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For: Mathis S, Goizet C, Soulages A, Vallat JM, Masson GL. Genetics of amyotrophic lateral sclerosis: A review. J Neurol Sci 2019;399:217-26. [PMID: 30870681 DOI: 10.1016/j.jns.2019.02.030] [Cited by in Crossref: 79] [Cited by in F6Publishing: 72] [Article Influence: 26.3] [Reference Citation Analysis]
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3 Sawamura M, Imamura K, Hikawa R, Enami T, Nagahashi A, Yamakado H, Ichijo H, Fujisawa T, Yamashita H, Minamiyama S, Kaido M, Wada H, Urushitani M, Inoue H, Egawa N, Takahashi R. Cellular analysis of SOD1 protein-aggregation propensity and toxicity: a case of ALS with slow progression harboring homozygous SOD1-D92G mutation. Sci Rep 2022;12:12636. [PMID: 35879519 DOI: 10.1038/s41598-022-16871-3] [Reference Citation Analysis]
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5 Kukharsky MS, Skvortsova VI, Bachurin SO, Buchman VL. In a search for efficient treatment for amyotrophic lateral sclerosis: Old drugs for new approaches. Med Res Rev 2021;41:2804-22. [DOI: 10.1002/med.21725] [Cited by in Crossref: 4] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
6 Goodman LD, Bonini NM. New Roles for Canonical Transcription Factors in Repeat Expansion Diseases. Trends Genet 2020;36:81-92. [PMID: 31837826 DOI: 10.1016/j.tig.2019.11.003] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 2.0] [Reference Citation Analysis]
7 Hideshima M, Beck G, Yamadera M, Motoyama Y, Ikenaka K, Kakuda K, Tsuda H, Nagano S, Fujimura H, Morii E, Murayama S, Mochizuki H. A clinicopathological study of ALS with L126S mutation in the SOD1 gene presenting with isolated inferior olivary hypertrophy. Neuropathology 2020;40:191-5. [PMID: 31863610 DOI: 10.1111/neup.12620] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
8 Cristofani R, Crippa V, Cicardi ME, Tedesco B, Ferrari V, Chierichetti M, Casarotto E, Piccolella M, Messi E, Galbiati M, Rusmini P, Poletti A. A Crucial Role for the Protein Quality Control System in Motor Neuron Diseases. Front Aging Neurosci 2020;12:191. [PMID: 32792938 DOI: 10.3389/fnagi.2020.00191] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
9 Pikatza-Menoio O, Elicegui A, Bengoetxea X, Naldaiz-Gastesi N, López de Munain A, Gerenu G, Gil-Bea FJ, Alonso-Martín S. The Skeletal Muscle Emerges as a New Disease Target in Amyotrophic Lateral Sclerosis. J Pers Med 2021;11:671. [PMID: 34357138 DOI: 10.3390/jpm11070671] [Reference Citation Analysis]
10 Pecoraro V, Mandrioli J, Carone C, Chiò A, Traynor BJ, Trenti T. The NGS technology for the identification of genes associated with the ALS. A systematic review. Eur J Clin Invest 2020;50:e13228. [PMID: 32293029 DOI: 10.1111/eci.13228] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
11 Karagiannis P, Inoue H. ALS, a cellular whodunit on motor neuron degeneration. Mol Cell Neurosci 2020;107:103524. [PMID: 32629110 DOI: 10.1016/j.mcn.2020.103524] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
12 Huang F, Zhu Y, Hsiao-Nakamoto J, Tang X, Dugas JC, Moscovitch-Lopatin M, Glass JD, Brown RH Jr, Ladha SS, Lacomis D, Harris JM, Scearce-Levie K, Ho C, Bowser R, Berry JD. Longitudinal biomarkers in amyotrophic lateral sclerosis. Ann Clin Transl Neurol 2020;7:1103-16. [PMID: 32515902 DOI: 10.1002/acn3.51078] [Cited by in Crossref: 10] [Cited by in F6Publishing: 9] [Article Influence: 5.0] [Reference Citation Analysis]
