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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. Ann Hematol. 1992 Feb;64(2):88-92. doi: 10.1007/BF01715351. Ann Hematol. 1992. PMID: 1554800
[Aplastic crises in hereditary spherocytosis].
Pekrun A, Eiffert H, Eber SW, Schröter W. Pekrun A, et al. Among authors: eber sw. 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. Eur J Pediatr. 1988 Aug;147(6):639-42. doi: 10.1007/BF00442481. Eur J Pediatr. 1988. PMID: 3141191
Combined ankyrin and spectrin deficiency in hereditary spherocytosis.
Pekrun A, Eber SW, Kuhlmey A, Schröter W. Pekrun A, et al. Among authors: eber sw. Ann Hematol. 1993 Aug;67(2):89-93. doi: 10.1007/BF01788132. Ann Hematol. 1993. PMID: 8347735
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. J Pediatr. 1990 Sep;117(3):409-16. doi: 10.1016/s0022-3476(05)81081-9. J Pediatr. 1990. PMID: 2391596
[Disorders of the membrane skeleton of erythrocytes in hereditary spherocytosis and elliptocytosis: significance of the molecular defect for pathogenesis and clinical severity].
Eber SW. Eber SW. Klin Padiatr. 1991 Jul-Aug;203(4):284-95. doi: 10.1055/s-2007-1025443. Klin Padiatr. 1991. PMID: 1942935 Review. German.
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: eber sw. Ann Hematol. 1992 Feb;64(2):93-6. doi: 10.1007/BF01715352. Ann Hematol. 1992. PMID: 1554801
Frequency of very late fatal sepsis after splenectomy for hereditary spherocytosis: impact of insufficient antibody response to pneumococcal infection.
Eber SW, Langendörfer CM, Ditzig M, Reinhardt D, Stöhr G, Soldan W, Schröter W, Tchernia G. Eber SW, et al. Ann Hematol. 1999 Nov;78(11):524-8. doi: 10.1007/s002770050550. Ann Hematol. 1999. PMID: 10602897
A dispermic chimerism in a 2-year-old Caucasian boy.
Repas-Humpe LM, Humpe A, Lynen R, Glock B, Dauber EM, Simson G, Mayr WR, Köhler M, Eber S. Repas-Humpe LM, et al. Among authors: eber s. Ann Hematol. 1999 Sep;78(9):431-4. doi: 10.1007/s002770050543. Ann Hematol. 1999. PMID: 10525832
[Molecular pathology of the erythrocyte membrane. Erythrocyte membrane defects as a cause of congenital hemolytic anemia].
Schröter W, Eber SW. Schröter W, et al. Among authors: eber sw. Monatsschr Kinderheilkd. 1989 Jul;137(7):368-79. Monatsschr Kinderheilkd. 1989. PMID: 2677683 Review. German.
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