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Journal Abstract Search

740 related items for PubMed ID: 17620549

  • 21. MRI-based volumetric differentiation of sporadic cerebellar ataxia.
    Burk K, Globas C, Wahl T, Bühring U, Dietz K, Zuhlke C, Luft A, Schulz JB, Voigt K, Dichgans J.
    Brain; 2004 Jan; 127(Pt 1):175-81. PubMed ID: 14570820
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  • 22. TUBB4A de novo mutations cause isolated hypomyelination.
    Pizzino A, Pierson TM, Guo Y, Helman G, Fortini S, Guerrero K, Saitta S, Murphy JL, Padiath Q, Xie Y, Hakonarson H, Xu X, Funari T, Fox M, Taft RJ, van der Knaap MS, Bernard G, Schiffmann R, Simons C, Vanderver A.
    Neurology; 2014 Sep 02; 83(10):898-902. PubMed ID: 25085639
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  • 23. Dominant olivopontocerebellar atrophy with dementia and extrapyramidal signs: report of a family through three generations.
    Konigsmark BW, Lipton HL.
    Birth Defects Orig Artic Ser; 1971 Feb 02; 7(1):178-91. PubMed ID: 5173358
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  • 24. Early-onset neurodegenerative disease of the cerebellum and motor axons.
    Salman MS, Marles SL, Booth FA, Del Bigio MR.
    Pediatr Neurol; 2009 May 02; 40(5):365-70. PubMed ID: 19380073
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  • 25. New syndrome characterized by hypomyelination with atrophy of the basal ganglia and cerebellum.
    van der Knaap MS, Naidu S, Pouwels PJ, Bonavita S, van Coster R, Lagae L, Sperner J, Surtees R, Schiffmann R, Valk J.
    AJNR Am J Neuroradiol; 2002 Oct 02; 23(9):1466-74. PubMed ID: 12372733
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  • 26. Novel TUBB4A mutations and expansion of the neuroimaging phenotype of hypomyelination with atrophy of the basal ganglia and cerebellum (H-ABC).
    Ferreira C, Poretti A, Cohen J, Hamosh A, Naidu S.
    Am J Med Genet A; 2014 Jul 02; 164A(7):1802-7. PubMed ID: 24706558
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  • 27. Hemolytic-uremic syndrome with involvement of basal ganglia and cerebellum.
    Hager A, Staudt M, Klare B, von Einsiedel HG, Krägeloh-Mann I.
    Neuropediatrics; 1999 Aug 02; 30(4):210-3. PubMed ID: 10569213
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  • 29. Central nervous system involvement in hereditary neuropathy with liability to pressure palsies: description of a large family with this association.
    Sanahuja J, Franco E, Rojas-García R, Gallardo E, Combarros O, Begué R, Granés P, Illa I.
    Arch Neurol; 2005 Dec 02; 62(12):1911-4. PubMed ID: 16344349
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  • 33. Severe TUBB4A-Related Hypomyelination With Atrophy of the Basal Ganglia and Cerebellum: Novel Neuropathological Findings.
    Joyal KM, Michaud J, van der Knaap MS, Bugiani M, Venkateswaran S.
    J Neuropathol Exp Neurol; 2019 Jan 01; 78(1):3-9. PubMed ID: 30476126
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  • 34. The spectrum of mutations for the diagnosis of vanishing white matter disease.
    Scali O, Di Perri C, Federico A.
    Neurol Sci; 2006 Sep 01; 27(4):271-7. PubMed ID: 16998732
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  • 35. Distribution of cerebello-olivary degeneration in idiopathic late cortical cerebellar atrophy: clinicopathological study of four autopsy cases.
    Ota S, Tsuchiya K, Anno M, Niizato K, Akiyama H.
    Neuropathology; 2008 Feb 01; 28(1):43-50. PubMed ID: 18181834
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  • 40. Recognizable inherited syndrome of progressive central nervous system degeneration and generalized intracranial calcification with overlapping phenotype of the syndrome of Aicardi and Goutières.
    Kumar D, Rittey C, Cameron AH, Variend S.
    Am J Med Genet; 1998 Feb 17; 75(5):508-15. PubMed ID: 9489795
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