13 Kaku H, Ludlow AV, Gutknecht MF, Rothstein TL. FAIM Opposes Aggregation of Mutant SOD1 That Typifies Some Forms of Familial Amyotrophic Lateral Sclerosis. Front Neurosci 2020;14:110. [PMID: 32153351 DOI: 10.3389/fnins.2020.00110] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
14 Goldsmith J, Holzbaur ELF. Presynaptic Homeostatic Plasticity Staves off Neurodegenerative Pathophysiology up to a Tipping Point. Neuron 2020;107:6-8. [PMID: 32645308 DOI: 10.1016/j.neuron.2020.06.013] [Reference Citation Analysis]
15 Magota H, Sasaki M, Kataoka-Sasaki Y, Oka S, Ukai R, Kiyose R, Onodera R, Kocsis JD, Honmou O. Intravenous infusion of mesenchymal stem cells delays disease progression in the SOD1G93A transgenic amyotrophic lateral sclerosis rat model. Brain Res 2021;1757:147296. [PMID: 33516815 DOI: 10.1016/j.brainres.2021.147296] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
16 Chang KH, Chen CM. The Role of Oxidative Stress in Parkinson's Disease. Antioxidants (Basel) 2020;9:E597. [PMID: 32650609 DOI: 10.3390/antiox9070597] [Cited by in Crossref: 19] [Cited by in F6Publishing: 14] [Article Influence: 9.5] [Reference Citation Analysis]
17 Azoulay-Ginsburg S, Di Salvio M, Weitman M, Afri M, Ribeiro S, Ebbinghaus S, Cestra G, Gruzman A. Chemical chaperones targeted to the endoplasmic reticulum (ER) and lysosome prevented neurodegeneration in a C9orf72 repeat expansion drosophila amyotrophic lateral sclerosis (ALS) model. Pharmacol Rep 2021;73:536-50. [PMID: 33661518 DOI: 10.1007/s43440-021-00226-2] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
18 Jin M, Akgün K, Ziemssen T, Kipp M, Günther R, Hermann A. Interleukin-17 and Th17 Lymphocytes Directly Impair Motoneuron Survival of Wildtype and FUS-ALS Mutant Human iPSCs. Int J Mol Sci 2021;22:8042. [PMID: 34360808 DOI: 10.3390/ijms22158042] [Reference Citation Analysis]
19 Mouzat K, Chudinova A, Polge A, Kantar J, Camu W, Raoul C, Lumbroso S. Regulation of Brain Cholesterol: What Role Do Liver X Receptors Play in Neurodegenerative Diseases? Int J Mol Sci 2019;20:E3858. [PMID: 31398791 DOI: 10.3390/ijms20163858] [Cited by in Crossref: 20] [Cited by in F6Publishing: 19] [Article Influence: 6.7] [Reference Citation Analysis]
20 Wendebourg MJ, Kuhle J, Hardmeier M. Case Report: A 72-Year-Old Woman With Progressive Motor Weakness, Dry Eyes and High Levels of Serum Neurofilament Light Chain. Front Neurol 2022;13:889894. [DOI: 10.3389/fneur.2022.889894] [Reference Citation Analysis]
21 Capece G, Ceroni M, Alfonsi E, Palmieri I, Cereda C, Diamanti L. Case Report: Laryngospasm as Initial Manifestation of Amyotrophic Lateral Sclerosis in a Long-Survival Patient With Heterozygous p.D90A - SOD1 Mutation. Front Neurol 2021;12:708885. [PMID: 34659083 DOI: 10.3389/fneur.2021.708885] [Reference Citation Analysis]
22 Rusmini P, Cristofani R, Tedesco B, Ferrari V, Messi E, Piccolella M, Casarotto E, Chierichetti M, Cicardi ME, Galbiati M, Geroni C, Lombardi P, Crippa V, Poletti A. Enhanced Clearance of Neurotoxic Misfolded Proteins by the Natural Compound Berberine and Its Derivatives. Int J Mol Sci 2020;21:E3443. [PMID: 32414108 DOI: 10.3390/ijms21103443] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
23 Ueda T, Ito T, Kurita H, Inden M, Hozumi I. p-Coumaric Acid Has Protective Effects against Mutant Copper-Zinc Superoxide Dismutase 1 via the Activation of Autophagy in N2a Cells. Int J Mol Sci 2019;20:E2942. [PMID: 31208129 DOI: 10.3390/ijms20122942] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.7] [Reference Citation Analysis]
