M Kraemer

Summary

Country: Germany

Publications

  1. ncbi request reprint Mrnp41 (Rae 1p) associates with microtubules in HeLa cells and in neurons
    D Kraemer
    Medizinische Poliklinik, Julius Maximilians Universitat, Wurzburg, Germany
    Eur J Cell Biol 80:733-40. 2001
  2. ncbi request reprint Splenectomy in patients with mixed myelodysplastic/myeloproliferative disease
    D Kraemer
    Medizinische Poliklinik, University Wurzburg, Germany
    Ann Hematol 81:308-11. 2002
  3. ncbi request reprint [Gilbert disease and type I and II Crigler-Najjar syndrome due to mutations in the same UGT1A1 gene locus]
    Doris Kraemer
    Medizinische Poliklinik, Universitat Wurzburg
    Med Klin (Munich) 97:528-32. 2002
  4. ncbi request reprint Aseptic necrosis of both femoral heads as first symptom of chronic myelogenous leukemia
    M Kraemer
    Medizinische Poliklinik, University of Wuerzburg, Klinikstr 8, 97070 Wuerzburg, Germany
    Ann Hematol 82:44-6. 2003
  5. pmc Nucleoporin p62 antibodies in a case of mixed connective tissue disease
    Doris M Kraemer
    Medizinische Poliklinik, University of Wurzburg, 97070 Wurzburg, Germany
    Clin Diagn Lab Immunol 10:329-31. 2003
  6. ncbi request reprint Kidney Na+,K(+)-ATPase is associated with moesin
    Doris M Kraemer
    Medizinische Poliklinik, University of Wurzburg, Wurzburg, Germany
    Eur J Cell Biol 82:87-92. 2003
  7. ncbi request reprint Evaluation of a novel case-based training program (d3web.Train) in hematology
    Doris Kraemer
    Medizinische Poliklinik der Universitätsklinik Würzburg, Klinikstr 6 8, 97070, Wurzburg, Germany
    Ann Hematol 84:823-9. 2005
  8. ncbi request reprint Missense mutation in a patient with X-linked dyskeratosis congenita
    Doris M Kraemer
    Medizinische Poliklinik, Klinikstr 8, 97070 Wurzburg, Germany
    Haematologica 88:ECR11. 2003
  9. ncbi request reprint Heterozygous G71R-mutation causing Gilbert's syndrome in one of 103 random persons of German descent
    Marlis Sava
    J Hepatol 42:778-9. 2005

Collaborators

Detail Information

Publications9

  1. ncbi request reprint Mrnp41 (Rae 1p) associates with microtubules in HeLa cells and in neurons
    D Kraemer
    Medizinische Poliklinik, Julius Maximilians Universitat, Wurzburg, Germany
    Eur J Cell Biol 80:733-40. 2001
    ..The essential role of mrnp41 in spindle pole separation and cell cycle progression may also be related to its ability to bind to MTs...
  2. ncbi request reprint Splenectomy in patients with mixed myelodysplastic/myeloproliferative disease
    D Kraemer
    Medizinische Poliklinik, University Wurzburg, Germany
    Ann Hematol 81:308-11. 2002
    ..Additionally, we indicate the potential positive outcome of splenectomy as ultima ratio in patients with these hematological features and severe thrombopenia...
  3. ncbi request reprint [Gilbert disease and type I and II Crigler-Najjar syndrome due to mutations in the same UGT1A1 gene locus]
    Doris Kraemer
    Medizinische Poliklinik, Universitat Wurzburg
    Med Klin (Munich) 97:528-32. 2002
    ..Crigler-Najjar syndrome II leads to a more serious kind of hyperbilirubinemia. In case of Crigler-Najjar syndrome I patients are suffering from a very severe hyperbilirubinemia, which often causes death during the first months of life...
  4. ncbi request reprint Aseptic necrosis of both femoral heads as first symptom of chronic myelogenous leukemia
    M Kraemer
    Medizinische Poliklinik, University of Wuerzburg, Klinikstr 8, 97070 Wuerzburg, Germany
    Ann Hematol 82:44-6. 2003
    ..This is a very rare complication of severe leukostasis, leading to the diagnosis of CML in this case. To our knowledge, this is the first case of an adult patient showing aseptic necrosis of femoral heads caused by leukostasis...
  5. pmc Nucleoporin p62 antibodies in a case of mixed connective tissue disease
    Doris M Kraemer
    Medizinische Poliklinik, University of Wurzburg, 97070 Wurzburg, Germany
    Clin Diagn Lab Immunol 10:329-31. 2003
    ..Thus far, p62 antibodies have mainly been described in cases of primary biliary cirrhosis. We speculate that the presence of p62 antibodies is an indication of a poor prognosis in connective tissue disorders...
  6. ncbi request reprint Kidney Na+,K(+)-ATPase is associated with moesin
    Doris M Kraemer
    Medizinische Poliklinik, University of Wurzburg, Wurzburg, Germany
    Eur J Cell Biol 82:87-92. 2003
    ..1 modifying the binding of ankyrin to the cytoplasmic domain of the erythrocyte anion exchanger (AE1)...
  7. ncbi request reprint Evaluation of a novel case-based training program (d3web.Train) in hematology
    Doris Kraemer
    Medizinische Poliklinik der Universitätsklinik Würzburg, Klinikstr 6 8, 97070, Wurzburg, Germany
    Ann Hematol 84:823-9. 2005
    ..The d3web.Train system offers a new and great tool for creating a training program in a reasonable amount of time, because it is able to process available patient records...
  8. ncbi request reprint Missense mutation in a patient with X-linked dyskeratosis congenita
    Doris M Kraemer
    Medizinische Poliklinik, Klinikstr 8, 97070 Wurzburg, Germany
    Haematologica 88:ECR11. 2003
    ..This is the third description of a mutation in codon 350 (exon 11), changing a very well conserved amino acid in the pseudouridine synthase (PUA) domain of dyskerin...
  9. ncbi request reprint Heterozygous G71R-mutation causing Gilbert's syndrome in one of 103 random persons of German descent
    Marlis Sava
    J Hepatol 42:778-9. 2005