Larsson A - Search Results

1

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. Mayatepek E, et al. Among authors: larsson a. J Inherit Metab Dis. 1995;18(1):83-4. doi: 10.1007/BF00711382. J Inherit Metab Dis. 1995. PMID: 7542714 No abstract available.

2

Deficient synthesis of cysteinyl leukotrienes in glutathione synthetase deficiency.

Mayatepek E, Becker K, Carlsson B, Larsson A, Hoffmann GF. Mayatepek E, et al. Among authors: larsson a. Int J Tissue React. 1993;15(6):245-52. Int J Tissue React. 1993. PMID: 8088946

3

5-Oxoprolinuria associated with 5-oxoprolinase deficiency; further evidence that this is a benign disorder.

Henderson MJ, Larsson A, Carlsson B, Dear PR. Henderson MJ, et al. Among authors: larsson a. J Inherit Metab Dis. 1993;16(6):1051-2. doi: 10.1007/BF00711529. J Inherit Metab Dis. 1993. PMID: 8127060 No abstract available.

4

Impaired synthesis of lipoxygenase products in glutathione synthetase deficiency.

Mayatepek E, Hoffmann GF, Carlsson B, Larsson A, Becker K. Mayatepek E, et al. Among authors: larsson a. Pediatr Res. 1994 Mar;35(3):307-10. doi: 10.1203/00006450-199403000-00005. Pediatr Res. 1994. PMID: 8190517

5

Long-term clinical outcome in patients with glutathione synthetase deficiency.

Ristoff E, Mayatepek E, Larsson A. Ristoff E, et al. Among authors: larsson a. J Pediatr. 2001 Jul;139(1):79-84. doi: 10.1067/mpd.2001.114480. J Pediatr. 2001. PMID: 11445798

6

Massive 5-oxoprolinuria with normal 5-oxoprolinase and glutathione synthetase activities.

Riudor E, Arranz JA, Alvarez R, Carlsson K, del Toro M, Salmerón F, Piñol F, Ristoff E, Sentis M, Larsson A. Riudor E, et al. Among authors: larsson a. J Inherit Metab Dis. 2001 Jun;24(3):404-6. doi: 10.1023/a:1010569021839. J Inherit Metab Dis. 2001. PMID: 11486906 No abstract available.

7

Oxidative stress in inborn errors of metabolism: lessons from glutathione deficiency.

Ristoff E, Larsson A. Ristoff E, et al. Among authors: larsson a. J Inherit Metab Dis. 2002 May;25(3):223-6. doi: 10.1023/a:1015634032042. J Inherit Metab Dis. 2002. PMID: 12137231 Review.

8

5-Oxoprolinuria (glutathione synthetase deficiency): a case with neonatal presentation and rapid fatal outcome.

Divry P, Roulaud-Parrot F, Dorche C, Zabot MT, Contraire B, Hagenfeldt L, Larsson A. Divry P, et al. Among authors: larsson a. J Inherit Metab Dis. 1991;14(3):341-4. doi: 10.1007/BF01811698. J Inherit Metab Dis. 1991. PMID: 1770788 No abstract available.

9

Generalized glutathione synthetase deficiency and pregnancy.

Ristoff E, Augustson C, Larsson A. Ristoff E, et al. Among authors: larsson a. J Inherit Metab Dis. 1999 Aug;22(6):758-9. doi: 10.1023/a:1005564705898. J Inherit Metab Dis. 1999. PMID: 10472538 No abstract available.

10

Glutathione synthetase deficiency associated with antenatal cerebral bleeding.

Brüggemann LW, Groenendaal F, Ristoff E, Larsson A, Duran M, van Lier JA, Dorland L, Berger R, de Koning TJ. Brüggemann LW, et al. Among authors: larsson a. J Inherit Metab Dis. 2004;27(2):275-6. doi: 10.1023/b:boli.0000028844.84760.a1. J Inherit Metab Dis. 2004. PMID: 15243982

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