Research ExplorerResearch UnitsCenter for Obstetrics and Pediatrics Publications

Center for Obstetrics and Pediatrics

2501 - 2550 out of 4,516Page size: 50

Publications

  1. 2013

  2. Is rituximab effective in childhood nephrotic syndrome? Yes and no

    Kemper, M. J., Lehnhardt, A., Zawischa, A. & Oh, J., 03.07.2013, In: PEDIATR NEPHROL.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  3. Ultralarge von Willebrand factor fibers mediate luminal Staphylococcus aureus adhesion to an intact endothelial cell layer under shear stress

    Pappelbaum, K. I., Gorzelanny, C., Grässle, S., Suckau, J., Laschke, M. W., Bischoff, M., Bauer, C., Schorpp-Kistner, M., Weidenmaier, C., Schneppenheim, R., Obser, T., Sinha, B. & Schneider, S. W., 02.07.2013, In: CIRCULATION. 128, 1, p. 50-9 10 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  4. Development of a mnemonic screening tool for identifying subjects with Hunter syndrome

    Cohn, G. M., Morin, I., Whiteman, D. A. H. & Hunter Outcome Survey Investigators, 01.07.2013, In: EUR J PEDIATR. 172, 7, p. 965-70 6 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  5. Diagnosis of Pompe disease: muscle biopsy vs blood-based assays

    Vissing, J., Lukacs, Z. & Straub, V., 01.07.2013, In: JAMA NEUROL. 70, 7, p. 923-7 5 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  6. Eisenquantifizierung mittels MRT bei Eisenüberladung

    Schönnagel, B. P., Fischer, R., Nielsen, P., Grosse, R., Adam, G. & Yamamura, J., 01.07.2013, In: ROFO-FORTSCHR RONTG. 185, 7, p. 621-7 7 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  7. Genetic screening in adolescents with steroid-resistant nephrotic syndrome

    Lipska, B. S., Iatropoulos, P., Maranta, R., Caridi, G., Ozaltin, F., Anarat, A., Balat, A., Gellermann, J., Trautmann, A., Erdogan, O., Saeed, B., Emre, S., Bogdanovic, R., Azocar, M., Balasz-Chmielewska, I., Benetti, E., Caliskan, S., Mir, S., Melk, A., Ertan, P., Baskin, E., Jardim, H., Davitaia, T., Wasilewska, A., Drozdz, D., Szczepanska, M., Jankauskiene, A., Higuita, L. M. S., Ardissino, G., Ozkaya, O., Kuzma-Mroczkowska, E., Soylemezoglu, O., Ranchin, B., Medynska, A., Tkaczyk, M., Peco-Antic, A., Akil, I., Jarmolinski, T., Firszt-Adamczyk, A., Dusek, J., Simonetti, G. D., Gok, F., Gheissari, A., Emma, F., Krmar, R. T., Fischbach, M., Printza, N., Simkova, E., Mele, C., Ghiggeri, G. M., Schaefer, F. & PodoNet Consortium, 01.07.2013, In: KIDNEY INT. 84, 1, p. 206-13 8 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  8. Identification of a homozygous Cys410Ser mutation in the von Willebrand factor D2 domain causing type 2A(IIC) von Willebrand disease phenotype in an Iranian patient

    Enayat, M. S., Ravanbod, S., Rassoulzadegan, M., Jazebi, M., Ala, F., Budde, U., Schneppenheim, S., Obser, T. & Schneppenheim, R., 01.07.2013, In: HAEMOPHILIA. 19, 4, p. e261-4

    Research output: SCORING: Contribution to journal › Other (editorial matter etc.) › Research

  9. Outcomes of treatment for relapsed acute lymphoblastic leukaemia in children with Down syndrome

    Meyr, F., Escherich, G., Mann, G., Klingebiel, T., Kulozik, A., Rossig, C., Schrappe, M., Henze, G., von Stackelberg, A. & Hitzler, J., 01.07.2013, In: BRIT J HAEMATOL. 162, 1, p. 98-106 9 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  10. Phenotype and genotype in 101 males with X-linked creatine transporter deficiency

