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Journal Abstract Search

127 related items for PubMed ID: 6766519

  • 1.
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  • 2. Morquio-like syndrome with beta galactosidase deficiency and normal hexosamine sulfatase activity: mucopolysacchariodosis IVB.
    Arbisser AI, Donnelly KA, Scott CI, DiFerrante N, Singh J, Stevenson RE, Aylesworth AS, Howell RR.
    Am J Med Genet; 1977; 1(2):195-205. PubMed ID: 416714
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  • 3. Morquio B syndrome: a primary defect in beta-galactosidase.
    van der Horst GT, Kleijer WJ, Hoogeveen AT, Huijmans JG, Blom W, van Diggelen OP.
    Am J Med Genet; 1983 Oct; 16(2):261-75. PubMed ID: 6418007
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  • 4. Beta galactosidase and the Morquio syndrome.
    Spranger JW.
    Am J Med Genet; 1977 Oct; 1(2):207-9. PubMed ID: 416715
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  • 6. Morquio-B disease, spondyloepiphyseal dysplasia associated with acid beta-galactosidase deficiency. Report of three cases in one family.
    van Gemund JJ, Giesberts MA, Eerdmans RF, Blom W, Kleijer WJ.
    Hum Genet; 1983 Oct; 64(1):50-4. PubMed ID: 6409799
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  • 7. [An atypical form of spondyle-epiphyseal dysostosis (pseudo-Morquio)].
    Boreaux G, Brocher JE, Klein D, Martin du Pan R.
    Fortschr Geb Rontgenstr Nuklearmed; 1970 Apr; 112(4):510-4. PubMed ID: 4998142
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  • 9. [Roentgenographic findings in mucopolysaccharidosis iv (morquio disease)].
    Ortlieb.
    Radiologe; 1975 Aug; 15(8):336-9. PubMed ID: 814582
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  • 12. The Morquio syndrome (MPS IV).
    Elliott DE, Kopits SE, Ozer FL.
    Birth Defects Orig Artic Ser; 1974 Aug; 10(12):458-64. PubMed ID: 4218785
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  • 13. Mucopolysaccharidosis type IV (Morquio syndrome).
    Singh MN, Agrawal A, Tilak V, Singh NK.
    J Assoc Physicians India; 2007 Jun; 55():434. PubMed ID: 17879498
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  • 15. A Korean patient with Morquio B disease with a novel c.13_14insA mutation in the GLB1 gene.
    Sohn YB, Park HD, Park SW, Kim SH, Cho SY, Ko AR, Ki CS, Yeau S, Jin DK.
    Ann Clin Lab Sci; 2012 Jun; 42(1):89-93. PubMed ID: 22371915
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  • 16. Dyggve disease.
    Barylak A, Kozlowski K.
    Aust Paediatr J; 1972 Dec; 8(6):338-41. PubMed ID: 4197473
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  • 17. Mutation analyses in 17 patients with deficiency in acid beta-galactosidase: three novel point mutations and high correlation of mutation W273L with Morquio disease type B.
    Paschke E, Milos I, Kreimer-Erlacher H, Hoefler G, Beck M, Hoeltzenbein M, Kleijer W, Levade T, Michelakakis H, Radeva B.
    Hum Genet; 2001 Aug; 109(2):159-66. PubMed ID: 11511921
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  • 18. Clinical and molecular analysis of a Japanese boy with Morquio B disease.
    Ishii N, Oohira T, Oshima A, Sakuraba H, Endo F, Matsuda I, Sukegawa K, Orii T, Suzuki Y.
    Clin Genet; 1995 Aug; 48(2):103-8. PubMed ID: 7586649
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