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La ricerca find articoli where authors phrase all words ' Pekrun, A' sort by level,fasc_key/DESCEND, pagina_ini_num/ASCEND ha restituito 42 riferimenti
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    1. Reinhardt, D; Witt, O; Miosge, N; Herken, R; Pekrun, A
      Increase in band 3 density and aggregation in hereditary spherocytosis

      BLOOD CELLS MOLECULES AND DISEASES
    2. Reinhardt, D; Witt, O; Miosge, N; Herken, R; Pekrun, A
      Increase in band 3 density and aggregation in hereditary spherocytosis

      BLOOD CELLS MOLECULES AND DISEASES
    3. Erdlenbruch, B; Pekrun, A; Roth, C; Grunewald, RW; Kern, W; Lakomek, M
      Cisplatin nephrotoxicity in children after continuous 72-h and 3x1-h infusions

      PEDIATRIC NEPHROLOGY
    4. Reinhardt, D; Ridder, R; Kugler, W; Pekrun, A
      Post-transcriptional effects of interleukin-3, interferon-gamma, erythropoietin and butyrate on in vitro hemoglobin chain synthesis in congenital hemolytic anemia

      HAEMATOLOGICA
    5. Witt, O; Schulze, S; Kanbach, K; Roth, C; Pekrun, A
      Tumor cell differentiation by butyrate and environmental stress

      CANCER LETTERS
    6. Papos, M; Pekrun, A; Herms, JW; Behr, TM; Meller, J; Rustenbeck, HH; Kretzschmar, HA; Becker, W
      Somatostatin receptor scintigraphy in the management of cerebral malignantectomesenchymoma: a case report

      PEDIATRIC RADIOLOGY
    7. Erdlenbruch, B; Nier, M; Kern, W; Hiddemann, W; Pekrun, A; Lakomek, M
      Pharmacokinetics of cisplatin and relation to nephrotoxicity in paediatricpatients

      EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY
    8. Witt, O; Schmejkal, S; Pekrun, A
      Tributyrin plus all-trans-retinoic acid efficiently induces fetal hemoglobin expression in human erythroleukemia cells

      AMERICAN JOURNAL OF HEMATOLOGY
    9. Reinhardt, D; Behnke-Mursch, J; Weiss, E; Christen, HJ; Kuhl, J; Lakomek, M; Pekrun, A
      Rhabdoid tumors of the central nervous system

      CHILDS NERVOUS SYSTEM
    10. Roth, C; Bokemeier, M; Bartz, M; Leonhardt, U; Erdlenbruch, B; Schroter, W; Pekrun, A
      Glucose tolerance disorders in patients suffering from thalassemia major

      MONATSSCHRIFT KINDERHEILKUNDE
    11. Reinhardt, D; Pekrun, A; Lakomek, M; Zimmermann, M; Ritter, J; Creutzig, U
      Primary myelosarcomas are associated with a high rate of relapse: report on 34 children from the acute myeloid leukaemia-Berlin-Frankfurt-Munster studies

      BRITISH JOURNAL OF HAEMATOLOGY
    12. Witt, O; Sand, K; Pekrun, A
      Butyrate-induced erythroid differentiation of human K562 leukemia cells involves inhibition of ERK and activation of p38 MAP kinase pathways

      BLOOD
    13. Iglauer, A; Reinhardt, D; Schroter, W; Pekrun, A
      Cryohemolysis test as a diagnostic tool for hereditary spherocytosis

      ANNALS OF HEMATOLOGY
    14. Reinhardt, D; Pekrun, A; Lakomek, M; Ritter, J; Creutzig, U
      Primary isolated myelosarcoma in childhood

      KLINISCHE PADIATRIE
    15. Legler, TJ; Eber, SW; Lakomek, M; Lynen, R; Maas, JH; Pekrun, A; Repas-Humpe, M; Schroter, W; Kohler, M
      Application of RHD and RHCE genotyping for correct blood group determination in chronically transfused patients

      TRANSFUSION
    16. Reinhardt, D; Pekrun, A; Lakomek, M; Ritter, J; Creutzig, U
      Isolated myelosarcoma of the skin in childhood

      MONATSSCHRIFT KINDERHEILKUNDE
    17. Kohn, B; Freistedt, R; Pekrun, A; Wang, P; Giger, U
      Erythrocyte pyruvate kinase deficiency causing chronic hemolytic anemia and osteosclerosis in a longhaired dachshund

