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For: Beaudin M, Matilla-Dueñas A, Soong BW, Pedroso JL, Barsottini OG, Mitoma H, Tsuji S, Schmahmann JD, Manto M, Rouleau GA, Klein C, Dupre N. The Classification of Autosomal Recessive Cerebellar Ataxias: a Consensus Statement from the Society for Research on the Cerebellum and Ataxias Task Force. Cerebellum 2019;18:1098-125. [PMID: 31267374 DOI: 10.1007/s12311-019-01052-2] [Cited by in Crossref: 37] [Cited by in F6Publishing: 24] [Article Influence: 18.5] [Reference Citation Analysis]
Number Citing Articles
1 Paulus-Andres JA, Burnett MS. Three Adult-Onset Autosomal Recessive Ataxias: What Adult Neurologists Need to Know. Neurol Clin Pract 2021;11:256-62. [PMID: 34484893 DOI: 10.1212/CPJ.0000000000000947] [Reference Citation Analysis]
2 Rydning SL, Wedding IM. Monogenic mysteries unravel mitochondrial mechanisms. Brain 2021;144:1286-8. [PMID: 33712815 DOI: 10.1093/brain/awab098] [Reference Citation Analysis]
3 Gannamani R, van der Veen S, van Egmond M, de Koning TJ, Tijssen MAJ. Challenges in Clinicogenetic Correlations: One Phenotype - Many Genes. Mov Disord Clin Pract 2021;8:311-21. [PMID: 33816658 DOI: 10.1002/mdc3.13163] [Cited by in Crossref: 3] [Article Influence: 3.0] [Reference Citation Analysis]
4 Cocozza S, Pontillo G, De Michele G, Di Stasi M, Guerriero E, Perillo T, Pane C, De Rosa A, Ugga L, Brunetti A. Conventional MRI findings in hereditary degenerative ataxias: a pictorial review. Neuroradiology 2021;63:983-99. [PMID: 33733696 DOI: 10.1007/s00234-021-02682-2] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
5 Pedroso JL, de Rezende Pinto WBV, Barsottini OGP, Oliveira ASB. Should we investigate mitochondrial disorders in progressive adult-onset undetermined ataxias? Cerebellum Ataxias 2020;7:13. [PMID: 32922825 DOI: 10.1186/s40673-020-00122-0] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
6 Angelini C, Meissner W, Goizet C. Atassie cerebellari ereditarie. EMC - Neurologia 2021;21:1-14. [DOI: 10.1016/s1634-7072(21)45784-3] [Reference Citation Analysis]
7 Haj Salem I, Beaudin M, Stumpf M, Estiar MA, Côté PO, Brunet F, Gamache PL, Rouleau GA, Mourabit-Amari K, Gan-Or Z, Dupré N. Genetic and Epidemiological Study of Adult Ataxia and Spastic Paraplegia in Eastern Quebec. Can J Neurol Sci 2021;48:655-65. [PMID: 33397523 DOI: 10.1017/cjn.2020.277] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
8 Beaudin M, Manto M, Schmahmann JD, Pandolfo M, Dupre N. Recessive cerebellar and afferent ataxias - clinical challenges and future directions. Nat Rev Neurol 2022. [PMID: 35332317 DOI: 10.1038/s41582-022-00634-9] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
9 Phang MWL, Lew SY, Chung I, Lim WK, Lim LW, Wong KH. Therapeutic roles of natural remedies in combating hereditary ataxia: A systematic review. Chin Med 2021;16:15. [PMID: 33509239 DOI: 10.1186/s13020-020-00414-x] [Reference Citation Analysis]
10 Mutlu-Albayrak H, Kırat E, Gürbüz G. Childhood-onset autosomal recessive ataxias: a cross-sectional study from Turkey. Neurogenetics 2020;21:59-66. [PMID: 31741144 DOI: 10.1007/s10048-019-00597-y] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
11 Krygier M, Mazurkiewicz-Bełdzińska M. Milestones in genetics of cerebellar ataxias. Neurogenetics 2021. [PMID: 34224032 DOI: 10.1007/s10048-021-00656-3] [Reference Citation Analysis]
