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Results:
1-19
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Results: 19
Authors:
Kveder, V
Kittler, M
Schroter, W
Citation: V. Kveder et al., Recombination activity of contaminated dislocations in silicon: A electron-beam-induced current contrast behavior - art. no. 115208, PHYS REV B, 6311(11), 2001, pp. 5208
Authors:
Kugler, W
Willaschek, C
Holtz, C
Ohlenbusch, A
Laspe, P
Krugener, R
Muirhead, H
Schroter, W
Lakomek, M
Citation: W. Kugler et al., Eight novel mutations and consequences on mRNA and protein level in pyruvate kinase-deficient patients with nonspherocytic hemolytic anemia, HUM MUTAT, 15(3), 2000, pp. 261-272
Authors:
Schroter, W
Kveder, V
Seibt, M
Ewe, H
Hedemann, H
Riedel, F
Sattler, A
Citation: W. Schroter et al., Atomic structure and electronic states of nickel and copper silicides in silicon, MAT SCI E B, 72(2-3), 2000, pp. 80-86
Authors:
Kveder, V
Schroter, W
Sattler, A
Seibt, M
Citation: V. Kveder et al., Simulation of Al and phosphorus diffusion gettering in Si, MAT SCI E B, 71, 2000, pp. 175-181
Authors:
Mesli, A
Schroter, W
Weber, J
Citation: A. Mesli et al., Containing Papers Presented at the European Materials Research Society 1999 Spring Meeting, Symposium F: Process Induced Defects in Semiconductors, June 1-4, 1999, Strasbourg, France - Preface, MAT SCI E B, 71, 2000, pp. IX-IX
Authors:
Riedel, F
Schroter, W
Citation: F. Riedel et W. Schroter, Electrical and structural properties of nanoscale NiSi2 precipitates in silicon, PHYS REV B, 62(11), 2000, pp. 7150-7156
Authors:
Roth, C
Bokemeier, M
Bartz, M
Leonhardt, U
Erdlenbruch, B
Schroter, W
Pekrun, A
Citation: C. Roth et al., Glucose tolerance disorders in patients suffering from thalassemia major, MONATS KIND, 148(12), 2000, pp. 1092-1097
Authors:
Myers, SM
Seibt, M
Schroter, W
Citation: Sm. Myers et al., Mechanisms of transition-metal gettering in silicon, J APPL PHYS, 88(7), 2000, pp. 3795-3819
Authors:
Iglauer, A
Reinhardt, D
Schroter, W
Pekrun, A
Citation: A. Iglauer et al., Cryohemolysis test as a diagnostic tool for hereditary spherocytosis, ANN HEMATOL, 78(12), 1999, pp. 555-557
Authors:
Eber, SW
Langendorfer, CM
Ditzig, M
Reinhardt, D
Stohr, G
Soldan, W
Schroter, W
Tchernia, G
Citation: Sw. Eber et al., Frequency of very late fatal sepsis after splenectomy for hereditary spherocytosis: impact of insufficient antibody response to pneumococcal infection, ANN HEMATOL, 78(11), 1999, pp. 524-528
Authors:
Lenz, E
Repas-Humpe, M
Oldenburg, J
Kreuz, W
Schroter, W
Eber, SW
Citation: E. Lenz et al., Therapy-resistant haemarthros in a patient with factor VIII inhibitor: successful treatment with recombinant factor VIIa, EUR J PED, 158(11), 1999, pp. 951-952
Authors:
Legler, TJ
Eber, SW
Lakomek, M
Lynen, R
Maas, JH
Pekrun, A
Repas-Humpe, M
Schroter, W
Kohler, M
Citation: Tj. Legler et al., Application of RHD and RHCE genotyping for correct blood group determination in chronically transfused patients, TRANSFUSION, 39(8), 1999, pp. 852-855
Authors:
Siethoff, H
Ahlborn, K
Schroter, W
Citation: H. Siethoff et al., New analysis of the yield point of germanium, PHYS ST S-A, 174(1), 1999, pp. 205-212
Authors:
Figielski, T
Schroter, W
Wosinski, T
Citation: T. Figielski et al., Proceedings - Extended defects in semiconductors (EDS'98) - Preface, PHYS ST S-A, 171(1), 1999, pp. 3-3
Authors:
Seibt, M
Hedemann, H
Istratov, AA
Riedel, F
Sattler, A
Schroter, W
Citation: M. Seibt et al., Structural and electrical properties of metal silicide precipitates in silicon, PHYS ST S-A, 171(1), 1999, pp. 301-310
Authors:
Schroter, W
Citation: W. Schroter, French jurisprudence and German jurisprudence, 1870-1918, ETUD GER, 54(2), 1999, pp. 346-347
Authors:
Kugler, W
Laspe, P
Stahl, M
Schroter, W
Lakomek, M
Citation: W. Kugler et al., Identification of a novel promoter mutation in the human pyruvate kinase (PK) LR gene of a patient with severe haemolytic anaemia, BR J HAEM, 105(3), 1999, pp. 596-598
Authors:
Siethoff, H
Brion, HG
Schroter, W
Citation: H. Siethoff et al., A regime of the yield point of silicon at high temperatures, APPL PHYS L, 75(9), 1999, pp. 1234-1236
Authors:
Kugler, W
Breme, K
Laspe, P
Muirhead, H
Davies, C
Winkler, H
Schroter, W
Lakomek, M
Citation: W. Kugler et al., Molecular basis of neurological dysfunction coupled with haemolytic anaemia in human glucose-6-phosphate isomerase (GPI) deficiency, HUM GENET, 103(4), 1998, pp. 450-454
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