24 Mitsui S, Otomo A, Sato K, Ishiyama M, Shimakura K, Okada-yamaguchi C, Warabi E, Yanagawa T, Aoki M, Shang H, Hadano S. SQSTM1, a protective factor of SOD1-linked motor neuron disease, regulates the accumulation and distribution of ubiquitinated protein aggregates in neuron. Neurochemistry International 2022. [DOI: 10.1016/j.neuint.2022.105364] [Reference Citation Analysis]
25 Wang XL, Feng ST, Wang ZZ, Chen NH, Zhang Y. Role of mitophagy in mitochondrial quality control: Mechanisms and potential implications for neurodegenerative diseases. Pharmacol Res 2021;165:105433. [PMID: 33454337 DOI: 10.1016/j.phrs.2021.105433] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
26 Fiondella L, Cavallieri F, Canali E, Cabboi MP, Marti A, Sireci F, Fiocchi A, Montanari G, Montepietra S, Valzania F. Co-Occurrence of Multiple Sclerosis and Amyotrophic Lateral Sclerosis in an FUS-Mutated Patient: A Case Report. Brain Sciences 2022;12:531. [DOI: 10.3390/brainsci12050531] [Reference Citation Analysis]
27 Ueda T, Ito T, Inden M, Kurita H, Yamamoto A, Hozumi I. Stem Cells From Human Exfoliated Deciduous Teeth-Conditioned Medium (SHED-CM) is a Promising Treatment for Amyotrophic Lateral Sclerosis. Front Pharmacol 2022;13:805379. [DOI: 10.3389/fphar.2022.805379] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
28 Gregory JM, McDade K, Livesey MR, Croy I, Marion de Proce S, Aitman T, Chandran S, Smith C. Spatial transcriptomics identifies spatially dysregulated expression of GRM3 and USP47 in amyotrophic lateral sclerosis. Neuropathol Appl Neurobiol 2020;46:441-57. [PMID: 31925813 DOI: 10.1111/nan.12597] [Cited by in Crossref: 7] [Cited by in F6Publishing: 6] [Article Influence: 3.5] [Reference Citation Analysis]
29 Gromicho M, Coutinho AM, Pronto-laborinho AC, Raposeiro R, Tavares J, Antunes D, de Carvalho M. Targeted next-generation sequencing study in familial ALS-FTD Portuguese patients negative for C9orf72 HRE. J Neurol 2020;267:3578-92. [DOI: 10.1007/s00415-020-10042-y] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
30 Peng J, Pan J, Mo J, Peng Y, Rai SN. MPO/HOCl Facilitates Apoptosis and Ferroptosis in the SOD1G93A Motor Neuron of Amyotrophic Lateral Sclerosis. Oxidative Medicine and Cellular Longevity 2022;2022:1-19. [DOI: 10.1155/2022/8217663] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 3.0] [Reference Citation Analysis]
31 Morello G, Gentile G, Spataro R, Spampinato AG, Guarnaccia M, Salomone S, La Bella V, Conforti FL, Cavallaro S. Genomic Portrait of a Sporadic Amyotrophic Lateral Sclerosis Case in a Large Spinocerebellar Ataxia Type 1 Family. J Pers Med 2020;10:E262. [PMID: 33276461 DOI: 10.3390/jpm10040262] [Reference Citation Analysis]
32 Lieberman RL, Ma MT. Molecular Insights into Myocilin and Its Glaucoma-Causing Misfolded Olfactomedin Domain Variants. Acc Chem Res 2021;54:2205-15. [PMID: 33847483 DOI: 10.1021/acs.accounts.1c00060] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
33 Lum JS, Brown ML, Farrawell NE, McAlary L, Ly D, Chisholm CG, Snow J, Vine KL, Karl T, Kreilaus F, McInnes LE, Nikseresht S, Donnelly PS, Crouch PJ, Yerbury JJ. CuATSM improves motor function and extends survival but is not tolerated at a high dose in SOD1G93A mice with a C57BL/6 background. Sci Rep 2021;11:19392. [PMID: 34588483 DOI: 10.1038/s41598-021-98317-w] [Reference Citation Analysis]
