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Journal Abstract Search

143 related items for PubMed ID: 6883788

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  • 23. Sleep disturbances in aspartylglucosaminuria (AGU): a questionnaire study.
    Lindblom N, Kivinen S, Heiskala H, Laakso ML, Kaski M.
    J Inherit Metab Dis; 2006 Oct; 29(5):637-46. PubMed ID: 16944277
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  • 25. Aspartylglycosaminuria: a review.
    Arvio M, Mononen I.
    Orphanet J Rare Dis; 2016 Dec 01; 11(1):162. PubMed ID: 27906067
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  • 30. Dysmorphic facial features in aspartylglucosaminuria patients and carriers.
    Arvio MA, Peippo MM, Arvio PJ, Kääriäinen HA.
    Clin Dysmorphol; 2004 Jan 01; 13(1):11-5. PubMed ID: 15127757
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  • 31. Letter: Aspartylglycosaminuria in Northern Norway.
    Borud O, Torp KH.
    Lancet; 1976 May 15; 1(7968):1082-3. PubMed ID: 57494
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  • 34. Biochemical and structural insights into an allelic variant causing the lysosomal storage disorder - aspartylglucosaminuria.
    Pande S, Bizilj W, Guo HC.
    FEBS Lett; 2018 Aug 15; 592(15):2550-2561. PubMed ID: 29993127
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  • 39. Adenovirus-mediated gene transfer results in decreased lysosomal storage in brain and total correction in liver of aspartylglucosaminuria (AGU) mouse.
    Peltola M, Kyttälä A, Heinonen O, Rapola J, Paunio T, Revah F, Peltonen L, Jalanko A.
    Gene Ther; 1998 Oct 15; 5(10):1314-21. PubMed ID: 9930336
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  • 40. Aspartylglucosaminuria: psychomotor retardation masquerading as a mucopolysaccharidosis.
    Isenberg JN, Sharp HL.
    J Pediatr; 1975 May 15; 86(5):713-7. PubMed ID: 805826
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