Lundin G - Search Results

1

Genetic heterogeneity of the porphobilinogen deaminase gene in Swedish families with acute intermittent porphyria.

Lee JS, Lundin G, Lannfelt L, Forsell L, Picat C, Grandchamp B, Anvret M. Lee JS, et al. Among authors: lundin g. Hum Genet. 1991 Aug;87(4):484-8. doi: 10.1007/BF00197173. Hum Genet. 1991. PMID: 1679034

2

[Mutation diagnosis is a possibility for the half of the families with acute intermittent porphyria].

Anvret M, Lee JS, Lundin G. Anvret M, et al. Among authors: lundin g. Lakartidningen. 1991 Jul 24;88(30-31):2513-4. Lakartidningen. 1991. PMID: 1865718 Swedish. No abstract available.

3

Genetic carrier detection in Norwegian families with acute intermittent porphyria.

Sagen E, Laegreid A, Anvret M, Lundin G, Lannfelt L, Lilius L, Floderus Y, Romslo I. Sagen E, et al. Among authors: lundin g. Scand J Clin Lab Invest. 1993 Nov;53(7):687-91. doi: 10.3109/00365519309092572. Scand J Clin Lab Invest. 1993. PMID: 7903821

4

Two new mutations in the porphobilinogen deaminase gene and a screening method using PCR amplification of specific alleles.

Lundin G, Wedell A, Thunell S, Anvret M. Lundin G, et al. Hum Genet. 1994 Jan;93(1):59-62. doi: 10.1007/BF00218914. Hum Genet. 1994. PMID: 8270256

5

Four mutations in the porphobilinogen deaminase gene in patients with acute intermittent porphyria.

Lundin G, Hashemi J, Floderus Y, Thunell S, Sagen E, Laegreid A, Wassif W, Peters T, Anvret M. Lundin G, et al. J Med Genet. 1995 Dec;32(12):979-81. doi: 10.1136/jmg.32.12.979. J Med Genet. 1995. PMID: 8825929 Free PMC article.

6

Characterization and regulation of the nonerythroid porphobilinogen deaminase promoter.

Lundin G, Anvret M. Lundin G, et al. Biochem Biophys Res Commun. 1997 Feb 13;231(2):409-11. doi: 10.1006/bbrc.1997.6114. Biochem Biophys Res Commun. 1997. PMID: 9070289

7

Genetic investigation of the porphobilinogen deaminase gene in Swedish acute intermittent porphyria families.

Lundin G, Lee JS, Thunell S, Anvret M. Lundin G, et al. Hum Genet. 1997 Jul;100(1):63-6. doi: 10.1007/s004390050466. Hum Genet. 1997. PMID: 9225970

8

Diagnosis of acute intermittent porphyria in northern Sweden: an evaluation of mutation analysis and biochemical methods.

Andersson C, Thunell S, Floderus Y, Forsell C, Lundin G, Anvret M, Lannfelt L, Wetterberg L, Lithner F. Andersson C, et al. Among authors: lundin g. J Intern Med. 1995 Mar;237(3):301-8. doi: 10.1111/j.1365-2796.1995.tb01179.x. J Intern Med. 1995. PMID: 7891051

9

Strategy for highly selective ion-exchange capture using a charge-polarizing fusion partner.

Gräslund T, Ehn M, Lundin G, Hedhammar M, Uhlén M, Nygren PA, Hober S. Gräslund T, et al. Among authors: lundin g. J Chromatogr A. 2002 Jan 4;942(1-2):157-66. doi: 10.1016/s0021-9673(01)01413-3. J Chromatogr A. 2002. PMID: 11822381

10

Serum levels of the low molecular weight form of insulin-like growth factor binding protein in healthy subjects and patients with growth hormone deficiency, acromegaly and anorexia nervosa.

Hall K, Lundin G, Póvoa G. Hall K, et al. Among authors: lundin g. Acta Endocrinol (Copenh). 1988 Jul;118(3):321-6. doi: 10.1530/acta.0.1180321. Acta Endocrinol (Copenh). 1988. PMID: 2455950

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