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Journal Abstract Search

159 related items for PubMed ID: 1646519

  • 1. [The preclinical DNA diagnosis of Huntington's chorea].
    Badalian LO, Evgrafov OV, Groppa SA, Proskurina LA, Malygina NA, Makarov VB.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1991; 91(3):103-5. PubMed ID: 1646519
    [Abstract] [Full Text] [Related]

  • 2. [Presymptomatic diagnosis in Huntington chorea families using the gene amplification technique].
    Lucotte G, Berriche S, Petit MC, Burckel A, Turpin JC.
    Rev Neurol (Paris); 1991; 147(8-9):602-4. PubMed ID: 1835796
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  • 3. [Molecular diagnosis of Huntington's disease: an analysis of two large families].
    Zeng Y, Chen M, Mao Y.
    Zhonghua Yi Xue Za Zhi; 1995 Nov; 75(11):689-93, 711-2. PubMed ID: 8697093
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  • 4. Molecular diagnosis of Huntington's disease in Mexican patients by polymerase chain reaction.
    Cisneros Vega B, Alonso Vilatela ME, Yescas Gomez P, Silva Arreola G, Montañez Ojeda C.
    Arch Med Res; 1996 Nov; 27(1):87-92. PubMed ID: 8867374
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  • 6. [Use of polymorphous DNA probes in the study of French families with Huntington's chorea].
    Lucotte G, Berriche S, Burckel A, Turpin JC.
    Rev Neurol (Paris); 1990 Nov; 146(4):303-5. PubMed ID: 1972803
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  • 9. [Genetic counseling on a molecular basis for Huntington's chorea].
    Cassiman JJ.
    J Genet Hum; 1989 Jan; 37(1):13-24. PubMed ID: 2565951
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  • 10. [Huntington's chorea: clinical aspects, genetics and current diagnosis].
    Spiegel R.
    Ther Umsch; 1995 Dec; 52(12):814-20. PubMed ID: 8539653
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  • 12. [Huntington chorea: (CAG)n repeats on gene IT 15 in Austria].
    Meszaros K, Willinger U, Heiden AM, Fuchs K, Baumhackl U, Brücke T, Feucht M, Fathi N, Lenzinger E, Miller E.
    Wien Klin Wochenschr; 1994 Dec; 106(21):671-2. PubMed ID: 7810152
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  • 14. Genetic prediction in Huntington's disease: what are the limitations imposed by pedigree structure?
    Misra VP, Baraitser M, Harding AE.
    Mov Disord; 1988 Dec; 3(3):233-6. PubMed ID: 2973561
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  • 15. [The characteristics of the familial polymorphism of Huntington's chorea].
    Groppa SA, Tagiev ESh.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1991 Dec; 91(11):59-64. PubMed ID: 1666228
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  • 16. [Gene identification for Huntington's disease. Direkt mutational analysis confirms the diagnosis].
    Almqvist E, Björck E, Wahlström J, Nylander PO, Holmgren G, Kristoffersson U, Anvret M.
    Lakartidningen; 1995 Jan 04; 92(1-2):28-31. PubMed ID: 7830456
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  • 17. [Organic dementia as a first symptom of infantile Huntington's chorea (author's transl)].
    Maida E, Schnaberth G.
    Wien Klin Wochenschr; 1976 Dec 10; 88(23):775-7. PubMed ID: 138265
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  • 18. Cortical myoclonus in Huntington's disease.
    Thompson PD, Bhatia KP, Brown P, Davis MB, Pires M, Quinn NP, Luthert P, Honovar M, O'Brien MD, Marsden CD.
    Mov Disord; 1994 Nov 10; 9(6):633-41. PubMed ID: 7845404
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  • 19. [DNA markers linked to Huntington's disease (D4S10 and D4S95) in Spanish families: preliminary results].
    Benítez J, Ramos C, Fernández E, Ayuso C, Yébenes J.
    Rev Clin Esp; 1992 Apr 10; 190(6):299-301. PubMed ID: 1350862
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  • 20. A case of Huntington's chorea in a Nigerian and the sociocultural factors associated with its diagnosis and management.
    Morakinyo O.
    Trop Geogr Med; 1983 Mar 10; 35(1):69-72. PubMed ID: 6225232
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