanin G. Pathogenic Variants in ABHD16A Cause a Novel Psychomotor Developmental Disorder With Spastic Paraplegia. Front Neurol 2021;12:720201. [PMID: 34489854 DOI: 10.3389/fneur.2021.720201] [Reference Citation Analysis]
20 Fowler PC, Byrne DJ, Blackstone C, O'Sullivan NC. Loss of the Mitochondrial Fission GTPase Drp1 Contributes to Neurodegeneration in a Drosophila Model of Hereditary Spastic Paraplegia. Brain Sci 2020;10:E646. [PMID: 32957716 DOI: 10.3390/brainsci10090646] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]