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Journal Abstract Search

226 related items for PubMed ID: 7557682

  • 1.
    ; . PubMed ID:
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  • 2. Prevalence of glucocerebrosidase mutations in the Israeli Ashkenazi Jewish population.
    Horowitz M, Pasmanik-Chor M, Borochowitz Z, Falik-Zaccai T, Heldmann K, Carmi R, Parvari R, Beit-Or H, Goldman B, Peleg L, Levy-Lahad E, Renbaum P, Legum S, Shomrat R, Yeger H, Benbenisti D, Navon R, Dror V, Shohat M, Magal N, Navot N, Eyal N.
    Hum Mutat; 1998; 12(4):240-4. PubMed ID: 9744474
    [Abstract] [Full Text] [Related]

  • 3. Lower frequency of Gaucher disease carriers among Tay-Sachs disease carriers.
    Peleg L, Frisch A, Goldman B, Karpaty M, Narinsky R, Bronstein S, Frydman M.
    Eur J Hum Genet; 1998; 6(2):185-6. PubMed ID: 9781065
    [Abstract] [Full Text] [Related]

  • 4. Linkage to Gaucher mutations in the Ashkenazi population: effect of drift on decay of linkage disequilibrium and evidence for heterozygote selection.
    Boas FE.
    Blood Cells Mol Dis; 2000 Aug; 26(4):348-59. PubMed ID: 11042036
    [Abstract] [Full Text] [Related]

  • 5. Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews.
    Aharon-Peretz J, Rosenbaum H, Gershoni-Baruch R.
    N Engl J Med; 2004 Nov 04; 351(19):1972-7. PubMed ID: 15525722
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  • 7. Population study of chronic Gaucher's disease.
    Fried K.
    Isr J Med Sci; 1973 Nov 04; 9(9):1396-8. PubMed ID: 4775122
    [No Abstract] [Full Text] [Related]

  • 8. The 1226G (N370S) Gaucher mutation among patients with Legg-Calve-Perthes disease.
    Kenet G, Hayek S, Mor M, Lubetsky A, Miller L, Rosenberg N, Mosheiff R, Itzchaki M, Elstein D, Wientroub S, Zimran A.
    Blood Cells Mol Dis; 2003 Nov 04; 31(1):72-4. PubMed ID: 12850487
    [Abstract] [Full Text] [Related]

  • 9. New insights into the origin of the Gaucher disease-causing mutation N370S: extended haplotype analysis using the 5GC3.2, 5470 G/A, and ITG6.2 polymorphisms.
    Rodríguez-Marí A, Díaz-Font A, Chabás A, Pastores GM, Grinberg D, Vilageliu L.
    Blood Cells Mol Dis; 2001 Nov 04; 27(5):950-9. PubMed ID: 11783960
    [Abstract] [Full Text] [Related]

  • 10. [Jewish identity and immigration to Israel: an ongoing survey among the current wave of Russian immigrants].
    Damian N, Rosenbaum-tamari Y.
    Rev Eur Migr Int; 1996 Nov 04; 12(3):123-38. PubMed ID: 12292939
    [Abstract] [Full Text] [Related]

  • 11. Linkage disequilibrium of common Gaucher disease mutations with a polymorphic site in the pyruvate kinase (PKLR) gene.
    Rockah R, Narinsky R, Frydman M, Cohen IJ, Zaizov R, Weizman A, Frisch A.
    Am J Med Genet; 1998 Jul 07; 78(3):233-6. PubMed ID: 9677056
    [Abstract] [Full Text] [Related]

  • 12. Perthes' disease and the search for genetic associations: collagen mutations, Gaucher's disease and thrombophilia.
    Kenet G, Ezra E, Wientroub S, Steinberg DM, Rosenberg N, Waldman D, Hayek S.
    J Bone Joint Surg Br; 2008 Nov 07; 90(11):1507-11. PubMed ID: 18978274
    [Abstract] [Full Text] [Related]

  • 13. High frequency of the Gaucher disease mutation at nucleotide 1226 among Ashkenazi Jews.
    Zimran A, Gelbart T, Westwood B, Grabowski GA, Beutler E.
    Am J Hum Genet; 1991 Oct 07; 49(4):855-9. PubMed ID: 1897529
    [Abstract] [Full Text] [Related]

  • 14. The selective advantage of Gaucher's disease: TB or not TB?
    Kannai R, Elstein D, Weiler-Razell D, Zimran A.
    Isr J Med Sci; 1994 Dec 07; 30(12):911-2. PubMed ID: 8002277
    [No Abstract] [Full Text] [Related]

  • 15. Frequency of carriers of chronic (type I) Gaucher disease in Ashkenazi Jews.
    Matoth Y, Chazan S, Cnaan A, Gelernter I, Klibansky C.
    Am J Med Genet; 1987 Jul 07; 27(3):561-5. PubMed ID: 3631130
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  • 18. Gaucher disease: gene frequencies in the Ashkenazi Jewish population.
    Beutler E, Nguyen NJ, Henneberger MW, Smolec JM, McPherson RA, West C, Gelbart T.
    Am J Hum Genet; 1993 Jan 07; 52(1):85-8. PubMed ID: 8434610
    [Abstract] [Full Text] [Related]

  • 19. NOD2/CARD15 genotype and phenotype differences between Ashkenazi and Sephardic Jews with Crohn's disease.
    Karban A, Waterman M, Panhuysen CI, Pollak RD, Nesher S, Datta L, Weiss B, Suissa A, Shamir R, Brant SR, Eliakim R.
    Am J Gastroenterol; 2004 Jun 07; 99(6):1134-40. PubMed ID: 15180737
    [Abstract] [Full Text] [Related]

  • 20. Type 2 Gaucher disease with hydrops fetalis in an Ashkenazi Jewish family resulting from a novel recombinant allele and a rare splice junction mutation in the glucocerebrosidase locus.
    Reissner K, Tayebi N, Stubblefield BK, Koprivica V, Blitzer M, Holleran W, Cowan T, Almashanu S, Maddalena A, Karson EM, Sidransky E.
    Mol Genet Metab; 1998 Apr 07; 63(4):281-8. PubMed ID: 9635296
    [Abstract] [Full Text] [Related]

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