Department of Pediatric Hematology and Oncology

Publications

  1. Dissertations › Research
  2. Conference contribution - Article for conference › Research › Not peer-reviewed
  3. Glioblastoma in childhood – Treatment and outcome of 7 patients

    Burkhardt, T., Emami, P., Kordes, U., Matschke, J., Regelsberger, J., Westphal, M. & Kammler, G., 01.04.2011, 62. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC) Joint Meeting mit der Polnischen Gesellschaft für Neurochirurgen (PNCH).

    Research output: SCORING: Contribution to book/anthologyConference contribution - Article for conferenceResearch

  4. SIOP-CPT-2000 update

    Kordes, U., Kutluk, T., Hasselblatt, M., Pietsch, A. M. T., Thall, P. & Wolff, J. E., 2011, 62. Jahrestagung der Deutschen Gesellschaft für Neurochirurgie (DGNC) Joint Meeting mit der Polnischen Gesellschaft für Neurochirurgen (PNCH).

    Research output: SCORING: Contribution to book/anthologyConference contribution - Article for conferenceResearch

  5. Conference contribution - Published abstract for conference with selection process › Research › Peer-reviewed
  6. Risikofaktoren für einen gemischten Chimerismus nach Stammzelltransplantation mit Treosulfan- oder Melphalanbasierter Konditionierung bei Kindern und Jugendlichen mit primärer Hämophagozytischer Lymphohistiozytose

    Wustrau, K., Albert, M. H., Bader, P., Beier, R., Burkhardt, B., Chada, M., Greil, J., Gruhn, B., Kühl, J-S., Lang, P., Meisel, R., Schulz, A., Seidel, M., Speckmann, C., Sykora, K-W., Wawer, A., Wößmann, W., Ozga, A-K., Janka-Schaub, G., Ehl, S., Müller, I. & Lehmberg, K., 2019, Monatsschrift Kinderheilkunde > Ausgabe 7/2018 : Abstracts der 91. Wissenschaftlichen Halbjahrestagung der Gesellschaft für Pädiatrische Onkologie und Hämatologie (GPOH). Vol. 01.07.2018 | Abstracts | Ausgabe 7/2018 . p. 646-647

    Research output: SCORING: Contribution to book/anthologyConference contribution - Published abstract for conference with selection processResearchpeer-review

  7. Risk factors for mixed chimerism after stem cell transplantation with treosulfan or melphalan based conditioning regimens in children and adolescents with primary hemophagocytic lymphohistocytosis

    Wustrau, K., Albert, M. H., Bader, P., Beier, R., Burkhardt, B., Chada, M., Greil, J., Gruhn, B., Kühl, J-S., Lang, P., Meisel, R., Schulz, A., Seidel, M., Speckmann, C., Sykora, K-W., Wawer, A., Wößmann, W., Ozga, A-K., Ehl, S., Müller, I. & Lehmberg, K., 24.09.2018, Bone Marrow Transplantation (2018) Abstracts Collection: The 44th Annual Meeting of the European Society for Blood and Marrow Transplantation:Physicians Oral Session.

    Research output: SCORING: Contribution to book/anthologyConference contribution - Published abstract for conference with selection processResearchpeer-review

  8. Conference contribution - Poster › Research
  9. Neuroimaging findings in children with hereditary hemophagocytic lymphohistiocytosis – report from the German reference center

    Löbel, U., Wustrau, K., Müller, I., Janka-Schaub, G., Fiehler, J. & Lehmberg, K., 03.10.2018, NeuroRAD 2018 - 53. Jahrestagung der Deutschen Gesellschaft für Neuroradiologe e.V..

    Research output: SCORING: Contribution to book/anthologyConference contribution - PosterResearch

  10. SCORING: Contribution to collected editions/anthologies › Research › Peer-reviewed
  11. Hämophagozytische Lymphohistiozytose

    Lehmberg, K., 2018, Referenz Hämatologie. Kreuzer, K-A. (ed.). Georg Thieme Verlag KG

    Research output: SCORING: Contribution to book/anthologySCORING: Contribution to collected editions/anthologiesResearchpeer-review

  12. Histiozytäre Erkrankungen

    Lehmberg, K., 2018, Pädiatrische Hämatologie und Onkologie. Niemeyer, C. & Eggert, A. (eds.). 2 ed. Springer, (Springer Reference Medizin).

    Research output: SCORING: Contribution to book/anthologySCORING: Contribution to collected editions/anthologiesResearchpeer-review

  13. Neuroonkologie

    Kammler, G., Kordes, U., Hornung, D., LINHART, D. & Hagel, C., 2009, Neuropädiatrie - Evidenzbasierte Therapie. Elsevier, p. 215-239 25 p.

    Research output: SCORING: Contribution to book/anthologySCORING: Contribution to collected editions/anthologiesResearchpeer-review

  14. SCORING: Contribution to collected editions/anthologies › Education › Not peer-reviewed
  15. Infantile malignant brain tumors

    von Hoff, K. & Rutkowski, S. J., 2013, Tumors of the pediatric central nervous system. Keating, R. F., Tait Goodrich, J. & Packer, R. J. (eds.). 2. ed. New York: Georg Thieme Verlag KG

    Research output: SCORING: Contribution to book/anthologySCORING: Contribution to collected editions/anthologiesEducation

  16. Minimal Disseminated and Minimal Residual Disease in Pediatric Non-Hodgkin Lymphoma

    Mussolin, L., Damm-Welk, C. & Wößmann, W., 2019, Non-Hodgkin´s Lymphoma in Children and Adolescence. Abla, O. & Attarbaschi, A. (eds.). 1 ed. Cham: Springer, p. 119 - 129 11 p.

    Research output: SCORING: Contribution to book/anthologySCORING: Contribution to collected editions/anthologiesEducation

  17. SCORING: Contribution to collected editions/anthologies › Education › Peer-reviewed
  18. Diagnostics and Diagnosis of Late Effects in Childhood Brain Tumour Survivors

    Tallen, G., Mynarek, M., Tischler, T., Weller, M. & Rutkowski, S. J., 2021, Late Treatment Effects and Cancer Survivor Care in the Young: From Childhood to Early Adulthood. Beck, J. D., Bokemeyer, C. & Langer, T. (eds.). 1 ed. Cham: Springer Nature Switzerland, p. 239-251 13 p.

