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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

162 related items for PubMed ID: 5730656

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  • 3. [Sectorial pigmented retinopathy secondary to acquired syphilis].
    Cristiani R.
    Ann Ottalmol Clin Ocul; 1967 Oct; 93(10):1099-108. PubMed ID: 5605815
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  • 7. Genetic approach to the nosology of retinal disorders.
    Klein D.
    Birth Defects Orig Artic Ser; 1971 Mar; 7(3):52-82. PubMed ID: 4950917
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  • 11. Opsoclonus--myoclonus in acute cerebellar ataxia.
    Mitra A, Bajaj S.
    J Assoc Physicians India; 1987 Dec; 35(12):853-5. PubMed ID: 3449544
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  • 12. [Myoclonic cerebellar dyssynergy (Ramsay Hunt syndrome)].
    Roger J, Soulayrol R, Hassoun J.
    Rev Neurol (Paris); 1968 Jul; 119(1):85-106. PubMed ID: 5720761
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  • 13. [Tapetoretinal degeneration and heredo-ataxia (apropos of a family)].
    Bigorgne J, Halot-Boyer P, Hermann P.
    Bull Soc Ophtalmol Fr; 1971 Mar; 71(3):361-4. PubMed ID: 5139468
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  • 15. Leber's congenital tapetoretinal degeneration.
    Francois J.
    Int Ophthalmol Clin; 1968 Mar; 8(4):929-47. PubMed ID: 5741529
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  • 17. [A case of juvenile onset ataxia with dystonia, myoclonus, sensorineural hearing loss and mental retardation].
    Koide R, Yoshimura N, Soma Y, Tsuji S.
    Rinsho Shinkeigaku; 1993 Aug; 33(8):909-11. PubMed ID: 8261707
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  • 19. [A case of congenital non-progressive cerebellar ataxia with pigmentary retinal degeneration, fiber type disproportion and hypercreatine kinasemia].
    Yamasaki T, Taniwaki T, Kikuchi H, Araki E, Arakawa K, Iwaki T, Yamada T, Kira J.
    Rinsho Shinkeigaku; 1999 Sep; 39(9):925-9. PubMed ID: 10614155
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