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121 related items for PubMed ID: 7357836
21. Amniotic fluid glycoasparagines in fetal aspartylglycosaminuria. Mononen I, Kaartinen V, Mononen T. J Inherit Metab Dis; 1988; 11(2):194-8. PubMed ID: 3139932 [Abstract] [Full Text] [Related]
22. Aspartylglycosaminuria, urinary excretion of aspartylglycosamines related to mental retardation. Borud O, Torp KH, Dahl T. Monogr Hum Genet; 1978; 10():23-6. PubMed ID: 723900 [No Abstract] [Full Text] [Related]
23. Characterization of two glycoasparagines isolated from the urine of patients with aspartylglycosylaminuria (AGU). Sugahara K, Funakoshi S, Funakoshi I, Aula P, Yamashina I. J Biochem; 1975 Oct; 78(4):673-8. PubMed ID: 1213985 [Abstract] [Full Text] [Related]
24. Extra heating of TLC plates detects two lysosomal storage diseases, aspartylglucosaminuria and fucosidosis, during routine urinary amino acid screening. Simell O, Sipilä I, Autio S. Clin Chim Acta; 1983 Sep 30; 133(2):227-32. PubMed ID: 6627685 [No Abstract] [Full Text] [Related]
26. Aspartylglucosaminuria: psychomotor retardation masquerading as a mucopolysaccharidosis. Isenberg JN, Sharp HL. J Pediatr; 1975 May 22; 86(5):713-7. PubMed ID: 805826 [Abstract] [Full Text] [Related]
27. Accumulation of two glycoasparagines in the liver in aspartylglycosaminuria. Maury P. J Biol Chem; 1979 Mar 10; 254(5):1513-5. PubMed ID: 762149 [Abstract] [Full Text] [Related]
28. Dissection of the molecular pathology of aspartylglucosaminuria provides the basis for DNA diagnostics and future therapeutic interventions. Ikonen E, Syvänen AC, Peltonen L. Scand J Clin Lab Invest Suppl; 1993 Mar 10; 213():19-27. PubMed ID: 8322015 [Abstract] [Full Text] [Related]
29. Human leukocyte glycosylasparaginase: cell-to-cell transfer and properties in correction of aspartylglycosaminuria. Dunder U, Mononen I. FEBS Lett; 2001 Jun 15; 499(1-2):77-81. PubMed ID: 11418116 [Abstract] [Full Text] [Related]
30. High prevalence of aspartylglycosaminuria among school-age children in eastern Finland. Mononen T, Mononen I, Matilainen R, Airaksinen E. Hum Genet; 1991 Jul 15; 87(3):266-8. PubMed ID: 1864600 [Abstract] [Full Text] [Related]
31. 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]
32. The glycoasparagines in urine of a patient with aspartylglycosaminuria. Pollitt RJ, Pretty KM. Biochem J; 1974 Jul 15; 141(1):141-6. PubMed ID: 4455197 [Abstract] [Full Text] [Related]
33. A fluorometric assay for glycosylasparaginase activity and detection of aspartylglycosaminuria. Mononen IT, Kaartinen VM, Williams JC. Anal Biochem; 1993 Feb 01; 208(2):372-4. PubMed ID: 8452235 [Abstract] [Full Text] [Related]
34. Copper and zinc metabolism in aspartylglycosaminuria and Salla disease. van Langevelde F, Vis RD, Näntö-Salonen K, Halme T, Pakarinen P, Hyörä H, Vuorinen K, Näntö V. Sci Total Environ; 1985 Mar 15; 42(1-2):171-80. PubMed ID: 4012278 [Abstract] [Full Text] [Related]
35. Aspartylglycosaminuria: a review. Arvio M, Mononen I. Orphanet J Rare Dis; 2016 Dec 01; 11(1):162. PubMed ID: 27906067 [Abstract] [Full Text] [Related]
36. Enzymatic diagnosis and carrier detection of aspartylglucosaminuria using blood samples. Aula P, Raivio K, Autio S. Pediatr Res; 1976 Jun 01; 10(6):625-9. PubMed ID: 1272639 [Abstract] [Full Text] [Related]
37. Enzymatic determination of urinary aspartylglycosylamine: a rapid and sensitive-method to detect aspartylclycosylaminuria (AGU). Sugahara K, Nishimura K, Aula P, Yamashina IY. Clin Chim Acta; 1976 Oct 15; 72(2):265-7. PubMed ID: 987869 [No Abstract] [Full Text] [Related]