    Research output: SCORING: Contribution to book/anthologySCORING: Contribution to collected editions/anthologiesEducationpeer-review

  19. Neuroonkologie

    Rutkowski, S. J., Hornung, D., Kordes, U., Kammler, G., Hagel, C., Löbel, U., Ebinger, M., Rössler, J., Resch, A. & Linhart, D., 2014, Neuropädiatrie - Evidenzbasierte Therapie. Korinthenberg, R., Panteliadis, C. P. & Hagel, C. (eds.). 2 ed. München: Elsevier, 27 p. 12

    Research output: SCORING: Contribution to book/anthologySCORING: Contribution to collected editions/anthologiesEducationpeer-review

  20. SCORING: Contribution to collected editions/anthologies › Transfer › Not peer-reviewed
  21. Klinische Praxis - Spenderfindung und Stammzelltransplantation

    Müller, I., 2015, Rettende Geschwister: Ethische Aspekte der Einwilligung in der pädiatrischen Stammzelltransplantation. Schües, C. & Rehmann-Sutter, C. (eds.). 2015 ed. Münster: Mentis, p. 25 - 32 8 p. 2

    Research output: SCORING: Contribution to book/anthologySCORING: Contribution to collected editions/anthologiesTransfer

  22. SCORING: Journal article › Research › Not peer-reviewed
  23. CPT SIOP

    Wolff, J., Hasselblatt, M., Hartung, S., Powell, M., Garami, M., Traunecker, H., Thall, P., Mahajan, A., Kordes, U. & Sumerauer, D., 2012, In: J NEURO-ONCOL. 14, p. i153

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearch

  24. Insulin-like factor 3 - where are we now?

    Ivell, R., Hartung, S. & Anand-Ivell, R., 01.05.2005, In: ANN NY ACAD SCI. 1041, p. 486-96 11 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearch

  25. The molecular basis of cryptorchidism

    Ivell, R. & Hartung, S., 01.04.2003, In: MOL HUM REPROD. 9, 4, p. 175-81 7 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearch

  26. SCORING: Journal article › Research › Peer-reviewed
  27. 10 years' neuroblastoma screening in Europe: preliminary results of a clinical and biological review from the Study Group for Evaluation of Neuroblastoma Screening in Europe (SENSE).

    Erttmann, R., Tafese, T., Berthold, F., Kerbl, R., Mann, J., Parker, L., Schilling, F., Ambros, P., Christiansen, H., Favrot, M., Kabisch, H., Hero, B. & Philip, T., 1998, In: EUR J CANCER. 34, 9, p. 1391-1397 9.

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

  28. 11 hemophilia A patients without mutations in the factor VIII encoding gene

    Klopp, N., Oldenburg, J., Uen, C., Schneppenheim, R. & Graw, J., 01.08.2002, In: THROMB HAEMOSTASIS. 88, 2, p. 357-60 4 p.

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

  29. 2016 Classification Criteria for Macrophage Activation Syndrome Complicating Systemic Juvenile Idiopathic Arthritis: A European League Against Rheumatism/American College of Rheumatology/Paediatric Rheumatology International Trials Organisation Collaborative Initiative

    Ravelli, A., Minoia, F., Davì, S., Horne, A., Bovis, F., Pistorio, A., Aricò, M., Avcin, T., Behrens, E. M., De Benedetti, F., Filipovic, L., Grom, A. A., Henter, J-I., Ilowite, N. T., Jordan, M. B., Khubchandani, R., Kitoh, T., Lehmberg, K., Lovell, D. J., Miettunen, P., Nichols, K. E., Ozen, S., Pachlopnik Schmid, J., Ramanan, A. V., Russo, R., Schneider, R., Sterba, G., Uziel, Y., Wallace, C., Wouters, C., Wulffraat, N., Demirkaya, E., Brunner, H. I., Martini, A., Ruperto, N., Cron, R. Q. & Paediatric Rheumatology International Trials Organisation, the Childhood Arthritis and Rheumatology Research Alliance, the Pediatric Rheumatology Collaborative Study Group, and the Histiocyte Society, 03.2016, In: ANN RHEUM DIS. 75, 3, p. 481-9 9 p.

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

  30. [28-year old female patient with respiratory insufficiency, elevated liver enzymes, pancytopenia and fever].

    Wolschke, C., Fiedler, W., Habermann, C., Janka-Schaub, G. & Kluge, S., 2010, In: INTERNIST. 51, 11, p. 1434-1438 11.

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

  31. 2% Hämophilie-A-Patienten ohne Mutation im FVIII-Gen

    Uen, C., Oldenburg, J., Schröder, J., Brackmann, H-J., Schramm, W., Schwaab, R., Schneppenheim, R. & Graw, J., 01.02.2003, In: HAMOSTASEOLOGIE. 23, 1, p. 1-5 5 p.

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

  32. 68Ga-FAPI-PET/CT improves diagnostic staging and radiotherapy planning of adenoid cystic carcinomas – Imaging analysis and histological validation

    Röhrich, M., Syed, M., Liew, D. P., Giesel, F. L., Liermann, J., Choyke, P. L., Wefers, A. K., Ritz, T., Szymbara, M., Schillings, L., Heger, U., Rathke, H., Kratochwil, C., Huber, P. E., Deimling, A. V., Debus, J., Kauczor, H-U., Haberkorn, U. & Adeberg, S., 07.2021, In: RADIOTHER ONCOL. 160, p. 192-201 10 p.

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

  33. 7-Hydroxy-methotrexate and clinical toxicity following high-dose methotrexate therapy.

    Erttmann, R., Bielack, S. & Landbeck, G., 1985, In: J CANCER RES CLIN. 109, 1, p. 86-88 1.

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

  34. A 2013/2014 northern hemisphere season surface antigen inactivated trivalent influenza vaccine - Assessing the immunogenicity and safety in an open label, uncontrolled study

    Roggelin, L., Vinnemeier, C. D., Meyer, S., Witte, K., Marx, L., Theeß, W., Burchard, G. D., Rolling, T. & Cramer, J. P., 03.10.2015, In: HUM VACC IMMUNOTHER. 11, 10, p. 2370-5

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

  35. A 2-year-old boy with recurrent severe bleeding: von Willebrand type 2B and ITP--or von Willebrand type 2B alone?

    Rauch, R., Budde, U., Schneppenheim, R., Ries, M., Girisch, M. & Klinge, J., 01.12.1999, In: EUR J PEDIATR. 158 Suppl 3, p. S171-3

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

  36. A 76-year-old woman with paraplegia

    Rémi, J., Pfefferkorn, T., König, F. B., Lassmann, H., Brück, W., Holtmannspötter, M., Straube, A., Kretzschmar, H. A. & Schüller, U., 03.2010, In: BRAIN PATHOL. 20, 2, p. 507-10 4 p.