12 Vidhale TA, Gupta HR, Pj R, Gandhi C. Very late-onset Friedreich's ataxia with rapid course mimicking as possible multiple system atrophy cerebellar type. BMJ Case Rep 2021;14:e242073. [PMID: 34301694 DOI: 10.1136/bcr-2021-242073] [Reference Citation Analysis]
13 Bogdanova-Mihaylova P, Plapp HM, Chen H, Early A, Cassidy L, Walsh RA, Murphy SM. Longitudinal Assessment Using Optical Coherence Tomography in Patients with Friedreich's Ataxia. Tomography 2021;7:915-31. [PMID: 34941648 DOI: 10.3390/tomography7040076] [Reference Citation Analysis]
14 Saida K, Tamaoki J, Sasaki M, Haniffa M, Koshimizu E, Sengoku T, Maeda H, Kikuchi M, Yokoyama H, Sakamoto M, Iwama K, Sekiguchi F, Hamanaka K, Fujita A, Mizuguchi T, Ogata K, Miyake N, Miyatake S, Kobayashi M, Matsumoto N. Pathogenic variants in the survival of motor neurons complex gene GEMIN5 cause cerebellar atrophy. Clin Genet 2021;100:722-30. [PMID: 34569062 DOI: 10.1111/cge.14066] [Reference Citation Analysis]
15 Parvez MSA, Ohtsuki G. Acute Cerebellar Inflammation and Related Ataxia: Mechanisms and Pathophysiology. Brain Sciences 2022;12:367. [DOI: 10.3390/brainsci12030367] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
16 Raslan IR, Barsottini OG, Pedroso JL. A Proposed Clinical Classification and a Diagnostic Approach for Congenital Ataxias. Neurol Clin Pract 2021;11:e328-36. [PMID: 34484907 DOI: 10.1212/CPJ.0000000000000966] [Reference Citation Analysis]
17 Benussi A, Cantoni V, Manes M, Libri I, Dell'Era V, Datta A, Thomas C, Ferrari C, Di Fonzo A, Fancellu R, Grassi M, Brusco A, Alberici A, Borroni B. Motor and cognitive outcomes of cerebello-spinal stimulation in neurodegenerative ataxia. Brain 2021:awab157. [PMID: 33950222 DOI: 10.1093/brain/awab157] [Reference Citation Analysis]
18 Şen Ö, Emanet M, Marino A, Belenli Gümüş M, Bartolucci M, Doccini S, Catalano F, Genchi GG, Santorelli FM, Petretto A, Ciofani G. Evaluation of the therapeutic potential of resveratrol-loaded nanostructured lipid carriers on autosomal recessive spastic ataxia of Charlevoix-Saguenay patient-derived fibroblasts. Materials & Design 2021;209:110012. [DOI: 10.1016/j.matdes.2021.110012] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 4.0] [Reference Citation Analysis]
19 Santos M, Damásio J, Kun-Rodrigues C, Barbot C, Sequeiros J, Brás J, Alonso I, Guerreiro R. Novel MAG Variant Causes Cerebellar Ataxia with Oculomotor Apraxia: Molecular Basis and Expanded Clinical Phenotype. J Clin Med 2020;9:E1212. [PMID: 32340215 DOI: 10.3390/jcm9041212] [Reference Citation Analysis]
20 Dragašević-Mišković N, Stanković I, Milovanović A, Kostić VS. Autosomal recessive adult onset ataxia. J Neurol 2021. [PMID: 34499204 DOI: 10.1007/s00415-021-10763-8] [Reference Citation Analysis]
21 Lew SY, Phang MWL, Chong PS, Roy J, Poon CH, Yu WS, Lim LW, Wong KH. Discovery of Therapeutics Targeting Oxidative Stress in Autosomal Recessive Cerebellar Ataxia: A Systematic Review. Pharmaceuticals (Basel) 2022;15:764. [PMID: 35745683 DOI: 10.3390/ph15060764] [Reference Citation Analysis]
22 Rudenskaya GE, Kadnikova VA, Ryzhkova OP. [Spastic ataxia of Charlevoix-Saguenay: the first Russian case report and literature review]. Zh Nevrol Psikhiatr Im S S Korsakova 2020;120:85-91. [PMID: 32307416 DOI: 10.17116/jnevro202012002185] [Reference Citation Analysis]
23 Quelle-Regaldie A, Sobrido-Cameán D, Barreiro-Iglesias A, Sobrido MJ, Sánchez L. Zebrafish Models of Autosomal Recessive Ataxias. Cells 2021;10:836. [PMID: 33917666 DOI: 10.3390/cells10040836] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
