Prof.Dr. ID: 63353

Reinhard Schneppenheim

graph of relations

Publications

  1. 1998
  2. Ins405AsnPro mutation in the von Willebrand factor propeptide in recessive type 2A (IIC) von Willebrand's disease

    Holmberg, L., Karpman, D., Isaksson, C., Kristoffersson, A. C., Lethagen, S. & Schneppenheim, R., 01.04.1998, In: THROMB HAEMOSTASIS. 79, 4, p. 718-22 5 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

  3. Bilateral renal vein thrombosis and venous sinus thrombosis in a neonate with factor V mutation (FV Leiden)

    Pohl, M., Zimmerhackl, L. B., Heinen, F., Sutor, A. H., Schneppenheim, R. & Brandis, M., 01.01.1998, In: J PEDIATR-US. 132, 1, p. 159-61 3 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

  4. 1997
  5. Arginine506 to glutamin mutation in the factor V gene in infancy and childhood: evidence of fibrinolytic impairment

    Nowak-Göttl, U., Vielhaber, H., Grohmann, J., Schneppenheim, R. & Koch, H. G., 01.03.1997, In: EUR J PEDIATR. 156, 3, p. 195-8 4 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

  6. APC resistance in childhood thromboembolism: diagnosis and clinical aspects

    Nowak-Göttl, U., Schneppenheim, R. & Vielhaber, H., 01.01.1997, In: SEMIN THROMB HEMOST. 23, 3, p. 253-8 6 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

  7. 1996
  8. Prevalence of factor V Leiden in children with thrombo-embolism

    Aschka, I., Aumann, V., Bergmann, F., Budde, U., Eberl, W., Eckhof-Donovan, S., Krey, S., Nowak-Göttl, U., Schobess, R., Sutor, A. H., Wendisch, J. & Schneppenheim, R., 01.12.1996, In: EUR J PEDIATR. 155, 12, p. 1009-14 6 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

  9. Inherited defects of the protein C anticoagulant system in childhood thrombo-embolism

    Nowak-Göttl, U., Auberger, K., Göbel, U., Kreuz, W., Schneppenheim, R., Vielhaber, H., Zenz, W. & Zieger, B., 01.11.1996, In: EUR J PEDIATR. 155, 11, p. 921-7 7 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

  10. Results of a screening for von Willebrand disease type 2N in patients with suspected haemophilia A or von Willebrand disease type 1

    Schneppenheim, R., Budde, U., Krey, S., Drewke, E., Bergmann, F., Lechler, E., Oldenburg, J. & Schwaab, R., 01.10.1996, In: THROMB HAEMOSTASIS. 76, 4, p. 598-602 5 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

  11. Von Willebrand disease

    Schneppenheim, R., 09.1996, In: EUR J PEDIATR. 155, 9, p. 751-2 2 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

  12. Hepatopathie bei Patienten mit Neuroblastom Stadium 4S

    Claviez, A., Hero, B., Schneppenheim, R. & Berthold, F., 01.07.1996, In: KLIN PADIATR. 208, 4, p. 221-8 8 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

  13. Geographic distribution and origin of CFTR mutations in Germany

    Tümmler, B., Storrs, T., Dziadek, V., Dörk, T., Meitinger, T., Golla, A., Bertele-Harms, R. M., Harms, H. K., Schröder, E., Claass, A., Rutjes, J., Schneppenheim, R., Bauer, I., Breuel, K., Stuhrmann, M., Schmidtke, J., Lindner, M., Eigel, A., Horst, J., Kaiser, R., Lentze, M. J., Schmidt, K., von der Hardt, H. & Estivill, X., 01.06.1996, In: HUM GENET. 97, 6, p. 727-31 5 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

  14. Defective dimerization of von Willebrand factor subunits due to a Cys-> Arg mutation in type IID von Willebrand disease

    Schneppenheim, R., Brassard, J., Krey, S., Budde, U., Kunicki, T. J., Holmberg, L., Ware, J. & Ruggeri, Z. M., 16.04.1996, In: P NATL ACAD SCI USA. 93, 8, p. 3581-6 6 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

  15. APC resistance in neonates and infants: adjustment of the APTT-based method

    Nowak-Göttl, U., Kohlhase, B., Vielhaber, H., Aschka, I., Schneppenheim, R. & Jürgens, H., 15.03.1996, In: THROMB RES. 81, 6, p. 665-70 6 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

