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Results: 1-13 |
Results: 13
Lethal pneumococcal infection in an 18-month-old girl with splenic hypoplasia and dysgammaglobulinemia
Authors: Nanan, R Peters, K Schrod, L Kreth, HW
Citation: R. Nanan et al., Lethal pneumococcal infection in an 18-month-old girl with splenic hypoplasia and dysgammaglobulinemia, ANN HEMATOL, 80(11), 2001, pp. 674-676
Periodic fever (TRAPS) caused by mutations in the TNF alpha receptor 1 (TNFRSF1A) gene of three German patients
Authors: Rosen-Wolff, A Kreth, HW Hofmann, S Hohne, K Heubner, G Mobius, D Zintl, F Gahr, M Roesler, J
Citation: A. Rosen-wolff et al., Periodic fever (TRAPS) caused by mutations in the TNF alpha receptor 1 (TNFRSF1A) gene of three German patients, EUR J HAEMA, 67(2), 2001, pp. 105-109
Homozygous and compound-heterozygous type I plasminogen deficiency is a common cause of ligneous conjunctivitis
Authors: Schuster, V Zeitler, P Seregard, S Ozcelik, U Anadol, D Luchtman-Jones, L Meire, F Mingers, AM Schambeck, C Kreth, HW
Citation: V. Schuster et al., Homozygous and compound-heterozygous type I plasminogen deficiency is a common cause of ligneous conjunctivitis, THROMB HAEM, 85(6), 2001, pp. 1004-1010
Acute and long-term effects of booster immunisation on frequencies of antigen-specific memory B-lymphocytes
Authors: Nanan, R Heinrich, D Frosch, M Kreth, HW
Citation: R. Nanan et al., Acute and long-term effects of booster immunisation on frequencies of antigen-specific memory B-lymphocytes, VACCINE, 20(3-4), 2001, pp. 498-504
X-linked lymphoproliferative disease is caused by deficiency of a novel SH2 domain-containing signal transduction adaptor protein
Authors: Schuster, V Kreth, HW
Citation: V. Schuster et Hw. Kreth, X-linked lymphoproliferative disease is caused by deficiency of a novel SH2 domain-containing signal transduction adaptor protein, IMMUNOL REV, 178, 2000, pp. 21-28
A novel sensitive approach for frequency analysis of measles virus-specific memory T-lymphocytes in healthy adults with a childhood history of natural measles
Authors: Nanan, R Rauch, A Kampgen, E Niewiesk, S Kreth, HW
Citation: R. Nanan et al., A novel sensitive approach for frequency analysis of measles virus-specific memory T-lymphocytes in healthy adults with a childhood history of natural measles, J GEN VIROL, 81, 2000, pp. 1313-1319
Measles virus infection causes transient depletion of activated T cells from peripheral circulation
Authors: Nanan, R Chittka, B Hadam, M Kreth, HW
Citation: R. Nanan et al., Measles virus infection causes transient depletion of activated T cells from peripheral circulation, J CLIN VIRO, 12(3), 1999, pp. 201-210
Human homozygous type I plasminogen deficiency and ligneous conjunctivitis
Authors: Mingers, AM Philapitsch, A Zeitler, P Schuster, V Schwarz, HP Kreth, HW
Citation: Am. Mingers et al., Human homozygous type I plasminogen deficiency and ligneous conjunctivitis, APMIS, 107(1), 1999, pp. 62-72
Combination of von Willebrand disease type 1 and partial factor XII deficiency in children: clinical evidence for a diminished bleeding tendency
Authors: Zeitler, P Meissner, N Kreth, HW
Citation: P. Zeitler et al., Combination of von Willebrand disease type 1 and partial factor XII deficiency in children: clinical evidence for a diminished bleeding tendency, ACT PAEDIAT, 88(11), 1999, pp. 1233-1237
Uncommon missense and splice mutations and resulting biochemical phenotypes in German patients with X-linked chronic granulomatous disease
Authors: Roesler, J Heyden, S Burdelski, M Schafer, H Kreth, HW Lehmann, R Paul, D Marzahn, J Gahr, M Rosen-Wolff, A
Citation: J. Roesler et al., Uncommon missense and splice mutations and resulting biochemical phenotypes in German patients with X-linked chronic granulomatous disease, EXP HEMATOL, 27(3), 1999, pp. 505-511
Reversible monoclonal lymphadenopathy in autoimmune lymphoproliferative syndrome with functional FAS (CD95/APO-1) deficiency
Authors: Strobel, P Nanan, R Gattenlohner, S Muller-Deubert, S Muller-Hermelink, HK Kreth, HW Marx, A
Citation: P. Strobel et al., Reversible monoclonal lymphadenopathy in autoimmune lymphoproliferative syndrome with functional FAS (CD95/APO-1) deficiency, AM J SURG P, 23(7), 1999, pp. 829-837
Compound-heterozygous mutations in the plasminogen gene predispose to the development of ligneous conjunctivitis
Authors: Schuster, V Seidenspinner, S Zeitler, P Escher, C Pleyer, U Bernauer, W Stiehm, ER Isenberg, S Seregard, S Olsson, T Mingers, AM Schambeck, C Kreth, HW
Citation: V. Schuster et al., Compound-heterozygous mutations in the plasminogen gene predispose to the development of ligneous conjunctivitis, BLOOD, 93(10), 1999, pp. 3457-3466
Polymorphonuclear elastase in patients with homozygous type I plasminogen deficiency and ligneous conjunctivitis
Authors: Mingers, AM Philapitsch, A Schwarz, HP Zeitler, P Kreth, HW
Citation: Am. Mingers et al., Polymorphonuclear elastase in patients with homozygous type I plasminogen deficiency and ligneous conjunctivitis, SEM THROMB, 24(6), 1998, pp. 605-612
Risultati: 1-13 |