34 Root J, Merino P, Nuckols A, Johnson M, Kukar T. Lysosome dysfunction as a cause of neurodegenerative diseases: Lessons from frontotemporal dementia and amyotrophic lateral sclerosis. Neurobiol Dis 2021;154:105360. [PMID: 33812000 DOI: 10.1016/j.nbd.2021.105360] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 6.0] [Reference Citation Analysis]
35 Smukowski SN, Maioli H, Latimer CS, Bird TD, Jayadev S, Valdmanis PN. Progress in Amyotrophic Lateral Sclerosis Gene Discovery: Reflecting on Classic Approaches and Leveraging Emerging Technologies. Neurol Genet 2022;8:e669. [PMID: 35620141 DOI: 10.1212/NXG.0000000000000669] [Reference Citation Analysis]
36 Zhao G, Liu Z, Wang M, Yuan Y, Ni J, Li W, Huang L, Hu Y, Liu P, Hou X, Guo J, Jiang H, Shen L, Tang B, Li J, Wang J. Gene4MND: An Integrative Genetic Database and Analytic Platform for Motor Neuron Disease. Front Mol Neurosci 2021;14:644202. [PMID: 33867934 DOI: 10.3389/fnmol.2021.644202] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
37 Fernández-Cruz I, Reynaud E. Proteasome Subunits Involved in Neurodegenerative Diseases. Arch Med Res 2021;52:1-14. [PMID: 32962866 DOI: 10.1016/j.arcmed.2020.09.007] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
38 Gittings LM, Sattler R. Recent advances in understanding amyotrophic lateral sclerosis and emerging therapies. Fac Rev 2020;9:12. [PMID: 33659944 DOI: 10.12703/b/9-12] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
39 Ni J, Liu Z, Li W, Yuan Y, Huang L, Hu Y, Liu P, Hou X, Jiao B, Li J, Shen L, Jiang H, Tang B, Wang J. Rare, pathogenic variants in LRP10 are associated with amyotrophic lateral sclerosis in patients from mainland China. Neurobiol Aging 2021;97:145.e17-22. [PMID: 32690342 DOI: 10.1016/j.neurobiolaging.2020.06.013] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
40 Mol MO, Wong TH, Melhem S, Basu S, Viscusi R, Galjart N, Rozemuller AJM, Fallini C, Landers JE, Kaat LD, Seelaar H, van Rooij JGJ, van Swieten JC. Novel TUBA4A Variant Associated With Familial Frontotemporal Dementia. Neurol Genet 2021;7:e596. [PMID: 34169147 DOI: 10.1212/NXG.0000000000000596] [Reference Citation Analysis]
41 Soldatov VO, Kukharsky MS, Belykh AE, Sobolev AM, Deykin AV. Retinal Damage in Amyotrophic Lateral Sclerosis: Underlying Mechanisms. Eye Brain 2021;13:131-46. [PMID: 34012311 DOI: 10.2147/EB.S299423] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
42 Cappella M, Ciotti C, Cohen-Tannoudji M, Biferi MG. Gene Therapy for ALS-A Perspective. Int J Mol Sci 2019;20:E4388. [PMID: 31500113 DOI: 10.3390/ijms20184388] [Cited by in Crossref: 34] [Cited by in F6Publishing: 33] [Article Influence: 11.3] [Reference Citation Analysis]
43 Darbà J. Current status and direct medical cost of amyotrophic lateral sclerosis in the region of Catalonia: A population-based analysis. PLoS One 2019;14:e0223772. [PMID: 31603947 DOI: 10.1371/journal.pone.0223772] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.7] [Reference Citation Analysis]
44 Violi F, Solovyev N, Vinceti M, Mandrioli J, Lucio M, Michalke B. The study of levels from redox-active elements in cerebrospinal fluid of amyotrophic lateral sclerosis patients carrying disease-related gene mutations shows potential copper dyshomeostasis. Metallomics 2020;12:668-81. [PMID: 32373852 DOI: 10.1039/d0mt00051e] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 8.0] [Reference Citation Analysis]