      KLEINTIERPRAXIS
    18. REINHARDT D; HAASE D; SCHOCH C; WOLLENWEBER S; HINKELMAN E; VONHEYDEN W; LENTINI G; WORMANN B; SCHROTER W; PEKRUN A
      HEMOGLOBIN-F IN MYELODYSPLASTIC SYNDROME

      Annals of hematology
    19. WEISS E; BEHRING B; BEHNKE J; CHRISTEN HJ; PEKRUN A; HESS CF
      TREATMENT OF PRIMARY MALIGNANT RHABDOID TUMOR OF THE BRAIN - REPORT OF 3 CASES AND REVIEW OF THE LITERATURE

      International journal of radiation oncology, biology, physics
    20. WIETHOFF L; CHRISTEN HJ; PEKRUN A; MURSCH K; KOCH G; DOKER B; ANDLER W
      CLINICAL SYMPTOMS OF INTRACRANIAL GERM-CELL TUMORS

      Monatsschrift fur Kinderheilkunde
    21. HUPPKE P; WUNSCH D; PEKRUN A; KIND H; WINKLER H; SCHROTER W; LAKOMEK M
      GLUCOSE PHOSPHATE ISOMERASE DEFICIENCY - BIOCHEMICAL AND MOLECULAR-GENETIC STUDIES ON THE ENZYME VARIANTS OF 2 PATIENTS WITH SEVERE HEMOLYTIC-ANEMIA

      European journal of pediatrics
    22. ROTH C; PEKRUN A; BARTZ M; JARRY H; EBER S; LAKOMEK M; SCHROTER W
      SHORT STATURE AND FAILURE OF PUBERTAL DEVELOPMENT IN THALASSEMIA MAJOR - EVIDENCE FOR HYPOTHALAMIC NEUROSECRETORY DYSFUNCTION OF GROWTH-HORMONE SECRETION AND DEFECTIVE PITUITARY GONADOTROPIN-SECRETION

      European journal of pediatrics
    23. EBER SW; GONZALEZ JM; LUX ML; SCARPA AL; TSE WT; DORNWELL M; HERBERS J; KUGLER W; OZCAN R; PEKRUN A; GALLAGHER PG; SCHROTER W; FORGET BG; LUX SE
      ANKYRIN-1 MUTATIONS ARE A MAJOR CAUSE OF DOMINANT AND RECESSIVE HEREDITARY SPHEROCYTOSIS

      Nature genetics
    24. KREUDER J; BORKHARDT A; REPP R; PEKRUN A; GOTTSCHE B; GOTTSCHALK U; REICHMANN H; SCHACHENMAYR W; SCHLEGEL K; LAMPERT F
      BRIEF REPORT - INHERITED METABOLIC MYOPATHY AND HEMOLYSIS DUE TO A MUTATION IN ALDOLASE-A

      The New England journal of medicine
    25. PEKRUN A; FLECKSTEIN W; SCHROTER W
      SUCCESSFUL THERAPY IN HOMOZYGOUS BETA-THA LASSEMIA BY A METICULOUS TRANSFUSION REGIMEN AND DEFEROXAMINE

      Monatsschrift fur Kinderheilkunde
    26. EBER SW; GROSCHE M; DITZIG M; PEKRUN A; LAKOMEK M; SCHROTER W
      COMPLICATIONS FOLLOWING SPLENECTOMY IN BE NIGN HEMATOLOGICAL DISEASE IN CHILDREN AND ADOLESCENTS

      Monatsschrift fur Kinderheilkunde
    27. ZOELLER G; PEKRUN A; RINGERT RH; LAKOMEK M
      STAGING PROBLEMS IN THE PREOPERATIVE CHEMOTHERAPY OF WILMS-TUMOR - REPLY

      British Journal of Urology
    28. ZOLLER G; KUNZE E; PEKRUN A; RINGERT RH
      RENAL-CELL CARCINOMA IN CHILDREN - A RARE DIFFERENTIAL-DIAGNOSIS OF WILMS-TUMOR

      Pediatric surgery international
    29. PEKRUN A; NEUBAUER BA; EBER SW; LAKOMEK M; SEIDEL H; SCHROTER W
      TRIOSEPHOSPHATE ISOMERASE DEFICIENCY - BIOCHEMICAL AND MOLECULAR-GENETIC ANALYSIS FOR PRENATAL-DIAGNOSIS

      Clinical genetics
    30. ZOELLER G; PEKRUN A; LAKOMEK M; RINGERT RH
      STAGING PROBLEMS IN THE PREOPERATIVE CHEMOTHERAPY OF WILMS-TUMOR

