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Journal Abstract Search

191 related items for PubMed ID: 6884951

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  • 4. [Bite anomalies in familial Friedreich's ataxia].
    Gorin NN, Gurskaia NZ.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1978; 78(11):1625-7. PubMed ID: 726755
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  • 6. Friedreich's Ataxia 1978--an overview.
    Barbeau A.
    Can J Neurol Sci; 1978 Feb; 5(1):161-5. PubMed ID: 647493
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  • 7. [Bite anomalies in familial Friedreich's ataxia].
    Gurskaia NZ, Gorin NN.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1978 Feb; 78(3):255-7. PubMed ID: 645307
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  • 8. [Acute myocardial infarct and Friedreich's disease].
    Calvo Iglesias FE, Permanyer Miralda G, Blanco Castiñeiras J, Rodés Cabau J, Anivarro Blanco I, Soler Soler J.
    Rev Esp Cardiol; 1995 Feb; 48(2):145-7. PubMed ID: 7886266
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  • 11. [Cardiac manifestations of Friedreich's ataxia].
    Kolek M, Mrózek V, Schenk P.
    Cas Lek Cesk; 2004 Feb; 143(1):48-51. PubMed ID: 15061120
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  • 12. [Morphological changes in familial ataxia (Friedreich's disease)].
    Vavilova TI.
    Arkh Patol; 1980 Feb; 42(2):71-3. PubMed ID: 7362478
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  • 13. [Contribution to the nosographic definition of forms intermediate between Friedreich's disease and Charcot-Marie-Tooth amyotrophy].
    SANGUINETI I.
    Riv Sper Freniatr Med Leg Alien Ment; 1953 Dec 31; 77(4):513-46. PubMed ID: 13168196
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  • 14. Hypertrophic cardiomyopathy in Friedreich's ataxia.
    Fayssoil A, Nardi O, Orlikowski D, Annane D.
    Int J Cardiol; 2008 Jul 21; 127(3):e122-3. PubMed ID: 17659792
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  • 15. [Are Friedreich's disease, Charcot-Marie disease and Déjérine-Sottas disease distinct nosologic entities? Two familial cases with associated syndromes].
    BULGARELLI R, LEVA R.
    Minerva Pediatr; 1954 Jul 15; 6(13):497-502. PubMed ID: 13203336
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  • 17. A syndrome resembling Friedreich's ataxia with relapsing polyneuropathy and hyperalaninemia.
    Dunn HG, Perry TL, Dolman CL.
    Neurology; 1968 Mar 15; 18(3):301. PubMed ID: 5690400
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  • 18. Identification and sizing of GAA trinucleotide repeat expansion, investigation for D-loop variations and mitochondrial deletions in Iranian patients with Friedreich's ataxia.
    Houshmand M, Panahi MS, Nafisi S, Soltanzadeh A, Alkandari FM.
    Mitochondrion; 2006 Apr 15; 6(2):82-8. PubMed ID: 16581313
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  • 19. Friedreich's ataxia mimicking hereditary motor and sensory neuropathy.
    Panas M, Kalfakis N, Karadima G, Davaki P, Vassilopoulos D.
    J Neurol; 2002 Nov 15; 249(11):1583-6. PubMed ID: 12420100
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