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

  37. A91V is a polymorphism in the perforin gene not causative of an FHLH phenotype.

    Udo, Z. S., Beutel, K., Weber, B., Kabisch, H., Schneppenheim, R. & Janka-Schaub, G., 2004, In: BLOOD. 104, 6, p. 1910 6.

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

  38. Aberrant ZNF423 impedes B cell differentiation and is linked to adverse outcome of ETV6-RUNX1 negative B precursor acute lymphoblastic leukemia

    Harder, L., Eschenburg, G., Zech, A., Kriebitzsch, N., Otto, B., Streichert, T., Behlich, A-S., Dierck, K., Klingler, B., Hansen, A., Stanulla, M., Zimmermann, M., Kremmer, E., Stocking, C. & Horstmann, M. A., 21.10.2013, In: J EXP MED. 210, 11, p. 2289-304 16 p.

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

  39. Absence of mutations in the AKT1 oncogene in glioblastomas and medulloblastomas

    Schüller, U., Ruiter, M., Herms, J., Kretzschmar, H. A. & Grasbon-Frodl, E., 03.2008, In: ACTA NEUROPATHOL. 115, 3, p. 367-8 2 p.

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

  40. [Abt-Letterer-Siwe disease. Diagnosis and therapy (author's transl)]

    Wolff, H. H. & Janka-Schaub, G., 1978, In: MONATSSCHR KINDERH. 126, 7, p. 425-430 7.

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

  41. A Case of a Bilateral Cicatricial Upper Eyelid Entropion After Hematopoietic Stem Cell Transplantation in Mucopolysaccharidosis Type I

    Dulz, S., Wagenfeld, L., Richard, G., Schrum, J., Muschol, N. & Keserü, M., 19.11.2015, In: OPHTHAL PLAST RECONS.

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

  42. Accessibility and quality of secondary care rheumatology services for people with inflammatory arthritis: a regional survey.

    Sandhu, R. S., Treharne, G. J., Justice, E. A., Jordan, A. C., Saravana, S., Obrenovic, K., Erb, N., Kitas, G. D. & Rowe, I. F., 2007, In: CLIN MED. 7, 6, p. 579-584 6.

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

  43. Accurate calling of KIAA1549-BRAF fusions from DNA of human brain tumours using methylation array-based copy number and gene panel sequencing data

    Stichel, D., Schrimpf, D., Sievers, P., Reinhardt, A., Suwala, A. K., Sill, M., Reuss, D. E., Korshunov, A., Casalini, B. M., Sommerkamp, A. C., Ecker, J., Selt, F., Sturm, D., Gnekow, A., Koch, A., Simon, M., Hernáiz Driever, P., Schüller, U., Capper, D., van Tilburg, C. M., Witt, O., Milde, T., Pfister, S. M., Jones, D. T. W., von Deimling, A., Sahm, F. & Wefers, A. K., 04.2021, In: NEUROPATH APPL NEURO. 47, 3, p. 406-414 9 p.

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

  44. A classification based on T cell selection-related phenotypes identifies a subgroup of childhood T-ALL with favorable outcome in the COALL studies.

    Niehues, T., Kapaun, P., Harms, D. O., Burdach, S., Kramm, C., Körholz, D., Janka-Schaub, G. & Göbel, U., 1999, In: LEUKEMIA. 13, 4, p. 614-617 4.

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

  45. A cluster of mutations in the D3 domain of von Willebrand factor correlates with a distinct subgroup of von Willebrand disease: type 2A/IIE.

    Schneppenheim, R., Michiels, J. J., Obser, T., Oyen, F., Pieconka, A., Schneppenheim, S., Will, K., Zieger, B. & Ulrich, B., 10.06.2010, In: BLOOD. 115, 23, p. 4894-4901 8 p., 23.

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

  46. A common 253-kb deletion involving VWF and TMEM16B in German and Italian patients with severe von Willebrand disease type 3.

    Schneppenheim, R., Castaman, G., Federici, A. B., Kreuz, W., Marschalek, R., Oldenburg, J., Oyen, F. & Budde, U., 2007, In: J THROMB HAEMOST. 5, 4, p. 722-728 4.

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

  47. A common origin of the 4143insA ADAMTS13 mutation.

    Schneppenheim, R., Hovinga, K., Johanna, A., Becker, T., Ulrich, B., Karpman, D., Brockhaus, W., Hrachovinová, I., Oyen, F., Oyen, F., Rittich, S., von Rosen, J., Tjønnfjord, G. E., Pimanda, J. E., Wienker, T. F. & Lämmle, B., 2006, In: THROMB HAEMOSTASIS. 96, 1, p. 3-6 1.

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

  48. A comparison between three graft manipulation methods for haploidentical stem cell transplantation in pediatric patients: preliminary results of a pilot study

    Lang, P., Schumm, M., Greil, J., Bader, P., Klingebiel, T., Müller, I., Feuchtinger, T., Pfeiffer, M., Schlegel, P-G., Niethammer, D. & Handgretinger, R., 25.11.2005, In: KLIN PADIATR. 217, 6, p. 334-8 5 p.

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

  49. A comparison between two semi-quantitative bleeding scales for the diagnosis and assessment of bleeding severity in type 1 von Willebrand disease.

    Tosetto, A., Rodeghiero, F., Castaman, G., Goodeve, A., Federici, A. B., Batlle, J., Meyer, D., Goudemand, J., Eikenboom, J., Schneppenheim, R., Budde, U., Ingerslev, J., Lethagen, S., Hill, F. G. H. & Peake, I., 2011, In: HAEMOPHILIA. 17, 1, p. 165-166 1.

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

  50. A complex karyotype in an atypical teratoid/rhabdoid tumor: case report and review of the literature.

    Coccé, M. C., Lubieniecki, F., Kordes, U., Alderete, D. & Gallego, M. S., 2011, In: J NEURO-ONCOL. 104, 1, p. 375-380 1.

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

  51. A conformational transition of the D'D3 domain primes von Willebrand factor for multimerization

    Gruber, S., Löf, A., Hausch, A., Kutzki, F., Jöhr, R., Obser, T., König, G., Schneppenheim, R., Aponte-Santamaría, C., Gräter, F., Brehm, M. A., Benoit, M. & Lipfert, J., 13.09.2022, In: BLOOD ADV. 6, 17, p. 5198-5209 12 p.

