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PUBMED FOR HANDHELDS

Journal Abstract Search


143 related items for PubMed ID: 6883788

  • 1. Aspartylglucosaminuria in the United States.
    Hreidarsson S, Thomas GH, Valle DL, Stevenson RE, Taylor H, McCarty J, Coker SB, Green WR.
    Clin Genet; 1983 Jun; 23(6):427-35. PubMed ID: 6883788
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  • 2. Progressive nature of aspartylglucosaminuria.
    Arvio P, Arvio M.
    Acta Paediatr; 2002 Jun; 91(3):255-7. PubMed ID: 12022293
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  • 3. Aspartylglucosaminuria among Palestinian Arabs.
    Zlotogora J, Ben-Neriah Z, Abu-Libdeh BY, Sury V, Zeigler M.
    J Inherit Metab Dis; 1997 Nov; 20(6):799-802. PubMed ID: 9427148
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  • 4. [Aspartylglucosaminuria. Clinical description of 2 German patients].
    Ziegler R, Schmidt H, Sewell AC, Weglage J, von Lengerke JH, Ullrich K.
    Monatsschr Kinderheilkd; 1989 Aug; 137(8):454-7. PubMed ID: 2811876
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  • 5. Disturbed metabolism of copper and zinc in aspartylglycosaminuria: possible involvement with connective tissue changes.
    Näntö-Salonen K, Halme T, Penttinen R, Langevelde FV, Vis RD, Alfthan G.
    J Inherit Metab Dis; 1985 Aug; 8(4):212-8. PubMed ID: 3939546
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  • 10. Recent findings on some "new" neurometabolic diseases.
    Palo J, Santavuori P, Haltia M.
    Riv Patol Nerv Ment; 1976 Aug; 97(4):191-8. PubMed ID: 1032035
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  • 12. Picture of the Month. Aspartylglucosaminuria.
    Palo J, Autio S.
    Am J Dis Child; 1974 Apr; 127(4):561-2. PubMed ID: 4821322
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  • 13. Mice with an aspartylglucosaminuria mutation similar to humans replicate the pathophysiology in patients.
    Jalanko A, Tenhunen K, McKinney CE, LaMarca ME, Rapola J, Autti T, Joensuu R, Manninen T, Sipilä I, Ikonen S, Riekkinen P, Ginns EI, Peltonen L.
    Hum Mol Genet; 1998 Feb; 7(2):265-72. PubMed ID: 9425233
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  • 19. Screening of inherited oligosaccharidurias among mentally retarded patients in northern Finland.
    Aula P, Renlund M, Raivio KO, Koskela SL.
    J Ment Defic Res; 1986 Dec; 30 ( Pt 4)():365-8. PubMed ID: 3806663
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  • 20. Prenatal diagnosis and fetal pathology of aspartylglucosaminuria.
    Aula P, Rapola J, von Koskull H, Ammälä P.
    Am J Med Genet; 1984 Oct; 19(2):359-67. PubMed ID: 6507482
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