      British Journal of Urology
    31. HAASE D; FEURINGBUSKE M; KONEMANN S; FONATSCH C; TROFF C; VERBEEK W; PEKRUN A; HIDDEMANN W; WORMANN B
      EVIDENCE FOR MALIGNANT TRANSFORMATION IN ACUTE MYELOID-LEUKEMIA AT THE LEVEL OF EARLY HEMATOPOIETIC STEM-CELLS BY CYTOGENETIC ANALYSIS OF CD34(+) SUBPOPULATIONS

      Blood
    32. PINDER JC; PEKRUN A; MAGGS AM; BRAIN APR; GRATZER WB
      ASSOCIATION STATE OF HUMAN RED-BLOOD-CELL BAND-3 AND ITS INTERACTION WITH ANKYRIN

      Blood
    33. PEKRUN A; LAKOMEK M; EBER S; KONRAD H; SCHROTER W
      DIAGNOSIS OF PYRUVATE-KINASE DEFICIENCY I N THE PRESENCE OF A HIGH RETICULOCYTE COUNT

      Deutsche Medizinische Wochenschrift
    34. LAKOMEK M; WINKLER H; PEKRUN A; KRUGER N; SANDER M; HUPPKE P; SCHROTER W
      ERYTHROCYTE PYRUVATE-KINASE DEFICIENCY - THE INFLUENCE OF PHYSIOLOGICALLY IMPORTANT METABOLITES ON THE FUNCTION OF NORMAL AND DEFECTIVE ENZYMES

      Enzyme & protein
    35. LAKOMEK M; HUPPKE P; NEUBAUER B; PEKRUN A; WINKLER H; SCHROTER W
      MUTATIONS IN THE R-TYPE PYRUVATE-KINASE GENE AND ALTERED ENZYME-KINETIC PROPERTIES IN PATIENTS WITH HEMOLYTIC-ANEMIA DUE TO PYRUVATE-KINASEDEFICIENCY

      Annals of hematology
    36. PEKRUN A; SCHIFMANN H; LAKOMEK M
      LYSIS OF CHEMOTHERAPY-ASSOCIATED THROMBOS IS OF THE VENA-AXILLARIS

      Klinische Padiatrie
    37. ZOELLER G; PEKRUN A; LAKOMEK M; RINGERT RH
      WILMS-TUMOR - THE PROBLEM OF DIAGNOSTIC-ACCURACY IN CHILDREN UNDERGOING PREOPERATIVE CHEMOTHERAPY WITHOUT HISTOLOGICAL TUMOR VERIFICATION

      The Journal of urology
    38. EBER SW; PEKRUN A; REINHARDT D; SCHROTER W; LUX SE
      HEREDITARY SPHEROCYTOSIS WITH ANKYRIN WALSRODE, A VARIANT ANKYRIN WITH DECREASED AFFINITY FOR BAND-3

      Blood
    39. PEKRUN A; EBER SW; KUHLMEY A; SCHROTER W
      COMBINED ANKYRIN AND SPECTRIN DEFICIENCY IN HEREDITARY SPHEROCYTOSIS

      Annals of hematology
    40. EBER SW; CHO M; BRUGNARA C; MOHANDAS N; GOLAN DE; PEKRUN A; DORNWELL M; HANSPAL M; LIU SC; CHILCOTE R; PALEK J; FORGET BG; LUX SE
      INCREASED BAND 3 MOBILITY AND DECREASED ANION TRANSPORT IN ANKYRIN DEFICIENT HEREDITARY SPHEROCYTES

      Blood
    41. EBER SW; LUX ML; GONZALEZ JM; SCARPA A; TSE WT; GALLAGHER PG; PEKRUN A; FORGET BG; LUX SE
      DISCOVERY OF 8 ANKYRIN MUTATIONS IN HEREDITARY SPHEROCYTOSIS (HS) INDICATES THAT ANKYRIN DEFECTS ARE A MAJOR CAUSE OF DOMINANT AND RECESSIVE HS

      Blood
    42. PEKRUN A; LAKOMEK M; ENG W; SCHROTER W
      PYRIMIDINE-5'-NUCLEOTIDASE DEFICIENCY AS A CONGENITAL CAUSE OF NONSPHEROCYTIC HEMOLYTIC-ANEMIA

      Deutsche Medizinische Wochenschrift


ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 29/05/20 alle ore 19:56:18