45 Büyüköz M, Sazci A, Ergül E, Idrisoglu HA. Investigation of some variations of superoxide dismutase gene family in Turkish sporadic amyotrophic lateral sclerosis patients. Brain Disorders 2021;3:100013. [DOI: 10.1016/j.dscb.2021.100013] [Reference Citation Analysis]
46 Parakh S, Atkin JD. The Mitochondrial-associated ER membrane (MAM) compartment and its dysregulation in Amyotrophic Lateral Sclerosis (ALS). Semin Cell Dev Biol 2021;112:105-13. [PMID: 33707063 DOI: 10.1016/j.semcdb.2021.02.002] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
47 Liu Z, Yuan Y, Wang M, Ni J, Li W, Huang L, Hu Y, Liu P, Hou X, Hou X, Du J, Weng L, Zhang R, Niu Q, Tang J, Jiang H, Shen L, Tang B, Wang J. Mutation spectrum of amyotrophic lateral sclerosis in Central South China. Neurobiol Aging 2021:S0197-4580(21)00202-5. [PMID: 34275688 DOI: 10.1016/j.neurobiolaging.2021.06.008] [Reference Citation Analysis]
48 Fleming A, Bourdenx M, Fujimaki M, Karabiyik C, Krause GJ, Lopez A, Martín-Segura A, Puri C, Scrivo A, Skidmore J, Son SM, Stamatakou E, Wrobel L, Zhu Y, Cuervo AM, Rubinsztein DC. The different autophagy degradation pathways and neurodegeneration. Neuron 2022:S0896-6273(22)00056-3. [PMID: 35134347 DOI: 10.1016/j.neuron.2022.01.017] [Cited by in Crossref: 10] [Cited by in F6Publishing: 8] [Article Influence: 10.0] [Reference Citation Analysis]
49 Swindell WR, Kruse CPS, List EO, Berryman DE, Kopchick JJ. ALS blood expression profiling identifies new biomarkers, patient subgroups, and evidence for neutrophilia and hypoxia. J Transl Med 2019;17:170. [PMID: 31118040 DOI: 10.1186/s12967-019-1909-0] [Cited by in Crossref: 15] [Cited by in F6Publishing: 14] [Article Influence: 5.0] [Reference Citation Analysis]
50 Lehky T, Grunseich C. Juvenile Amyotrophic Lateral Sclerosis: A Review. Genes (Basel) 2021;12:1935. [PMID: 34946884 DOI: 10.3390/genes12121935] [Reference Citation Analysis]
51 Andrew A, Zhou J, Gui J, Harrison A, Shi X, Li M, Guetti B, Nathan R, Tischbein M, Pioro EP, Stommel E, Bradley W. Pesticides applied to crops and amyotrophic lateral sclerosis risk in the U.S. Neurotoxicology 2021;87:128-35. [PMID: 34562505 DOI: 10.1016/j.neuro.2021.09.004] [Reference Citation Analysis]
52 Tipton MJ, Corbett J, Eglin CM, Mekjavic IB, Montgomery H. In pursuit of the unicorn. Exp Physiol 2021;106:385-8. [PMID: 33174651 DOI: 10.1113/EP089147] [Reference Citation Analysis]
53 van Bruggen R, Maksimovic K, You J, Tran DD, Lee HJ, Khan M, Kao CS, Kim JR, Cho W, Chen XXL, Park J. MATR3 F115C knock-in mice do not exhibit motor defects or neuropathological features of ALS. Biochem Biophys Res Commun 2021;568:48-54. [PMID: 34182213 DOI: 10.1016/j.bbrc.2021.06.052] [Reference Citation Analysis]
54 Zhang J, Qiu W, Hu F, Zhang X, Deng Y, Nie H, Xu R. The rs2619566, rs10260404, and rs79609816 Polymorphisms Are Associated With Sporadic Amyotrophic Lateral Sclerosis in Individuals of Han Ancestry From Mainland China. Front Genet 2021;12:679204. [PMID: 34421992 DOI: 10.3389/fgene.2021.679204] [Reference Citation Analysis]
55 Wobst HJ, Mack KL, Brown DG, Brandon NJ, Shorter J. The clinical trial landscape in amyotrophic lateral sclerosis-Past, present, and future. Med Res Rev 2020;40:1352-84. [PMID: 32043626 DOI: 10.1002/med.21661] [Cited by in Crossref: 18] [Cited by in F6Publishing: 16] [Article Influence: 9.0] [Reference Citation Analysis]
