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Journal Abstract Search

3412 related items for PubMed ID: 19487653

  • 1. Clinical features that distinguish PLS, upper motor neuron-dominant ALS, and typical ALS.
    Gordon PH, Cheng B, Katz IB, Mitsumoto H, Rowland LP.
    Neurology; 2009 Jun 02; 72(22):1948-52. PubMed ID: 19487653
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  • 2. The natural history of primary lateral sclerosis.
    Gordon PH, Cheng B, Katz IB, Pinto M, Hays AP, Mitsumoto H, Rowland LP.
    Neurology; 2006 Mar 14; 66(5):647-53. PubMed ID: 16534101
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  • 3. A long-term prospective study of the natural course of sporadic adult-onset lower motor neuron syndromes.
    Van den Berg-Vos RM, Visser J, Kalmijn S, Fischer K, de Visser M, de Jong V, de Haan RJ, Franssen H, Wokke JH, Van den Berg LH.
    Arch Neurol; 2009 Jun 14; 66(6):751-7. PubMed ID: 19506135
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  • 8. Quantitative objective markers for upper and lower motor neuron dysfunction in ALS.
    Mitsumoto H, Ulug AM, Pullman SL, Gooch CL, Chan S, Tang MX, Mao X, Hays AP, Floyd AG, Battista V, Montes J, Hayes S, Dashnaw S, Kaufmann P, Gordon PH, Hirsch J, Levin B, Rowland LP, Shungu DC.
    Neurology; 2007 Apr 24; 68(17):1402-10. PubMed ID: 17452585
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  • 10. Onset and spreading patterns of upper and lower motor neuron symptoms in amyotrophic lateral sclerosis.
    Körner S, Kollewe K, Fahlbusch M, Zapf A, Dengler R, Krampfl K, Petri S.
    Muscle Nerve; 2011 May 24; 43(5):636-42. PubMed ID: 21484822
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  • 11. [Objective markers for upper motor neuron involvement in amyotrophic lateral sclerosis].
    Iwata NK.
    Brain Nerve; 2007 Oct 24; 59(10):1053-64. PubMed ID: 17969345
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  • 13. [Differential diagnosis and atypical subsets of amyotrophic lateral sclerosis].
    Pradat PF, Bruneteau G.
    Rev Neurol (Paris); 2006 Jun 24; 162 Spec No 2():4S81-4S90. PubMed ID: 17128093
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  • 14. Natural history of young-adult amyotrophic lateral sclerosis.
    Sabatelli M, Madia F, Conte A, Luigetti M, Zollino M, Mancuso I, Lo Monaco M, Lippi G, Tonali P.
    Neurology; 2008 Sep 16; 71(12):876-81. PubMed ID: 18596241
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  • 15. Uncovering amyotrophic lateral sclerosis phenotypes: clinical features and long-term follow-up of upper motor neuron-dominant ALS.
    Sabatelli M, Zollino M, Luigetti M, Grande AD, Lattante S, Marangi G, Monaco ML, Madia F, Meleo E, Bisogni G, Conte A.
    Amyotroph Lateral Scler; 2011 Jul 16; 12(4):278-82. PubMed ID: 21702734
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  • 16. Transcallosal inhibition in amyotrophic lateral sclerosis.
    Wittstock M, Wolters A, Benecke R.
    Clin Neurophysiol; 2007 Feb 16; 118(2):301-7. PubMed ID: 17140846
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  • 19. Motor unit firing in amyotrophic lateral sclerosis and other upper and lower motor neurone disorders.
    de Carvalho M, Turkman A, Swash M.
    Clin Neurophysiol; 2012 Nov 16; 123(11):2312-8. PubMed ID: 22627021
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  • 20. Hemiplegic ALS: Mills syndrome.
    Rajabally YA, Hbahbih M, Abbott RJ.
    Neurology; 2005 Jun 14; 64(11):1984-5. PubMed ID: 15955966
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