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Journal Abstract Search

174 related items for PubMed ID: 38880819

  • 1. An MRI evaluation of white matter involvement in paradigmatic forms of spastic ataxia: results from the multi-center PROSPAX study.
    Scaravilli A, Gabusi I, Mari G, Battocchio M, Bosticardo S, Schiavi S, Bender B, Kessler C, Brais B, La Piana R, van de Warrenburg BP, Cosottini M, Timmann D, PROSPAX Consortium, Daducci A, Schüle R, Synofzik M, Santorelli FM, Cocozza S.
    J Neurol; 2024 Aug; 271(8):5468-5477. PubMed ID: 38880819
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  • 2. MRI-ARSACS: An Imaging Index for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) Identification Based on the Multicenter PROSPAX Study.
    Scaravilli A, Negroni D, Senatore C, Ugga L, Cosottini M, Ricca I, Bender B, Traschütz A, Başak AN, Vural A, van de Warrenburg BP, Durr A, La Piana R, Timmann D, PROSPAX Consortium, Schüle R, Synofzik M, Santorelli FM, Cocozza S.
    Mov Disord; 2024 Aug; 39(8):1343-1351. PubMed ID: 38847051
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  • 3. Spastic ataxias.
    Bereznyakova O, Dupré N.
    Handb Clin Neurol; 2018 Aug; 155():191-203. PubMed ID: 29891058
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  • 4. Assessment of whole-brain white matter by DTI in autosomal recessive spastic ataxia of Charlevoix-Saguenay.
    Oguz KK, Haliloglu G, Temucin C, Gocmen R, Has AC, Doerschner K, Dolgun A, Alikasifoglu M.
    AJNR Am J Neuroradiol; 2013 Oct; 34(10):1952-7. PubMed ID: 23598833
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  • 5. Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS) in a Thai Patient: The Classic Clinical Manifestations, Funduscopic Feature, and Brain Imaging Findings with a Novel Mutation in the SACS Gene.
    Srikajon J, Pitakpatapee Y, Limwongse C, Chirapapaisan N, Srivanitchapoom P.
    Tremor Other Hyperkinet Mov (N Y); 2020 Jun 08; 10():1. PubMed ID: 32775015
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  • 6. Retinal Architecture in Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS): Insights into Disease Pathogenesis and Biomarkers.
    Rezende Filho FM, Bremner F, Pedroso JL, de Andrade JBC, Marianelli BF, Lourenço CM, Marques-Júnior W, França MC, Kok F, Sallum JMF, Parkinson MH, Barsottini OG, Giunti P.
    Mov Disord; 2021 Sep 08; 36(9):2027-2035. PubMed ID: 33893680
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  • 7. Neurophysiological and ophthalmological findings of SPG7-related spastic ataxia: a phenotype study in an Irish cohort.
    Bogdanova-Mihaylova P, Chen H, Plapp HM, Gorman C, Alexander MD, McHugh JC, Moran S, Early A, Cassidy L, Lynch T, Murphy SM, Walsh RA.
    J Neurol; 2021 Oct 08; 268(10):3897-3907. PubMed ID: 33774748
    [Abstract] [Full Text] [Related]

  • 8. Abnormal Paraplegin Expression in Swollen Neurites, τ- and α-Synuclein Pathology in a Case of Hereditary Spastic Paraplegia SPG7 with an Ala510Val Mutation.
    Thal DR, Züchner S, Gierer S, Schulte C, Schöls L, Schüle R, Synofzik M.
    Int J Mol Sci; 2015 Oct 21; 16(10):25050-66. PubMed ID: 26506339
    [Abstract] [Full Text] [Related]

  • 9. Clinical and Molecular Findings of Autosomal Recessive Spastic Ataxia of Charlevoix Saguenay: an Iranian Case Series Expanding the Genetic and Neuroimaging Spectra.
    Ashrafi MR, Mohammadi P, Tavasoli AR, Heidari M, Hosseinpour S, Rasulinejad M, Rohani M, Akbari MG, Malamiri RA, Badv RS, Fathi D, Dehnavi AZ, Savad S, Rabbani A, Synofzik M, Mahdieh N, Rezaei Z.
    Cerebellum; 2023 Aug 21; 22(4):640-650. PubMed ID: 35731353
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  • 11. Hypomorphic mutations in POLR3A are a frequent cause of sporadic and recessive spastic ataxia.
    Minnerop M, Kurzwelly D, Wagner H, Soehn AS, Reichbauer J, Tao F, Rattay TW, Peitz M, Rehbach K, Giorgetti A, Pyle A, Thiele H, Altmüller J, Timmann D, Karaca I, Lennarz M, Baets J, Hengel H, Synofzik M, Atasu B, Feely S, Kennerson M, Stendel C, Lindig T, Gonzalez MA, Stirnberg R, Sturm M, Roeske S, Jung J, Bauer P, Lohmann E, Herms S, Heilmann-Heimbach S, Nicholson G, Mahanjah M, Sharkia R, Carloni P, Brüstle O, Klopstock T, Mathews KD, Shy ME, de Jonghe P, Chinnery PF, Horvath R, Kohlhase J, Schmitt I, Wolf M, Greschus S, Amunts K, Maier W, Schöls L, Nürnberg P, Zuchner S, Klockgether T, Ramirez A, Schüle R.
    Brain; 2017 Jun 01; 140(6):1561-1578. PubMed ID: 28459997
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  • 15. Brain white matter involvement in hereditary spastic paraplegias: analysis with multiple diffusion tensor indices.
    Aghakhanyan G, Martinuzzi A, Frijia F, Vavla M, Hlavata H, Baratto A, Martino N, Paparella G, Montanaro D.
    AJNR Am J Neuroradiol; 2014 Aug 01; 35(8):1533-8. PubMed ID: 24788132
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  • 16. Widening the clinical, radiological and genetic spectrum of autosomal recessive ataxia of Charlevoix-Saguenay in Indian patients.
    Divya KP, Cherian A, Dhing HK, Kumar S, Thomas B, Faruq M.
    Acta Neurol Belg; 2024 Apr 01; 124(2):475-484. PubMed ID: 37898963
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  • 17. Relationship between brain white matter damage and grey matter atrophy in hereditary spastic paraplegia types 4 and 5.
    Tu Y, Liu Y, Fan S, Weng J, Li M, Zhang F, Fu Y, Hu J.
    Eur J Neurol; 2024 Aug 01; 31(8):e16310. PubMed ID: 38651515
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  • 18. Spinal Cord Gray and White Matter Damage in Different Hereditary Spastic Paraplegia Subtypes.
    Servelhere KR, Casseb RF, de Lima FD, Rezende TJR, Ramalho LP, França MC.
    AJNR Am J Neuroradiol; 2021 Mar 01; 42(3):610-615. PubMed ID: 33478946
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