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

  52. Acquired hemophilia A and von Willebrand syndrome in a patient with late-onset systemic lupus erythematosus

    Dicke, C., Holstein, K., Schneppenheim, S., Dittmer, R., Schneppenheim, R., Bokemeyer, C., Iking-Konert, C., Budde, U. & Langer, F., 20.08.2014, In: EXP HEMATOL ONCOL. 3, p. 21

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

  53. Acquired von Willebrand syndrome as side effect of valproic acid therapy in children is rare.

    Eberl, W., Budde, U., Bentele, K. H. P., Christen, H-J., Knapp, R., Mey, A. & Schneppenheim, R., 2009, In: HAMOSTASEOLOGIE. 29, 2, p. 137-142 2.

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

  54. Acquired vorinostat resistance shows partial cross-resistance to 'second-generation' HDAC inhibitors and correlates with loss of histone acetylation and apoptosis but not with altered HDAC and HAT activities.

    Dedes, K. J., Dedes, I., Imesch, P., von Bueren, A., André, O., Fink, D. & Fedier, A., 2009, In: ANTI-CANCER DRUG. 20, 5, p. 321-333 5.

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

  55. Acquisition of granule neuron precursor identity is a critical determinant of progenitor cell competence to form Shh-induced medulloblastoma

    Schüller, U., Heine, V. M., Mao, J., Kho, A. T., Dillon, A. K., Han, Y-G., Huillard, E., Sun, T., Ligon, A. H., Qian, Y., Ma, Q., Alvarez-Buylla, A., McMahon, A. P., Rowitch, D. H. & Ligon, K. L., 12.08.2008, In: CANCER CELL. 14, 2, p. 123-34 12 p.

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

  56. Activated human hepatic stellate cells induce myeloid derived suppressor cells from peripheral blood monocytes in a CD44-dependent fashion

    Höchst, B., Schildberg, F. A., Sauerborn, P., Gäbel, Y. A., Gevensleben, H., Goltz, D., Heukamp, L. C., Türler, A., Ballmaier, M., Gieseke, F., Müller, I., Kalff, J., Kurts, C., Knolle, P. A. & Diehl, L., 01.09.2013, In: J HEPATOL. 59, 3, p. 528-35 8 p.

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

  57. Activated phosphoinositide 3-kinase δ syndrome: Update from the ESID Registry and comparison with other autoimmune-lymphoproliferative inborn errors of immunity

    Maccari, M. E., Wolkewitz, M., Schwab, C., Lorenzini, T., Leiding, J. W., Aladjdi, N., Abolhassani, H., Abou-Chahla, W., Aiuti, A., Azarnoush, S., Baris, S., Barlogis, V., Barzaghi, F., Baumann, U., Bloomfield, M., Bohynikova, N., Bodet, D., Boutboul, D., Bucciol, G., Buckland, M. S., Burns, S. O., Cancrini, C., Cathébras, P., Cavazzana, M., Cheminant, M., Chinello, M., Ciznar, P., Coulter, T. I., D'Aveni, M., Ekwall, O., Eric, Z., Eren, E., Fasth, A., Frange, P., Fournier, B., Garcia-Prat, M., Gardembas, M., Geier, C., Ghosh, S., Goda, V., Hammarström, L., Hauck, F., Heeg, M., Heropolitanska-Pliszka, E., Hilfanova, A., Jolles, S., Karakoc-Aydiner, E., Kindle, G. R., Kiykim, A., Klemann, C., Koletsi, P., Koltan, S., Kondratenko, I., Körholz, J., Krüger, R., Jeziorski, E., Levy, R., Le Guenno, G., Lefevre, G., Lougaris, V., Marzollo, A., Mahlaoui, N., Malphettes, M., Meinhardt, A., Merlin, E., Meyts, I., Milota, T., Moreira, F., Moshous, D., Mukhina, A., Neth, O., Neubert, J., Neven, B., Nieters, A., Nove-Josserand, R., Oksenhendler, E., Ozen, A., Olbrich, P., Perlat, A., Pac, M., Schmid, J. P., Pacillo, L., Parra-Martinez, A., Paschenko, O., Pellier, I., Sefer, A. P., Plebani, A., Plantaz, D., Prader, S., Raffray, L., Ritterbusch, H., Riviere, J. G., Rivalta, B., Rusch, S., Sakovich, I., Savic, S., Scheible, R., Schleinitz, N., Schuetz, C., Schulz, A., Sediva, A., Semeraro, M., Sharapova, S. O., Shcherbina, A., Slatter, M. A., Sogkas, G., Soler-Palacin, P., Speckmann, C., Stephan, J-L., Suarez, F., Tommasini, A., Trück, J., Uhlmann, A., van Aerde, K. J., van Montfrans, J., von Bernuth, H., Warnatz, K., Williams, T., Worth, A. J. J., Ip, W., Picard, C., Catherinot, E., Nademi, Z., Grimbacher, B., Forbes Satter, L. R., Kracker, S., Chandra, A., Condliffe, A. M., Ehl, S. & European Society for Immunodeficiencies Registry Working Party, 10.2023, In: J ALLERGY CLIN IMMUN. 152, 4, p. 984-996.e10

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

  58. Acute impact of an endurance race on cardiac function and biomarkers of myocardial injury in triathletes with and without myocardial fibrosis

    Tahir, E., Scherz, B., Starekova, J., Muellerleile, K., Fischer, R., Schoennagel, B., Warncke, M., Stehning, C., Cavus, E., Bohnen, S., Radunski, U. K., Blankenberg, S., Simon, P., Pressler, A., Adam, G., Patten, M. & Lund, G. K., 01.2020, In: EUR J PREV CARDIOL. 27, 1, p. 94-104 11 p.

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

  59. [Acute juvenile lymphoblastic leukemia]

    Haas, R. J., Janka-Schaub, G., Helmig, M. & Netzel, B., 1980, In: MMW Munch Med Wochenschr. 122, 9, p. 301-304 9.

