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Pubmed for Handhelds

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Journal Abstract Search

191 related items for PubMed ID: 21208036

  • 61.
    ; . PubMed ID:
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  • 62. Criteria for diagnosis of familial amyotrophic lateral sclerosis. European FALS Collaborative Group.
    Swash M, Leigh N.
    Neuromuscul Disord; 1992; 2(1):7-9. PubMed ID: 1356048
    [Abstract] [Full Text] [Related]

  • 63. An update on superoxide dismutase 1 in familial amyotrophic lateral sclerosis.
    Cudkowicz ME, Brown RH.
    J Neurol Sci; 1996 Aug; 139 Suppl():10-5. PubMed ID: 8899652
    [No Abstract] [Full Text] [Related]

  • 64.
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  • 65. A specific superoxide dismutase mutation is on the same genetic background in sporadic and familial cases of amyotrophic lateral sclerosis.
    Hayward C, Swingler RJ, Simpson SA, Brock DJ.
    Am J Hum Genet; 1996 Nov; 59(5):1165-7. PubMed ID: 8900247
    [No Abstract] [Full Text] [Related]

  • 66. A natural history comparison of SOD1-mutant patients with amyotrophic lateral sclerosis between Chinese and German populations.
    Tang L, Dorst J, Chen L, Liu X, Ma Y, Günther K, Michels S, Müller K, Freischmidt A, Weishaupt JH, Fan D, Ludolph AC.
    Transl Neurodegener; 2021 Oct 28; 10(1):42. PubMed ID: 34711284
    [No Abstract] [Full Text] [Related]

  • 67.
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  • 68.
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  • 69. Susceptibility genes in sporadic ALS: separating the wheat from the chaff by international collaboration.
    Shaw CE, Al-Chalabi A.
    Neurology; 2006 Sep 12; 67(5):738-9. PubMed ID: 16966531
    [No Abstract] [Full Text] [Related]

  • 70. Microhemorrhages: undetectable but clinically meaningful the question persists.
    Zhong Z, Winkler EA, Zlokovic BV.
    Amyotroph Lateral Scler; 2011 May 12; 12(3):231-2; author reply 233-4. PubMed ID: 21413850
    [No Abstract] [Full Text] [Related]

  • 71.
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  • 72. Superoxide dismutase in familial amyotrophic lateral sclerosis: models for gain of function.
    Brown RH.
    Curr Opin Neurobiol; 1995 Dec 12; 5(6):841-6. PubMed ID: 8805422
    [No Abstract] [Full Text] [Related]

  • 73. The expanding syndrome of amyotrophic lateral sclerosis: a clinical and molecular odyssey.
    Turner MR, Swash M.
    J Neurol Neurosurg Psychiatry; 2015 Jun 12; 86(6):667-73. PubMed ID: 25644224
    [Abstract] [Full Text] [Related]

  • 74. [Motor neuron disease specific subtypes in isolated bulbar phenotype of amyotrophic lateral sclerosis].
    Huang X, Fan DS.
    Zhonghua Nei Ke Za Zhi; 2017 Mar 01; 56(3):229-230. PubMed ID: 28253610
    [No Abstract] [Full Text] [Related]

  • 75.
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  • 76.
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  • 77. Machine learning: Calculating disease.
    Savage N.
    Nature; 2017 Oct 18; 550(7676):S115-S117. PubMed ID: 29045372
    [No Abstract] [Full Text] [Related]

  • 78.
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  • 79. Major advances in amyotrophic lateral sclerosis in 2020.
    Hardiman O.
    Lancet Neurol; 2021 Jan 18; 20(1):14-15. PubMed ID: 33340474
    [No Abstract] [Full Text] [Related]

  • 80. Atypical forms of familial amyotrophic lateral sclerosis.
    Gregoire N, Serratrice G.
    Adv Exp Med Biol; 1987 Jan 18; 209():159-64. PubMed ID: 3577907
    [No Abstract] [Full Text] [Related]

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