These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

73 related items for PubMed ID: 2842830

  • 21. 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; 8(4):212-8. PubMed ID: 3939546
    [Abstract] [Full Text] [Related]

  • 22. Liquid-chromatographic detection of aspartylglycosaminuria.
    Mononen T, Parviainen M, Penttilä I, Mononen I.
    Clin Chem; 1986 Mar; 32(3):501-2. PubMed ID: 3948393
    [Abstract] [Full Text] [Related]

  • 23. Aspartylglucosaminuria: unusual neonatal presentation in Qatari twins with a novel aspartylglucosaminidase gene mutation and 3 new cases in a Turkish family.
    Opladen T, Ebinger F, Zschocke J, Sengupta D, Ben-Omran T, Shahbeck N, Moog U, Fischer C, Bürger F, Haas D, Ruef P, Harting I, Al-Rifai H, Hoffmann GF.
    J Child Neurol; 2014 Jan; 29(1):36-42. PubMed ID: 23271757
    [Abstract] [Full Text] [Related]

  • 24. 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
    [Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26. Letter: Aspartylglycosaminuria in Northern Norway.
    Borud O, Torp KH.
    Lancet; 1976 May 15; 1(7968):1082-3. PubMed ID: 57494
    [No Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 29.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 30. Aspartylglucosamine excretion in heterozygous carriers of aspartylglycosaminuria.
    Mononen TK.
    Clin Chim Acta; 1989 Mar 15; 180(1):99-101. PubMed ID: 2743573
    [No Abstract] [Full Text] [Related]

  • 31.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33. Urinary oligosaccharide excretion in disorders of glycolipid, glycoprotein and glycogen metabolism. A review of screening for differential diagnosis.
    Sewell AC.
    Eur J Pediatr; 1980 Sep 15; 134(3):183-94. PubMed ID: 6775948
    [Abstract] [Full Text] [Related]

  • 34. Aspartylglycosaminuria: a gargoyle-like syndrome with autosomal recessive inheritance.
    Autio S, Palo J, Perheentupa J.
    Birth Defects Orig Artic Ser; 1974 Sep 15; 10(4):193-200. PubMed ID: 4220085
    [Abstract] [Full Text] [Related]

  • 35. Aspartylglucosaminuria: psychomotor retardation masquerading as a mucopolysaccharidosis.
    Isenberg JN, Sharp HL.
    J Pediatr; 1975 May 15; 86(5):713-7. PubMed ID: 805826
    [Abstract] [Full Text] [Related]

  • 36. Letter: Leukocyte function in aspartylglucosaminuria.
    Fleisher TA, Isenberg JN, Sharp HL.
    J Pediatr; 1975 Nov 15; 87(5):833. PubMed ID: 1185361
    [No Abstract] [Full Text] [Related]

  • 37. Toward understanding the neuronal pathogenesis of aspartylglucosaminuria: expression of aspartylglucosaminidase in brain during development.
    Uusitalo A, Tenhunen K, Heinonen O, Hiltunen JO, Saarma M, Haltia M, Jalanko A, Peltonen L.
    Mol Genet Metab; 1999 Aug 15; 67(4):294-307. PubMed ID: 10444340
    [Abstract] [Full Text] [Related]

  • 38.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. Mucolipidosis III type C: first-trimester biochemical and molecular prenatal diagnosis.
    Falik-Zaccai TC, Zeigler M, Bargal R, Bach G, Borochowitz Z, Raas-Rothschild A.
    Prenat Diagn; 2003 Mar 15; 23(3):211-4. PubMed ID: 12627421
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 4.