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

  60. Acute lymphoblastic leukemia in children with Down Syndrome: a retrospective analysis from the Ponte di Legno study group

    Buitenkamp, T. D., Izraeli, S., Zimmermann, M., Forestier, E., Heerema, N. A., van den Heuvel-Eibrink, M. M., Pieters, R., Korbijn, C. M., Silverman, L. B., Schmiegelow, K., Liang, D-C., Horibe, K., Arico, M., Biondi, A., Basso, G., Rabin, K. R., Schrappe, M., Cario, G., Mann, G., Morak, M., Panzer-Grümayer, R., Mondelaers, V., Lammens, T., Cavé, H., Stark, B., Ganmore, I., Moorman, A. V., Vora, A., Hunger, S. P., Pui, C-H., Mullighan, C. G., Manabe, A., Escherich, G., Kowalczyk, J. R., Whitlock, J. A. & Zwaan, C. M., 02.01.2014, In: BLOOD. 123, 1, p. 70-77 8 p.

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  61. Adjuvant chemotherapy in osteosarcoma - effects of cisplatinum, BCD, and fibroblast interferon in sequential combination with HD-MTX and adriamycin. Preliminary results of the COSS 80 study.

    Winkler, K., Beron, G., Kotz, R., Salzer-Kuntschik, M., Beck, J., Beck, W., Brandeis, W., Ebell, W., Erttmann, R., Göbel, U., Havers, W., Henze, G., Hinderfield, L., Höcker, P., Jobke, A., Jürgens, H., Kabisch, H., Landbeck, G., Preusser, P., Prindull, G., Ramach, W., Ritter, J., Sekera, J., Treuner, J. & Wüst, G., 1983, In: J CANCER RES CLIN. 106, p. 1-7

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

  62. Adjuvant dendritic cell-based tumour vaccination for children with malignant brain tumours.

    Ardon, H., Steven, D. V., Frank, V. C., Claes, L., Kramm, C. M., Rutkowski, S., Wolff, J. E. A., Gool, V. & Stefaan, W., 2010, In: PEDIATR BLOOD CANCER. 54, 4, p. 519-525 4.

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  63. Administration of recombinant erythropoietin alone does not improve the phenotype in iron refractory iron deficiency anemia patients.

    Lehmberg, K., Grosse, R., Muckenthaler, M. U., Altamura, S., Nielsen, P., Schmid, H., Graubner, U., Oyen, F., Zeller, W., Schneppenheim, R. & Janka-Schaub, G., 2013, In: ANN HEMATOL. 92, 3, p. 387-394 3.

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  64. Adult and pediatric medulloblastomas are genetically distinct and require different algorithms for molecular risk stratification.

    Korshunov, A., Remke, M., Werft, W., Benner, A., Ryzhova, M., Witt, H., Sturm, D., Wittmann, A., Schöttler, A., Felsberg, J., Reifenberger, G., Rutkowski, S., Scheurlen, W., Kulozik, A. E., von Deimling, A., Lichter, P. & Pfister, S. M., 2010, In: J CLIN ONCOL. 28, 18, p. 3054-3060 18.

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

  65. Adult intracranial ependymoma-relevance of DNA methylation profiling for diagnosis, prognosis, and treatment

    Träger, M., Schweizer, L., Pérez, E., Schmid, S., Hain, E. G., Dittmayer, C., Onken, J., Fukuoka, K., Ichimura, K., Schüller, U., Dührsen, L., Müther, M., Paulus, W., Thomas, C., Gutt-Will, M., Schucht, P., Maragkou, T., Schittenhelm, J., Eckert, F., Niyazi, M., Fleischmann, D. F., Dorostkar, M. M., Feyer, P., May, S-A., Moskopp, D., Badakhshi, H., Radke, C., Walter, J., Ehret, F., Capper, D. & Kaul, D., 06.07.2023, In: NEURO-ONCOLOGY. 25, 7, p. 1286-1298 13 p.

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

  66. Adults with CNS primitive neuroectodermal tumors/pineoblastomas: results of multimodal treatment according to the pediatric HIT 2000 protocol

    Friedrich, C., Müller, K., von Hoff, K., Kwiecien, R., Pietsch, T., Warmuth-Metz, M., Gerber, N. U., Hau, P., Kuehl, J., Kortmann, R. D., von Bueren, A. O. & Rutkowski, S., 01.02.2014, In: J NEURO-ONCOL. 116, 3, p. 567-575 9 p.

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  67. Advancing multimer analysis of von Willebrand factor by single-molecule AFM imaging

    Löf, A., König, G., Schneppenheim, S., Schneppenheim, R., Benoit, M., Budde, U., Müller, J. P. & Brehm, M. A., 2019, In: PLOS ONE. 14, 1, p. e0210963

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  68. A fludarabine-based dose-reduced conditioning regimen followed by allogeneic stem cell transplantation from related or unrelated donors in patients with myelodysplastic syndrome.

    Kröger, N., Schetelig, J., Zabelina, T., Krüger, W., Renges, H., Stute, N., Schrum, J., Kabisch, H., Siegert, W. & Zander, A. R., 2001, In: BONE MARROW TRANSPL. 28, 7, p. 643-647 7.

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  69. A FOXO-Pak1 transcriptional pathway controls neuronal polarity

    de la Torre-Ubieta, L., Gaudillière, B., Yang, Y., Ikeuchi, Y., Yamada, T., DiBacco, S., Stegmüller, J., Schüller, U., Salih, D. A., Rowitch, D. H., Brunet, A. & Bonni, A., 15.04.2010, In: GENE DEV. 24, 8, p. 799-813 15 p.

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  70. Age and DNA-methylation subgroup as potential independent risk factors for treatment stratification in children with Atypical Teratoid/Rhabdoid Tumors (ATRT)

    Frühwald, M. C., Hasselblatt, M., Nemes, K., Bens, S., Steinbügl, M., Johann, P. D., Kerl, K., Hauser, P., Quiroga, E., Solano-Paez, P., Biassoni, V., Gil-da-Costa, M. J., Perek-Polnik, M., van de Wetering, M., Sumerauer, D., Pears, J., Stabell, N., Holm, S., Hengartner, H., Gerber, N. U., Grotzer, M., Boos, J., Ebinger, M., Tippelt, S., Paulus, W., Furtwängler, R., Hernáiz-Driever, P., Reinhard, H., Rutkowski, S., Schlegel, P-G., Schmid, I., Kortmann, R-D., Timmermann, B., Warmuth-Metz, M., Kordes, U., Gerss, J., Nysom, K., Schneppenheim, R., Siebert, R., Kool, M. & Graf, N., 07.07.2020, In: NEURO-ONCOLOGY. 22, 7, p. 1006–1017 12 p.