56 Bernard E, Pegat A, Svahn J, Bouhour F, Leblanc P, Millecamps S, Thobois S, Guissart C, Lumbroso S, Mouzat K. Clinical and Molecular Landscape of ALS Patients with SOD1 Mutations: Novel Pathogenic Variants and Novel Phenotypes. A Single ALS Center Study. Int J Mol Sci 2020;21:E6807. [PMID: 32948071 DOI: 10.3390/ijms21186807] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 1.5] [Reference Citation Analysis]
57 La Cognata V, Golini E, Iemmolo R, Balletta S, Morello G, De Rosa C, Villari A, Marinelli S, Vacca V, Bonaventura G, Dell'Albani P, Aronica E, Mammano F, Mandillo S, Cavallaro S. CXCR2 increases in ALS cortical neurons and its inhibition prevents motor neuron degeneration in vitro and improves neuromuscular function in SOD1G93A mice. Neurobiol Dis 2021;160:105538. [PMID: 34743985 DOI: 10.1016/j.nbd.2021.105538] [Reference Citation Analysis]
58 Jia R, Chen Q, Zhou Q, Zhang R, Jin J, Hu F, Liu X, Qin X, Kang L, Zhao S, Dang Y, Dang J. Characteristics of serum metabolites in sporadic amyotrophic lateral sclerosis patients based on gas chromatography-mass spectrometry. Sci Rep 2021;11:20786. [PMID: 34675267 DOI: 10.1038/s41598-021-00312-8] [Reference Citation Analysis]
59 Feng F, Wang H, Liu J, Wang Z, Xu B, Zhao K, Tao X, He Z, Yang F, Huang X. Genetic and clinical features of Chinese sporadic amyotrophic lateral sclerosis patients with TARDBP mutations. Brain Behav 2021. [PMID: 34333853 DOI: 10.1002/brb3.2312] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
60 Bassola B, Lizio A, Lucchini M, Sansone VA, Lusignani M. Development and Validation of the Self-care in Motor Neuron Disease Index. J Neurosci Nurs 2019;51:325-30. [PMID: 31626077 DOI: 10.1097/JNN.0000000000000473] [Reference Citation Analysis]
61 Le Gall L, Anakor E, Connolly O, Vijayakumar UG, Duddy WJ, Duguez S. Molecular and Cellular Mechanisms Affected in ALS. J Pers Med 2020;10:E101. [PMID: 32854276 DOI: 10.3390/jpm10030101] [Cited by in Crossref: 13] [Cited by in F6Publishing: 14] [Article Influence: 6.5] [Reference Citation Analysis]
62 Sai Swaroop R, Akhil PS, Sai Sanwid P, Bandana P, Raksha RK, Meghana M, Bibha C, Sivaramakrishnan V. Integrated multi-omic data analysis and validation with yeast model show oxidative phosphorylation modulates protein aggregation in amyotrophic lateral sclerosis. J Biomol Struct Dyn 2022;:1-20. [PMID: 35749136 DOI: 10.1080/07391102.2022.2090441] [Reference Citation Analysis]
63 Barp A, Gerardi F, Lizio A, Sansone VA, Lunetta C. Emerging Drugs for the Treatment of Amyotrophic Lateral Sclerosis: A Focus on Recent Phase 2 Trials. Expert Opin Emerg Drugs 2020;25:145-64. [PMID: 32456491 DOI: 10.1080/14728214.2020.1769067] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
64 Abdul Aziz NA, Toh T, Goh K, Loh E, Capelle DP, Abdul Latif L, Leow AH, Yim CC, Zainal Abidin MF, Ruslan SR, Shahrizaila N. Natural history and clinical features of ALS in Malaysia. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 2021;22:108-16. [DOI: 10.1080/21678421.2020.1832121] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
65 Ma J, Pang X, Huang S, Zhang J, Wang J, Zhao R, Chang X, Guo J, Zhang W. Genetic analysis in Chinese patients with familial or young-onset amyotrophic lateral sclerosis. Neurol Sci 2021. [PMID: 34564799 DOI: 10.1007/s10072-021-05634-z] [Reference Citation Analysis]
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