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25. Transient 5-oxoprolinuria: unusually high anion gap acidosis in an infant. Hulley SL; Perring J; Manning N; Olpin S; Yap S Eur J Pediatr; 2015 Dec; 174(12):1685-8. PubMed ID: 26122794 [TBL] [Abstract][Full Text] [Related]
26. Ophthalmological, psychometric and therapeutic investigation in two sisters with hereditary glutathione synthetase deficiency (5-oxoprolinuria). Larsson A; Wachtmeister L; von Wendt L; Andersson R; Hagenfeldt L; Herrin KM Neuropediatrics; 1985 Aug; 16(3):131-6. PubMed ID: 4047346 [TBL] [Abstract][Full Text] [Related]
27. Transient 5-oxoprolinuria (pyroglutamic aciduria) with systemic acidosis in an adult receiving antibiotic therapy. Croal BL; Glen AC; Kelly CJ; Logan RW Clin Chem; 1998 Feb; 44(2):336-40. PubMed ID: 9474033 [TBL] [Abstract][Full Text] [Related]
28. A therapeutic trial with N-acetylcysteine in subjects with hereditary glutathione synthetase deficiency (5-oxoprolinuria). Mårtensson J; Gustafsson J; Larsson A J Inherit Metab Dis; 1989; 12(2):120-30. PubMed ID: 2502672 [TBL] [Abstract][Full Text] [Related]
29. New aspects of glutathione biochemistry and transport--selective alteration of glutathione metabolism. Meister A Nutr Rev; 1984 Dec; 42(12):397-410. PubMed ID: 6151157 [No Abstract] [Full Text] [Related]
30. Glutathione synthetase deficiency: a family report. Pejaver RK; Watson AH J R Soc Med; 1994 Mar; 87(3):171. PubMed ID: 8158601 [TBL] [Abstract][Full Text] [Related]
31. The metabolic formation and utilization of 5-oxo-L-proline (L-pyroglutamate, L-pyrrolidone carboxylate). van der Werf P; Meister A Adv Enzymol Relat Areas Mol Biol; 1975; 43():519-56. PubMed ID: 1106127 [No Abstract] [Full Text] [Related]
32. Treatment of glutathione peroxidase deficiency with vitamin E. Nutr Rev; 1980 Mar; 38(3):120-2. PubMed ID: 7375069 [No Abstract] [Full Text] [Related]
33. Relation between ataxia and defects of the gamma-glutamyl cycle. Meister A Adv Neurol; 1978; 21():289-302. PubMed ID: 32746 [No Abstract] [Full Text] [Related]
34. [Glutathion-synthetase deficiency with 5-oxoprolinuria. Two new cases and a review of the literature (author's transl)]. Boivin P; Galand C; Schaison G Nouv Presse Med; 1978 May; 7(18):1531-5. PubMed ID: 673703 [TBL] [Abstract][Full Text] [Related]
35. 5-Oxoprolinase deficiency associated with severe psychomotor developmental delay, failure to thrive, microcephaly and microcytic anaemia. Mayatepek E; Hoffmann GF; Larsson A; Becker K; Bremer HJ J Inherit Metab Dis; 1995; 18(1):83-4. PubMed ID: 7542714 [No Abstract] [Full Text] [Related]
36. What is the clinical significance of 5-oxoproline (pyroglutamic acid) in high anion gap metabolic acidosis following paracetamol (acetaminophen) exposure? Liss DB; Paden MS; Schwarz ES; Mullins ME Clin Toxicol (Phila); 2013 Nov; 51(9):817-27. PubMed ID: 24111553 [TBL] [Abstract][Full Text] [Related]
37. Enhancement of glutathione content in glutathione synthetase-deficient fibroblasts from a patient with 5-oxoprolinuria via metabolic cooperation with normal fibroblasts. Kavanagh TJ; Raghu G; White CC; Martin GM; Rabinovitch PS; Eaton DL Exp Cell Res; 1994 May; 212(1):69-76. PubMed ID: 7909755 [TBL] [Abstract][Full Text] [Related]
38. A case of severe glutathione synthetase deficiency with novel GSS mutations. Xia H; Ye J; Wang L; Zhu J; He Z Braz J Med Biol Res; 2018 Jan; 51(3):e6853. PubMed ID: 29340523 [TBL] [Abstract][Full Text] [Related]
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40. Hereditary non-spherocytic haemolytic anaemia due to red blood cell glutathione synthetase deficiency in four unrelated patients from Spain: clinical and molecular studies. Corrons JL; Alvarez R; Pujades A; Zarza R; Oliva E; Lasheras G; Callis M; Ribes A; Gelbart T; Beutler E Br J Haematol; 2001 Feb; 112(2):475-82. PubMed ID: 11167850 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]