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  71. A heterozygous frameshift mutation in the Fanconi anemia C gene in familial T-ALL and secondary malignancy

    Rischewski, J. R., Clausen, H., Leber, V., Niemeyer, C., Ritter, J., Schindler, D. & Schneppenheim, R., 20.09.2000, In: KLIN PADIATR. 212, 4, p. 174-6 3 p.

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  72. Aktualisierte AWMF Leitlinie über die Diagnostik und Therapie der akuten lymphoblastische Leukämie im Kindesalter

    Escherich, G. & Schrappe, M., 11.2022, In: KLIN PADIATR. 234, 6, p. 363-367 5 p.

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  73. A large-scale method for T cell depletion: towards graft engineering of mobilized peripheral blood stem cells

    Gordon, P. R., Leimig, T., Mueller, I., Babarin-Dorner, A., Holladay, M. A., Houston, J., Kerst, G., Geiger, T. & Handgretinger, R., 07.2002, In: BONE MARROW TRANSPL. 30, 2, p. 69-74 6 p.

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  74. ALDH1A1 is a marker of astrocytic differentiation during brain development and correlates with better survival in glioblastoma patients

    Adam, S. A., Schnell, O., Pöschl, J., Eigenbrod, S., Kretzschmar, H. A., Tonn, J-C. & Schüller, U., 11.2012, In: BRAIN PATHOL. 22, 6, p. 788-97 10 p.

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  75. [All 77-01 therapy study for treatment of acute lymphocytic leukemia in childhood (author's transl)]

    Haas, R. J., Janka-Schaub, G., Netzel, B. & Helmig, M., 1981, In: KLIN PADIATR. 193, 3, p. 137-144 3.

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  76. Allergic-like reactions to asparaginase: Atypical allergies without asparaginase inactivation

    Kloos, R. Q. H., Pieters, R., Escherich, G. & van der Sluis, I. M., 04.07.2016, In: PEDIATR BLOOD CANCER. 63, 11, p. 1928-34

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  77. Allogeneic blood SCT for children with Hurler's syndrome: results from the German multicenter approach MPS-HCT 2005.

    Sauer, M., Meissner, B., Fuchs, D., Gruhn, B., Kabisch, H., Erttmann, R., Suttorp, M., Beilken, A., Luecke, T., Welte, K., Grigull, L. & Sykora, K. W., 2009, In: BONE MARROW TRANSPL. 43, 5, p. 375-381 5.

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  78. Allogeneic haematopoietic stem cell transplantation eliminates alloreactive inhibitory antibodies after liver transplantation for bile salt export pump deficiency

    Brinkert, F., Pukite, I., Krebs-Schmitt, D., Briem-Richter, A., Stindt, J., Häussinger, D., Keitel, V., Müller, I. & Grabhorn, E., 10.2018, In: J HEPATOL. 69, 4, p. 961-965 5 p.

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  79. Allogeneic hematopoietic cell transplantation for XIAP deficiency: an international survey reveals poor outcomes.

    Marsh, R. A., Rao, K., Satwani, P., Lehmberg, K., Müller, I., Li, D., Kim, M-O., Fischer, A., Latour, S., Sedlacek, P., Barlogis, V., Hamamoto, K., Kanegane, H., Milanovich, S., Margolis, D. A., Dimmock, D., Casper, J., Douglas, D. N., Amrolia, P. J., Veys, P., Kumar, A. R., Jordan, M. B., Bleesing, J. J. & Filipovich, A. H., 2013, In: BLOOD. 121, 6, p. 877-883 7 p., 6.

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  80. Allogeneic hematopoietic stem cell transplantation for adult HLH: a retrospective study by the chronic malignancies and inborn errors working parties of EBMT

    Machowicz, R., Suarez, F., Wiktor-Jedrzejczak, W., Eikema, D-J., de Wreede, L. C., Blok, H-J., Isaksson, C., Einsele, H., Poiré, X., van Dorp, S., Nikolousis, E., Johansson, J-E., Kobbe, G., Zecca, M., Arnold, R., Gerbitz, A., Finke, J., Díez-Martín, J. L., Bonifazi, F., McQuaker, G., Lenhoff, S., Rohrlich, P-S., Theobald, M., Ljungman, P., Collin, M., Albert, M. H., Ehninger, G., Carlson, K., Halaburda, K., Lehmberg, K., Schönland, S., Yakoub-Agha, I., Gennery, A. R., Lankester, A. C. & Kröger, N., 05.2022, In: BONE MARROW TRANSPL. 57, 5, p. 817-823 7 p.

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  81. Allogeneic hematopoietic stem cell transplantation from unrelated donors is associated with higher infection rates in children with acute lymphoblastic leukemia-A prospective international multicenter trial on behalf of the BFM-SG and the EBMT-PDWP

    Pichler, H., Lawitschka, A., Glogova, E., Willasch, A. M., von Luettichau, I., Lehrnbecher, T., Matthes-Martin, S., Lang, P., Bader, P., Sykora, K. W., Schrum, J., Kremens, B., Ehlert, K., Albert, M. H., Kuhlen, M., Meisel, R., Guengoer, T., Strahm, B., Gruhn, B., Schulz, A., Woessmann, W., Poetschger, U. & Peters, C., 08.2019, In: AM J HEMATOL. 94, 8, p. 880-890 11 p.

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  82. Allogeneic hematopoietic stem cell transplantation in two brothers with DNA ligase IV deficiency -a case report and review of the literature

    Schober, S., Schilbach, K., Doering, M., Cabanillas Stanchi, K. M., Holzer, U., Kasteleiner, P., Schittenhelm, J., Schaefer, J. F., Müller, I., Lang, P. & Handgretinger, R., 11.10.2019, In: BMC PEDIATR. 19, 1, p. 346

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  83. Almost normal cognitive function in patients during therapy for childhood acute lymphoblastic leukemia without cranial irradiation according to ALL-BFM 95 and COALL 06-97 protocols: results of an Austrian-German multicenter longitudinal study and implications for follow-up.

    Krappmann, P., Paulides, M., Stöhr, W., Ittner, E., Plattig, B., Nickel, P., Lackner, H., Schrappe, M., Janka-Schaub, G., Beck, J. D. & Langer, T., 2007, In: PEDIATR HEMAT ONCOL. 24, 2, p. 101-109 2.

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  84. A long duration of the prediagnostic symptomatic interval is not associated with an unfavourable prognosis in childhood medulloblastoma.