24 Mitoma H, Manto M, Gandini J. Recent Advances in the Treatment of Cerebellar Disorders. Brain Sci 2019;10:E11. [PMID: 31878024 DOI: 10.3390/brainsci10010011] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 0.7] [Reference Citation Analysis]
25 Perlman SL. Update on the Treatment of Ataxia: Medication and Emerging Therapies. Neurotherapeutics 2020;17:1660-4. [PMID: 33021724 DOI: 10.1007/s13311-020-00941-3] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
26 Martínez-martín Á, García-garcía J, Díaz-maroto Cicuéndez I, Quintanilla-mata M, Segura T. Bringing light into the darkness: autosomal recessive cerebellar ataxia due to a recessive mutation in the SEPSECS gene. Neurología (English Edition) 2022. [DOI: 10.1016/j.nrleng.2022.01.002] [Reference Citation Analysis]
27 Cheillan D. Zellweger Syndrome Disorders: From Severe Neonatal Disease to Atypical Adult Presentation. Adv Exp Med Biol 2020;1299:71-80. [PMID: 33417208 DOI: 10.1007/978-3-030-60204-8_6] [Reference Citation Analysis]
28 Baty K, Farrugia ME, Hopton S, Falkous G, Schaefer AM, Stewart W, Willison HJ, Reilly MM, Blakely EL, Taylor RW, Ng YS. A novel MT-CO2 variant causing cerebellar ataxia and neuropathy: The role of muscle biopsy in diagnosis and defining pathogenicity. Neuromuscul Disord 2021:S0960-8966(21)00139-5. [PMID: 34325999 DOI: 10.1016/j.nmd.2021.05.014] [Reference Citation Analysis]
29 Klockgether T, Ashizawa T, Brais B, Chuang R, Durr A, Fogel B, Greenfield J, Hagen S, Jardim LB, Jiang H, Onodera O, Pedroso JL, Soong BW, Szmulewicz D, Graessner H, Synofzik M; Ataxia Global Initiative (AGI). Paving the Way Toward Meaningful Trials in Ataxias: An Ataxia Global Initiative Perspective. Mov Disord 2022. [PMID: 35475582 DOI: 10.1002/mds.29032] [Reference Citation Analysis]
30 Christen M, Högler S, Kleiter M, Leschnik M, Weber C, Thaller D, Jagannathan V, Leeb T. Deletion of the SELENOP gene leads to CNS atrophy with cerebellar ataxia in dogs. PLoS Genet 2021;17:e1009716. [PMID: 34339417 DOI: 10.1371/journal.pgen.1009716] [Reference Citation Analysis]
31 Gandini J, Manto M, Bremova-ertl T, Feil K, Strupp M. The neurological update: therapies for cerebellar ataxias in 2020. J Neurol 2020;267:1211-20. [DOI: 10.1007/s00415-020-09717-3] [Cited by in Crossref: 10] [Cited by in F6Publishing: 7] [Article Influence: 5.0] [Reference Citation Analysis]
32 Aguillon D, VasquezMadrigal DL, Moreno S, Hernández D, Isaza-Ruget M, Lopez JJ, Landires I, Nuñez-Samudio V, Restrepo CM, Vidal OM, Vélez JI, Arcos-Holzinger M, Lopera F, Arcos-Burgos M. Ataxia with Ocular Apraxia Type 1 (AOA1) (APTX, W279* Mutation): Neurological, Neuropsychological, and Molecular Outlining of a Heterogenous Phenotype in Four Colombian Siblings. Mol Neurobiol 2022. [PMID: 35420381 DOI: 10.1007/s12035-022-02821-7] [Reference Citation Analysis]
33 Iodice A, Spagnoli C, Cangini M, Soliani L, Rizzi S, Salerno GG, Frattini D, Pisani F, Fusco C. Long-term follow-up in infantile-onset SCAR18: A case report. J Clin Neurosci 2020;77:232-4. [PMID: 32387255 DOI: 10.1016/j.jocn.2020.05.008] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
34 Zhao J, Zhang H, Fan X, Yu X, Huai J. Lipid Dyshomeostasis and Inherited Cerebellar Ataxia. Mol Neurobiol 2022. [PMID: 35420383 DOI: 10.1007/s12035-022-02826-2] [Reference Citation Analysis]
35 Mascalchi M. MRI CNS Atrophy Pattern and the Etiologies of Progressive Ataxias. Tomography 2022;8:423-37. [DOI: 10.3390/tomography8010035] [Reference Citation Analysis]
