Baerlocher K - Search Results

1

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

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

2

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. Helv Paediatr Acta. 1978 Dec;33(6):465-87. Helv Paediatr Acta. 1978. PMID: 738900

3

Infantile lactic acidosis due to hereditary fructose 1,6-diphosphatase deficiency.

Baerlocher K, Gitzelmann R, Nüssli R, Dumermuth G. Baerlocher K, et al. Helv Paediatr Acta. 1971 Dec;26(5):489-506. Helv Paediatr Acta. 1971. PMID: 4335192 No abstract available.

4

[Hereditary defects of fructose and galactose metabolism].

Gitzelmann R, Baerlocher K, Prader A. Gitzelmann R, et al. Among authors: baerlocher k. Monatsschr Kinderheilkd (1902). 1973 May;121(5):174-80. Monatsschr Kinderheilkd (1902). 1973. PMID: 4351554 German. No abstract available.

5

Hydantoin-5-propionic aciduria in folic acid nondependent formiminoglutamic aciduria observed in two siblings.

Niederwieser A, Matasović A, Steinmann B, Baerlocher K, Kempken B. Niederwieser A, et al. Among authors: baerlocher k. Pediatr Res. 1976 Apr;10(4):215-9. doi: 10.1203/00006450-197604000-00002. Pediatr Res. 1976. PMID: 1272625

6

Anomalous eosinophil granulocytes in blood and bone marrow: a diagnostic marker for infantile GM1-gangliosidosis?

Gitzelmann R, Spycher MA, Adank S, Baerlocher K, Steinmann B. Gitzelmann R, et al. Among authors: baerlocher k. Eur J Pediatr. 1985 May;144(1):82-4. doi: 10.1007/BF00491934. Eur J Pediatr. 1985. PMID: 3926503

7

Excretion of pterins in phenylketonuria and phenylketonuria variants.

Niederwieser A, Curtius HC, Gitzelmann R, Otten A, Baerlocher K, Blehovà B, Berlow S, Gröbe H, Rey F, Schaub J, Scheibenreiter S, Schmidt H, Viscontini M. Niederwieser A, et al. Among authors: baerlocher k. Helv Paediatr Acta. 1980 Sep;35(4):335-42. Helv Paediatr Acta. 1980. PMID: 7005193

8

Folic acid non-dependent formiminoglutamic aciduria in two siblings.

Niederwieser A, Giliberti P, Matasović A, Pluznik S, Steinmann B, Baerlocher K. Niederwieser A, et al. Among authors: baerlocher k. Clin Chim Acta. 1974 Aug 20;54(3):293-316. doi: 10.1016/0009-8981(74)90248-4. Clin Chim Acta. 1974. PMID: 4413489 No abstract available.

9

Short-chain acyl-CoA dehydrogenase deficiency in a 16-year-old girl with severe muscle wasting and scoliosis.

Baerlocher KE, Steinmann B, Aguzzi A, Krähenbühl S, Roe CR, Vianey-Saban C. Baerlocher KE, et al. J Inherit Metab Dis. 1997 Jul;20(3):427-31. doi: 10.1023/a:1005319120751. J Inherit Metab Dis. 1997. PMID: 9266373 No abstract available.

10

[The frequency of increased excretion of cystine among school children in Zürich].

Meier P, Rampini S, Baerlocher K, Prader A. Meier P, et al. Among authors: baerlocher k. Helv Paediatr Acta. 1974 Aug;29(3):237-44. Helv Paediatr Acta. 1974. PMID: 4849918 German. No abstract available.

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