    Gerber, N. U., von Hoff, K., von Bueren, A., Treulieb, W., Treulieb, W., Deinlein, F., Benesch, M., Zwiener, I., Soerensen, N., Warmuth-Metz, M., Pietsch, T., Mittler, U., Kuehl, J., Kortmann, R-D., Rutkowski, S. & Rutkowski, S., 2012, In: EUR J CANCER. 48, 13, p. 2028-2036 13.

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  85. alpha-Melanocyte-stimulating hormone signaling regulates expression of microphthalmia, a gene deficient in Waardenburg syndrome.

    Price, E. R., Horstmann, M., Wells, A. G., Weilbaecher, K. N., Takemoto, C. M., Landis, M. W. & Fisher, D. E., 1998, In: J BIOL CHEM. 273, 49, p. 33042-33047 49.

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  86. Alteration in GPIIb/IIIa Binding of VWD-Associated von Willebrand Factor Variants with C-Terminal Missense Mutations

    König, G., Obser, T., Marggraf, O., Schneppenheim, S., Budde, U., Schneppenheim, R. & Brehm, M. A., 07.2019, In: THROMB HAEMOSTASIS. 119, 7, p. 1102-1111 10 p.

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  87. 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.

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  88. A molecular approach to the classification of von Willebrand disease

    Schneppenheim, R., Budde, U. & Ruggeri, Z. M., 01.06.2001, In: BEST PRACT RES CL HA. 14, 2, p. 281-98 18 p.

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  89. A mouse model for embryonal tumors with multilayered rosettes uncovers the therapeutic potential of Sonic-hedgehog inhibitors

    Neumann, J. E., Wefers, A. K., Lambo, S., Bianchi, E., Bockstaller, M., Dorostkar, M. M., Meister, V., Schindler, P., Korshunov, A., von Hoff, K., Nowak, J., Warmuth-Metz, M., Schneider, M. R., Renner-Müller, I., Merk, D. J., Shakarami, M., Sharma, T., Chavez, L., Glass, R., Chan, J. A., Taketo, M. M., Neumann, P., Kool, M. & Schüller, U., 10.2017, In: NAT MED. 23, 10, p. 1191-1202

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

  90. Amplification of the PLAG-family genes-PLAGL1 and PLAGL2-is a key feature of the novel tumor type CNS embryonal tumor with PLAGL amplification

    Keck, M-K., Sill, M., Wittmann, A., Joshi, P., Stichel, D., Beck, P., Okonechnikow, K., Sievers, P., Wefers, A. K., Roncaroli, F., Avula, S., McCabe, M. G., Hayden, J. T., Wesseling, P., Øra, I., Nistér, M., Kranendonk, M. E. G., Tops, B. B. J., Zapotocky, M., Zamecnik, J., Vasiljevic, A., Fenouil, T., Meyronet, D., von Hoff, K., Schüller, U., Loiseau, H., Figarella-Branger, D., Kramm, C. M., Sturm, D., Scheie, D., Rauramaa, T., Pesola, J., Gojo, J., Haberler, C., Brandner, S., Jacques, T., Sexton Oates, A., Saffery, R., Koscielniak, E., Baker, S. J., Yip, S., Snuderl, M., Ud Din, N., Samuel, D., Schramm, K., Blattner-Johnson, M., Selt, F., Ecker, J., Milde, T., von Deimling, A., Korshunov, A., Perry, A., Pfister, S. M., Sahm, F., Solomon, D. A. & Jones, D. T. W., 01.2023, In: ACTA NEUROPATHOL. 145, 1, p. 49-69 21 p.

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

  91. Amsacrine combined with etoposide and high-dose methylprednisolone as salvage therapy in acute lymphoblastic leukemia in children.

    Horstmann, M., Hassenpflug, W-A., Udo, Z. S., Escherich, G., Janka-Schaub, G. & Kabisch, H., 2005, In: HAEMATOLOGICA. 90, 12, p. 1701-1703 12.

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  92. Amsacrine combined with etoposide and methylprednisolone is a feasible and safe component in first-line intensified treatment of pediatric patients with high-risk acute lymphoblastic leukemia in CoALL08-09 trial

    Mezger, K., Ebert, S., Muhle, H. E., Stadt, U. Z., Borkhardt, A., Dilloo, D., Faber, J., Feuchtinger, T., Imschweiler, T., Jorch, N., Pekrun, A., Schmid, I., Schramm, F., Zimmermann, M., Horstmann, M. A. & Escherich, G., 12.2022, In: PEDIATR BLOOD CANCER. 69, 12, e29997.

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

  93. A multicenter study of patients with multisystem Langerhans cell histiocytosis who develop secondary hemophagocytic lymphohistiocytosis

    Chellapandian, D., Hines, M. R., Zhang, R., Jeng, M., van den Bos, C., Santa-María López, V., Lehmberg, K., Sieni, E., Wang, Y., Nakano, T., Williams, J. A., Fustino, N. J., Astigarraga, I., Dunkel, I. J., Abla, O., van Halteren, A. G. S., Pei, D., Cheng, C., Weitzman, S., Sung, L. & Nichols, K. E., 15.03.2019, In: CANCER-AM CANCER SOC. 125, 6, p. 963-971 9 p.

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

  94. A multi-institutional retrospective pooled outcome analysis of molecularly annotated pediatric supratentorial ZFTA-fused ependymoma

    Ng, C. H., Obrecht, D., Wells, O., Zapotocky, M., Sumerauer, D., Coltin, H., Khuong-Quang, D-A., Eisenstat, D. D., Kinross, K. M., White, C. L., Algar, E. M., Luck, A., Witt, H., Schüller, U., Mynarek, M., Pietsch, T., Gerber, N. U., Benesch, M., Warmuth-Metz, M., Kortmann, R., Bison, B., Taylor, M. D., Rutkowski, S., Pfister, S. M., Jones, D. T., Gottardo, N. G., von Hoff, K., Pajtler, K. W., Ramaswamy, V. & Hansford, J. R., 2023, In: NEURO-ONCOL ADV. 5, 1, p. vdad057

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

  95. A Multimodal Lifestyle Psychosocial Survivorship Program in Young Cancer Survivors: The CARE for CAYA Program-A Randomized Clinical Trial Embedded in a Longitudinal Cohort Study

    von Grundherr, J., Elmers, S., Koch, B., Hail, L-A., Mann, J., Escherich, G., Bergelt, C., Samland, L., Jensen, W., Vettorazzi, E., Stark, M., Valentini, L., Baumann, F. T., Singer, S., Reer, R., Beller, R., Calaminus, G., Faber, J., Classen, C. F., Gebauer, J., Hilgendorf, I., Koehler, M., Puzik, A., Salzmann, N., Sander, A., Schiffmann, L., Sokalska-Duhme, M., Schuster, S., Kock-Schoppenhauer, A-K., Bokemeyer, C., Sinn, M., Stein, A., Dwinger, S. & Salchow, J., 04.03.2024, In: JAMA NETW OPEN. 7, 3, p. e242375

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

  96. A multi-omics approach reveals mechanisms of nanomaterial toxicity and structure-activity relationships in alveolar macrophages

    Bannuscher, A., Karkossa, I., Buhs, S., Nollau, P., Kettler, K., Balas, M., Dinischiotu, A., Hellack, B., Wiemann, M., Luch, A., von Bergen, M., Haase, A. & Schubert, K., 03.2020, In: NANOTOXICOLOGY. 14, 2, p. 181-195 15 p.

