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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

372 related items for PubMed ID: 17574095

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  • 6. Racing against the clock: recognizing, differentiating, diagnosing, and referring the amyotrophic lateral sclerosis patient.
    Shook SJ, Pioro EP.
    Ann Neurol; 2009 Jan; 65 Suppl 1():S10-6. PubMed ID: 19191305
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  • 8. Molecular basis of treatment in motor neurone disease.
    Anneser J.
    Neurol Sci; 2000 Jan; 21(5 Suppl):S913-8. PubMed ID: 11382189
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  • 12. [Amyotrophic lateral sclerosis: management of bulbar symptoms].
    Kraft P, Beck M, Grimm A, Wessig C, Reiners K, Toyka KV.
    Nervenarzt; 2010 Oct; 81(10):1218-25. PubMed ID: 20401600
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  • 13. Proposed criteria for familial amyotrophic lateral sclerosis.
    Byrne S, Bede P, Elamin M, Kenna K, Lynch C, McLaughlin R, Hardiman O.
    Amyotroph Lateral Scler; 2011 May; 12(3):157-9. PubMed ID: 21208036
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  • 15. Managing amyotrophic lateral sclerosis: slowing disease progression and improving patient quality of life.
    Brooks BR.
    Ann Neurol; 2009 Jan; 65 Suppl 1():S17-23. PubMed ID: 19191306
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  • 16. Protein disulphide isomerase protects against protein aggregation and is S-nitrosylated in amyotrophic lateral sclerosis.
    Walker AK, Farg MA, Bye CR, McLean CA, Horne MK, Atkin JD.
    Brain; 2010 Jan; 133(Pt 1):105-16. PubMed ID: 19903735
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  • 18. Recent advances in the therapy of amyotrophic lateral sclerosis: focus on excitotoxicity.
    Brighina L, Sala G, Ceresa C, Tremolizzo L, Ferrarese C.
    Funct Neurol; 2001 Jan; 16(4 Suppl):189-202. PubMed ID: 11996516
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  • 20. Molecular biology of amyotrophic lateral sclerosis: insights from genetics.
    Pasinelli P, Brown RH.
    Nat Rev Neurosci; 2006 Sep; 7(9):710-23. PubMed ID: 16924260
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