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Prevalence of increased osmotic fragility of erythrocytes in German blood donors: screening using a modified glycerol lysis test.
Eber SW, Pekrun A, Neufeldt A, Schröter W. Eber SW, et al. Among authors: schroter w. Ann Hematol. 1992 Feb;64(2):88-92. doi: 10.1007/BF01715351. Ann Hematol. 1992. PMID: 1554800
Triosephosphate isomerase deficiency: haemolytic anaemia, myopathy with altered mitochondria and mental retardation due to a new variant with accelerated enzyme catabolism and diminished specific activity.
Eber SW, Pekrun A, Bardosi A, Gahr M, Krietsch WK, Krüger J, Matthei R, Schröter W. Eber SW, et al. Among authors: schroter w. Eur J Pediatr. 1991 Sep;150(11):761-6. doi: 10.1007/BF02026706. Eur J Pediatr. 1991. PMID: 1959537
Membrane-bound 2,3-diphosphoglycerate phosphatase of human erythrocytes.
Schröter W, Neuvians M. Schröter W, et al. J Membr Biol. 1970 Dec;2(1):31-40. doi: 10.1007/BF01869848. J Membr Biol. 1970. PMID: 24174135
[Aplastic crises in hereditary spherocytosis].
Pekrun A, Eiffert H, Eber SW, Schröter W. Pekrun A, et al. Among authors: schroter w. Monatsschr Kinderheilkd. 1988 Apr;136(4):173-5. Monatsschr Kinderheilkd. 1988. PMID: 2838746 German.
Glucuronyl transferase deficiency and mild hereditary spherocytosis: effect of splenectomy.
Eber SW, Ullrich D, Speer CP, Armbrust R, Schröter W. Eber SW, et al. Among authors: schroter w. Eur J Pediatr. 1988 Aug;147(6):639-42. doi: 10.1007/BF00442481. Eur J Pediatr. 1988. PMID: 3141191
Variable clinical severity of hereditary spherocytosis: relation to erythrocytic spectrin concentration, osmotic fragility, and autohemolysis.
Eber SW, Armbrust R, Schröter W. Eber SW, et al. Among authors: schroter w. J Pediatr. 1990 Sep;117(3):409-16. doi: 10.1016/s0022-3476(05)81081-9. J Pediatr. 1990. PMID: 2391596
Absence of phosphorylation-induced gelation of erythrocyte membrane skeletons: a diagnostic tool for hereditary spherocytosis.
Armbrust R, Eber SW, Schröter W. Armbrust R, et al. Among authors: schroter w. Ann Hematol. 1992 Feb;64(2):93-6. doi: 10.1007/BF01715352. Ann Hematol. 1992. PMID: 1554801
Mutations in the R-type pyruvate kinase gene and altered enzyme kinetic properties in patients with hemolytic anemia due to pyruvate kinase deficiency.
Lakomek M, Huppke P, Neubauer B, Pekrun A, Winkler H, Schröter W. Lakomek M, et al. Among authors: schroter w. Ann Hematol. 1994 Nov;69(5):253-60. doi: 10.1007/BF01700280. Ann Hematol. 1994. PMID: 7948315
The gamma-chain heterogeneity of haemoglobin F in German infants.
Pekrun A, Scharnetzky M, Gahr M, Schröter W. Pekrun A, et al. Among authors: schroter w. Eur J Pediatr. 1989 Jan;148(4):304-6. doi: 10.1007/BF00444119. Eur J Pediatr. 1989. PMID: 2468496
Hemoglobin F in myelodysplastic syndrome.
Reinhardt D, Haase D, Schoch C, Wollenweber S, Hinkelmann E, v Heyden W, Lentini G, Wörmann B, Schröter W, Pekrun A. Reinhardt D, et al. Among authors: schroter w. Ann Hematol. 1998 Mar-Apr;76(3-4):135-8. doi: 10.1007/s002770050377. Ann Hematol. 1998. PMID: 9619730
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