Steinmann B - Search Results

1

Patients with hereditary fructose intolerance have normal erythrocyte aldolase activity.

Gitzelmann R, Steinmann B, Tuchschmid P. Gitzelmann R, et al. Among authors: steinmann b. Clin Chim Acta. 1989 May 15;181(2):163-6. doi: 10.1016/0009-8981(89)90183-6. Clin Chim Acta. 1989. PMID: 2736779

2

The diagnosis of hereditary fructose intolerance.

Steinmann B, Gitzelmann R. Steinmann B, et al. Helv Paediatr Acta. 1981 Sep;36(4):297-316. Helv Paediatr Acta. 1981. PMID: 6268573

3

Hereditary fructose intolerance in early childhood: a major diagnostic challenge. Survey of 20 symptomatic cases.

Baerlocher K, Gitzelmann R, Steinmann B, Gitzelmann-Cumarasamy N. Baerlocher K, et al. Among authors: steinmann b. Helv Paediatr Acta. 1978 Dec;33(6):465-87. Helv Paediatr Acta. 1978. PMID: 738900

4

Essential fructosuria: increased levels of fructose 3-phosphate in erythrocytes.

Petersen A, Steinmann B, Gitzelmann R. Petersen A, et al. Among authors: steinmann b. Enzyme. 1992;46(6):319-23. doi: 10.1159/000468811. Enzyme. 1992. PMID: 1308858

5

Ehlers-Danlos syndrome type IV: a multi-exon deletion in one of the two COL3A1 alleles affecting structure, stability, and processing of type III procollagen.

Superti-Furga A, Gugler E, Gitzelmann R, Steinmann B. Superti-Furga A, et al. Among authors: steinmann b. J Biol Chem. 1988 May 5;263(13):6226-32. J Biol Chem. 1988. PMID: 2834369 Free article.

6

Antibody activation of mutant human fructosediphosphate aldolase B in liver extracts of patients with hereditary fructose intolerance.

Gitzelmann R, Steinmann B, Bally C, Lebherz HG. Gitzelmann R, et al. Among authors: steinmann b. Biochem Biophys Res Commun. 1974 Aug 19;59(4):1270-7. doi: 10.1016/0006-291x(74)90451-3. Biochem Biophys Res Commun. 1974. PMID: 4212946 No abstract available.

7

Hepatic glycogen synthetase deficiency not expressed in cultured skin fibroblasts.

Gitzelmann R, Steinmann B, Aynsley-Green A. Gitzelmann R, et al. Among authors: steinmann b. Clin Chim Acta. 1983 May 9;130(1):111-5. doi: 10.1016/0009-8981(83)90264-4. Clin Chim Acta. 1983. PMID: 6406107

8

[Infusion-associated kidney and liver failure in undiagnosed hereditary fructose intolerance].

Müller-Wiefel DE, Steinmann B, Holm-Hadulla M, Wille L, Schärer K, Gitzelmann R. Müller-Wiefel DE, et al. Among authors: steinmann b. Dtsch Med Wochenschr. 1983 Jun 24;108(25):985-9. doi: 10.1055/s-2008-1069680. Dtsch Med Wochenschr. 1983. PMID: 6851900 German.

9

Changes of liver metabolite concentrations in adults with disorders of fructose metabolism after intravenous fructose by 31P magnetic resonance spectroscopy.

Boesiger P, Buchli R, Meier D, Steinmann B, Gitzelmann R. Boesiger P, et al. Among authors: steinmann b. Pediatr Res. 1994 Oct;36(4):436-40. doi: 10.1203/00006450-199410000-00004. Pediatr Res. 1994. PMID: 7816517 Clinical Trial.

10

[Hereditary disorders of fructose metabolism. Loading tests with fructose, sorbitol and dihydroxyacetone].

Steinmann B, Baerlocher K, Gitzelmann R. Steinmann B, et al. Nutr Metab. 1975;18 Suppl 1:115-32. Nutr Metab. 1975. PMID: 170564 German. No abstract available.

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