  16. Resistance to activated protein C (APCR) in children with venous or arterial thromboembolism

    Nowak-Göttl, U., Koch, H. G., Aschka, I., Kohlhase, B., Vielhaber, H., Kurlemann, G., Oleszcuk-Raschke, K., Kehl, H. G., Jürgens, H. & Schneppenheim, R., 03.1996, In: BRIT J HAEMATOL. 92, 4, p. 992-8 7 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

  17. 1995
  18. First case of disseminated Mycobacterium avium infection following chemotherapy for childhood acute myeloid leukemia

    Claass, A., Claviez, A., Westphal, E., Rüsch-Gerdes, S. & Schneppenheim, R., 01.09.1995, In: INFECTION. 23, 5, p. 301-2 2 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

  19. Identification of a candidate missense mutation in a family with von Willebrand disease type IIC

    Schneppenheim, R., Thomas, K. B., Krey, S., Budde, U., Jessat, U., Sutor, A. H. & Zieger, B., 01.06.1995, In: HUM GENET. 95, 6, p. 681-6 6 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

  20. Von Willebrand disease in childhood

    Schneppenheim, R., Thomas, K. B. & Sutor, A. H., 01.01.1995, In: SEMIN THROMB HEMOST. 21, 3, p. 261-75 15 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

  21. 1994
  22. Genetic heterogeneity of severe von Willebrand disease type III in the German population

    Schneppenheim, R., Krey, S., Bergmann, F., Bock, D., Budde, U., Lange, M., Linde, R., Mittler, U., Meili, E. & Mertes, G., 01.12.1994, In: HUM GENET. 94, 6, p. 640-52 13 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

  23. The impact of EBV, proliferation rate, and Bcl-2 expression in Hodgkin's disease in childhood

    Claviez, A., Tiemann, M., Peters, J., Kreipe, H., Schneppenheim, R. & Parwaresch, R., 01.02.1994, In: ANN HEMATOL. 68, 2, p. 61-6 6 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

  24. 1993
  25. von Willebrand factor mutation enhancing interaction with platelets in patients with normal multimeric structure

    Holmberg, L., Dent, J. A., Schneppenheim, R., Budde, U., Ware, J. & Ruggeri, Z. M., 01.05.1993, In: J CLIN INVEST. 91, 5, p. 2169-77 9 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

  26. 1991
  27. Discrepant results of different tests for antibodies to hepatitis C in children with malignant diseases and in patients on renal replacement therapy

    Rautenberg, P., Schneppenheim, R., Leimenstoll, G., Behnke, H. & Loose, G., 01.11.1991, In: EUR J CLIN MICROBIOL. 10, 11, p. 978-81 4 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

  28. Seroprevalence and significance of antibodies to hepatitis C virus in pediatric patients with malignant diseases

    Schneppenheim, R., Rautenberg, P., Behnke, H. & Vietor, K., 01.07.1991, In: KLIN PADIATR. 203, 4, p. 273-5 3 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

  29. Luminography--a new, highly sensitive visualization method for electrophoresis

    Schneppenheim, R., Budde, U., Dahlmann, N. & Rautenberg, P., 01.05.1991, In: ELECTROPHORESIS. 12, 5, p. 367-72 6 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

  30. 1990
  31. Luminographic detection of von Willebrand factor multimers in agarose gels and on nitrocellulose membranes

    Budde, U., Schneppenheim, R., Plendl, H., Dent, J., Ruggeri, Z. M. & Zimmerman, T. S., 12.04.1990, In: THROMB HAEMOSTASIS. 63, 2, p. 312-5 4 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

  32. 1989
  33. An EcoRI polymorphism in the human von Willebrand factor (vWF) gene

    Ewerhardt, B., Ludwig, M., Schwaab, R., Schneppenheim, R. & Olek, K., 11.07.1989, In: NUCLEIC ACIDS RES. 17, 13, p. 5416

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

  34. 1988
  35. Luminography--an alternative assay for detection of von Willebrand factor multimers

    Schneppenheim, R., Plendl, H. & Budde, U., 31.10.1988, In: THROMB HAEMOSTASIS. 60, 2, p. 133-6 4 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

  36. 1987
  37. A luminescence Western blot with enhanced sensitivity for antibodies to human immunodeficiency virus

    Schneppenheim, R. & Rautenberg, P., 01.02.1987, In: EUR J CLIN MICROBIOL. 6, 1, p. 49-51 3 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

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