Floderus Y - Search Results

1

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: floderus y. J Intern Med. 1995 Mar;237(3):301-8. doi: 10.1111/j.1365-2796.1995.tb01179.x. J Intern Med. 1995. PMID: 7891051

2

Liver transplantation in a boy with acute porphyria due to aminolaevulinate dehydratase deficiency.

Thunell S, Henrichson A, Floderus Y, Groth CG, Eriksson BG, Barkholt L, Nemeth A, Strandvik B, Eleborg L, Holmberg L, et al. Thunell S, et al. Among authors: floderus y. Eur J Clin Chem Clin Biochem. 1992 Oct;30(10):599-606. doi: 10.1515/cclm.1992.30.10.599. Eur J Clin Chem Clin Biochem. 1992. PMID: 1493152

3

Alcoholic beverages in acute porphyria.

Thunell S, Floderus Y, Henrichson A, Moore MR, Meissner P, Sinclair J. Thunell S, et al. Among authors: floderus y. J Stud Alcohol. 1992 May;53(3):272-6. doi: 10.15288/jsa.1992.53.272. J Stud Alcohol. 1992. PMID: 1583906

4

Porphobilinogen deaminase in acute intermittent porphyria: activity and concentration in erythrocytes and lymphocytes.

Lilius L, Lannfelt L, Wetterberg L, Floderus Y, Henrichson A, Thunell S. Lilius L, et al. Among authors: floderus y. Clin Chim Acta. 1991 Feb 28;197(1):77-84. doi: 10.1016/0009-8981(91)90350-l. Clin Chim Acta. 1991. PMID: 2044216 No abstract available.

5

Mutations in acute intermittent porphyria detected by ELISA measurement of porphobilinogen deaminase.

Lannfelt L, Wetterberg L, Gellerfors P, Lilius L, Floderus Y, Thunell S. Lannfelt L, et al. Among authors: floderus y. J Clin Chem Clin Biochem. 1989 Nov;27(11):857-62. doi: 10.1515/cclm.1989.27.11.857. J Clin Chem Clin Biochem. 1989. PMID: 2607315

6

DNA polymorphisms within the porphobilinogen deaminase gene in two Swedish families with acute intermittent porphyria.

Lee JS, Anvret M, Lindsten J, Lannfelt L, Gellerfors P, Wetterberg L, Floderus Y, Thunell S. Lee JS, et al. Among authors: floderus y. Hum Genet. 1988 Aug;79(4):379-81. doi: 10.1007/BF00282182. Hum Genet. 1988. PMID: 2900803

7

Genetic regulation of the red cell uroporphyrinogen-I-synthetase level in families with acute intermittent porphyria.

Wetterberg L, Floderus Y, Thunell S, Iselius L, Lindsten J. Wetterberg L, et al. Among authors: floderus y. Clin Genet. 1983 Dec;24(6):403-6. doi: 10.1111/j.1399-0004.1983.tb00094.x. Clin Genet. 1983. PMID: 6652953

8

Erythrocyte catechol-O-methyltransferase activity in related families with schizophrenia.

Floderus Y, Böök JA, Wetterberg L. Floderus Y, et al. Clin Genet. 1981 May;19(5):379-85. doi: 10.1111/j.1399-0004.1981.tb00729.x. Clin Genet. 1981. PMID: 7296926 No abstract available.

9

Erythrocyte catechol-O-methyltransferase activity in a Swedish population.

Floderus Y, Ross SB, Wetterberg L. Floderus Y, et al. Clin Genet. 1981 May;19(5):389-92. doi: 10.1111/j.1399-0004.1981.tb00731.x. Clin Genet. 1981. PMID: 7296928

10

The inheritance of human erythrocyte catechol-O-methyltransferase activity.

Floderus Y, Wetterberg L. Floderus Y, et al. Clin Genet. 1981 May;19(5):392-5. doi: 10.1111/j.1399-0004.1981.tb00732.x. Clin Genet. 1981. PMID: 7296929 No abstract available.

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