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  97. An 8-Year-Old Girl with Posterior Fossa Mass

    Ruf, V. C., Schöler, A., Capper, D., Arzberger, T., Herms, J. & Schüller, U., 05.2020, In: BRAIN PATHOL. 30, 3, p. 713-714 2 p.

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  98. An additional unique candidate mutation (G2470A; M740I) in the original families with von Willebrand disease type 2 M Vicenza and the G3864A (R1205H) mutation

    Castaman, G., Missiaglia, E., Federici, A. B., Schneppenheim, R. & Rodeghiero, F., 01.08.2000, In: THROMB HAEMOSTASIS. 84, 2, p. 350-1 2 p.

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  99. An aggressive systemic juvenile xanthogranuloma clonally related to a preceding T-cell acute lymphoblastic leukemia.

    Perez-Becker, R., Szczepanowski, M., Leuschner, I., Janka-Schaub, G., Gokel, M., Imschweiler, T., Völpel, S., Niehues, T. & Klapper, W., 2011, In: PEDIATR BLOOD CANCER. 56, 5, p. 859-862 5.

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  100. An Alu-mediated novel large deletion is the most frequent cause of type 3 von Willebrand disease in Hungary.

    Mohl, A., Marschalek, R., Masszi, T., Nagy, E., Obser, T., Oyen, F., Sallai, K., Bodó, I. & Schneppenheim, R., 2008, In: J THROMB HAEMOST. 6, 10, p. 1729-1735 10.

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  101. Analysis of a cohort of 101 CDAII patients: description of 24 new molecular variants and genotype-phenotype correlations

    Bianchi, P., Schwarz, K., Högel, J., Fermo, E., Vercellati, C., Grosse, R., van Wijk, R., van Zwieten, R., Barcellini, W., Zanella, A. & Heimpel, H., 11.2016, In: BRIT J HAEMATOL. 175, 4, p. 696-704 9 p.

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  102. Analysis of minimal residual disease by Ig/TCR gene rearrangements: guidelines for interpretation of real-time quantitative PCR data.

    van der Velden, V. H. J., Cazzaniga, G., Schrauder, A., Hancock, J., Bader, P., Panzer-Grumayer, E. R., Flohr, T., Sutton, R., Cave, H., Madsen, H. O., Cayuela, J. M., Trka, J., Eckert, C., Foroni, L., Zur Stadt, U., Beldjord, K., Raff, T., van der Schoot, C. E. & van Dongen, J. J. M., 2007, In: LEUKEMIA. 21, 4, p. 604-611 4.

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

  103. Analysis of posaconazole as oral antifungal prophylaxis in pediatric patients under 12 years of age following allogeneic stem cell transplantation.

    Döring, M., Müller, C., Johann, P-D., Erbacher, A., Kimmig, A., Schwarze, C-P., Lang, P., Handgretinger, R. & Müller, I., 2012, In: BMC INFECT DIS. 12, p. 263

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

  104. Analysis of sternotomy as treatment option for the resection of bilateral pulmonary metastases in pediatric solid tumors

    Fuchs, J., Seitz, G., Ellerkamp, V., Dietz, K., Bosk, A., Müller, I., Warmann, S. W. & Schäfer, J. F., 12.2008, In: J SURG ONCOL. 17, 4, p. 323-30 8 p.

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  105. Analysis of the CC chemokine receptor 5Delta32 polymorphism in pediatric liver transplant recipients.

    Fischer-Maas, L., Schneppenheim, R., Oyen, F., Grabhorn, E., Briem-Richter, A., Fischer, L. & Ganschow, R., 2008, In: PEDIATR TRANSPLANT. 12, 7, p. 769-772 7.

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

  106. Analysis of treatment efficiency of carboplatin and etoposide in combination with radical surgery in advanced and recurrent childhood hepatoblastoma: a report of the German Cooperative Pediatric Liver Tumor Study HB 89 and HB 94.

    Fuchs, J., Bode, U., von Schweinitz, D., Weinel, P., Erttmann, R., Harms, D. & Mildenberger, H., 1999, In: KLIN PADIATR. 211, 4, p. 305-309 4.

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

  107. Analyzing expression and phosphorylation of the EGF receptor in HNSCC

    Kriegs, M., Clauditz, T. S., Hoffer, K., Bartels, J., Buhs, S., Gerull, H., Zech, H. B., Bußmann, L., Struve, N., Rieckmann, T., Petersen, C., Betz, C. S., Rothkamm, K., Nollau, P. & Münscher, A., 19.09.2019, In: SCI REP-UK. 9, 1, p. 13564

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

  108. Analyzing tyrosine kinase activity in head and neck cancer by functional kinomics: Identification of hyperactivated Src-family kinases as prognostic markers and potential targets

    Bußmann, L., Hoffer, K., von Bargen, C. M., Droste, C., Lange, T., Kemmling, J., Schröder-Schwarz, J., Vu, A. T., Akingunsade, L., Nollau, P., Rangarajan, S., de Wijn, R., Oetting, A., Müller, C., Böckelmann, L. C., Zech, H. B., Berger, J. C., Möckelmann, N., Busch, C-J., Böttcher, A., Gatzemeier, F., Klinghammer, K., Simnica, D., Binder, M., Struve, N., Rieckmann, T., Schumacher, U., Clauditz, T. S., Betz, C. S., Petersen, C., Rothkamm, K., Münscher, A. & Kriegs, M., 01.09.2021, In: INT J CANCER. 149, 5, p. 1166 - 1180 15 p.

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

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