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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

98 related items for PubMed ID: 492674

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  • 5. [Clinical and genetic analysis of 188 families with spinocerebellar degeneration. Friedreich's disease and P. Marie's hereditary ataxias].
    Ben Hamida M, Attia-Romdhane N, Triki CH, Oueslati S, Hentati F.
    Rev Neurol (Paris); 1991; 147(12):798-808. PubMed ID: 1780608
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  • 9. [Congestive cardiomyopathy and pyruvate elevation in a case of Charcot-Marie-Tooth disease].
    Martin-Du Pan RC, Juge C, Perrenoud JJ.
    Schweiz Med Wochenschr; 1984 May 05; 114(18):625-9. PubMed ID: 6539500
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  • 14. [Heredoataxia and tapetoretinal degeneration (genetic relation)].
    Boyazis RM, Hariga J, Myle G.
    Encephale; 1968 May 05; 57(6):495-514. PubMed ID: 5730656
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  • 17. Infantile motor neuron diseases.
    Pearn JH.
    Adv Neurol; 1982 May 05; 36():121-30. PubMed ID: 7180678
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  • 18. [Electroencephalographic changes in Firedreich's and Pierre-Marie disease].
    Salaeva ZM, Gasanov IaK, Magalov ShI.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1975 May 05; 75(6):836-9. PubMed ID: 1217384
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  • 19. [Role of electroretinography in the prognosis of central retinal vein occlusion].
    Dujić M, Nikolić Lj.
    Srp Arh Celok Lek; 1997 May 05; 125(7-8):214-8. PubMed ID: 9304234
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