36 Guissart C, Harrison AN, Benkirane M, Oncel I, Arslan EA, Chassevent AK., Baraῆano K, Larrieu L, Iascone M, Tenconi R, Claustres M, Eroglu-ertugrul N, Calvas P, Topaloglu H, Molday RS, Koenig M. ATP8A2-related disorders as recessive cerebellar ataxia. J Neurol 2020;267:203-13. [DOI: 10.1007/s00415-019-09579-4] [Cited by in Crossref: 5] [Cited by in F6Publishing: 4] [Article Influence: 1.7] [Reference Citation Analysis]
37 Kinkar JS, Jameel PZ, Kumawat BL, Kalbhor P. Heterozygous deletion in exon 6 of STEX gene causing ataxia with oculomotor apraxia type 2 (AOA-2) with ovarian failure. BMJ Case Rep 2021;14:e241767. [PMID: 34193451 DOI: 10.1136/bcr-2021-241767] [Reference Citation Analysis]
38 Habibzadeh P, Tabatabaei Z, Inaloo S, Nashatizadeh MM, Synofzik M, Ostovan VR, Faghihi MA. Case Report: Expanding the Genetic and Phenotypic Spectrum of Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay. Front Genet 2020;11:585136. [PMID: 33414805 DOI: 10.3389/fgene.2020.585136] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
39 Gama MTD, Braga-Neto P, Rangel DM, Godeiro C Jr, Alencar R, Embiruçu EK, Cornejo-Olivas M, Sarapura-Castro E, Saffie Awad P, Muñoz Chesta D, Kauffman M, Rodriguez-Quiroga S, Jardim LB, da Graça FF, França MC Jr, Tomaselli PJ, Marques W Jr, Teive HAG, Barsottini OGP, Pedroso JL, Synofzik M. Autosomal Recessive Cerebellar Ataxias in South America: A Multicenter Study of 1338 Patients. Mov Disord 2022. [PMID: 35507441 DOI: 10.1002/mds.29046] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
40 Manto M, Gandini J, Feil K, Strupp M. Cerebellar ataxias: an update. Current Opinion in Neurology 2020;33:150-60. [DOI: 10.1097/wco.0000000000000774] [Cited by in Crossref: 18] [Cited by in F6Publishing: 12] [Article Influence: 9.0] [Reference Citation Analysis]
41 Subramony S, Burns M, Kugelmann EL, Zingariello CD. Inherited Ataxias In Children. Pediatric Neurology 2022. [DOI: 10.1016/j.pediatrneurol.2022.04.004] [Reference Citation Analysis]
42 Lieto M, Riso V, Galatolo D, De Michele G, Rossi S, Barghigiani M, Cocozza S, Pontillo G, Trovato R, Saccà F, Salvatore E, Tessa A, Filla A, Santorelli FM, De Michele G, Silvestri G. The complex phenotype of spinocerebellar ataxia type 48 in eight unrelated Italian families. Eur J Neurol 2020;27:498-505. [PMID: 31571321 DOI: 10.1111/ene.14094] [Cited by in Crossref: 26] [Cited by in F6Publishing: 20] [Article Influence: 8.7] [Reference Citation Analysis]
43 Teive HA, Iliadou VM, Manto M. Friedreich's Ataxia and Auditory Processing Disorder. Cerebellum 2021;20:495-6. [PMID: 33599953 DOI: 10.1007/s12311-021-01238-7] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
44 Indelicato E, Fanciulli A, Nachbauer W, Eigentler A, Amprosi M, Ndayisaba JP, Granata R, Wenning G, Boesch S. Cardiovascular autonomic testing in the work-up of cerebellar ataxia: insight from an observational single center study. J Neurol 2020;267:1097-102. [PMID: 31893293 DOI: 10.1007/s00415-019-09684-4] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
45 Brankovic M, Dragasevic N, Dobricic V, Maver A, Bergant G, Petrovic I, Peric S, Marjanovic A, Jankovic M, Jancic J, Novakovic I, Peterlin B, Svetel M, Kostic V. Clinical exome sequencing in Serbian patients with movement disorders: Single centre experience. Genetika 2022;54:395-409. [DOI: 10.2298/gensr2201395b] [Reference Citation Analysis]