    van de Kamp, J. M., Betsalel, O. T., Mercimek-Mahmutoglu, S., Abulhoul, L., Grünewald, S., Anselm, I., Azzouz, H., Bratkovic, D., de Brouwer, A., Hamel, B., Kleefstra, T., Yntema, H., Campistol, J., Vilaseca, M. A., Cheillan, D., D'Hooghe, M., Diogo, L., Garcia, P., Valongo, C., Fonseca, M., Frints, S., Wilcken, B., von der Haar, S., Meijers-Heijboer, H. E., Hofstede, F., Johnson, D., Kant, S. G., Lion-Francois, L., Pitelet, G., Longo, N., Maat-Kievit, J. A., Monteiro, J. P., Munnich, A., Muntau, A. C., Nassogne, M. C., Osaka, H., Ounap, K., Pinard, J. M., Quijano-Roy, S., Poggenburg, I., Poplawski, N., Abdul-Rahman, O., Ribes, A., Arias, A., Yaplito-Lee, J., Schulze, A., Schwartz, C. E., Schwenger, S., Soares, G., Sznajer, Y., Valayannopoulos, V., Van Esch, H., Waltz, S., Wamelink, M. M. C., Pouwels, P. J. W., Errami, A., van der Knaap, M. S., Jakobs, C., Mancini, G. M. & Salomons, G. S., 01.07.2013, In: J MED GENET. 50, 7, p. 463-72 10 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  11. Second malignant neoplasms after treatment of childhood acute lymphoblastic leukemia

    Schmiegelow, K., Levinsen, M. F., Attarbaschi, A., Baruchel, A., Devidas, M., Escherich, G., Gibson, B., Heydrich, C., Horibe, K., Ishida, Y., Liang, D-C., Locatelli, F., Michel, G., Pieters, R., Piette, C., Pui, C-H., Raimondi, S., Silverman, L., Stanulla, M., Stark, B., Winick, N. & Valsecchi, M. G., 01.07.2013, In: J CLIN ONCOL. 31, 19, p. 2469-76 8 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  12. Twin anemia-polycythemia sequence in a case of monoamniotic twins

    Diehl, W., Glosemeyer, P., Tavares De Sousa, M., Hollwitz, B., Ortmeyer, G. & Hecher, K., 01.07.2013, In: ULTRASOUND OBST GYN. 42, 1, p. 108-11 4 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  13. Recurrent multiple spinal paragangliomas as a manifestation of a metastatic composite paraganglioma-ganglioneuroblastoma

    Gempt, J., Baldawa, S. S., Weirich, G., Delbridge, C., Hempel, M., Lohse, P., Meyer, B. & Ringel, F., 07.2013, In: ACTA NEUROCHIR. 155, 7, p. 1241-2 2 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  14. Sox2 requirement in sonic hedgehog-associated medulloblastoma

    Ahlfeld, J., Favaro, R., Pagella, P., Kretzschmar, H. A., Nicolis, S. & Schüller, U., 15.06.2013, In: CANCER RES. 73, 12, p. 3796-807 12 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  15. Denosumab: a potential new and innovative treatment option for aneurysmal bone cysts

    Lange, T., Stehling, C., Fröhlich, B., Klingenhöfer, M., Kunkel, P., Schneppenheim, R., Escherich, G., Gosheger, G., Hardes, J., Jürgens, H. & Schulte, T. L., 01.06.2013, In: EUR SPINE J. 22, 6, p. 1417-22 6 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  16. Differentiating macrophage activation syndrome in systemic juvenile idiopathic arthritis from other forms of hemophagocytic lymphohistiocytosis

    Lehmberg, K., Pink, I., zu Eulenburg, C., Beutel, K., Maul-Pavicic, A. & Janka-Schaub, G., 01.06.2013, In: J PEDIATR-US. 162, 6, p. 1245-51 7 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  17. Long-term follow-up and outcome of phenylketonuria patients on sapropterin: a retrospective study

    Keil, S., Anjema, K., van Spronsen, F. J., Lambruschini, N., Burlina, A., Bélanger-Quintana, A., Couce, M. L., Feillet, F., Cerone, R., Lotz-Havla, A. S., Muntau, A. C., Bosch, A. M., Meli, C. A. P., Billette de Villemeur, T., Kern, I., Riva, E., Giovannini, M., Damaj, L., Leuzzi, V. & Blau, N., 01.06.2013, In: PEDIATRICS. 131, 6, p. e1881-8

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  18. MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis

    Lill, C. M., Schjeide, B-M. M., Graetz, C., Ban, M., Alcina, A., Ortiz, M. A., Pérez, J., Damotte, V., Booth, D., Lopez de Lapuente, A., Broer, L., Schilling, M., Akkad, D. A., Aktas, O., Alloza, I., Antigüedad, A., Arroyo, R., Blaschke, P., Buttmann, M., Chan, A., Compston, A., Cournu-Rebeix, I., Dörner, T., Epplen, J. T., Fernández, Ó., Gerdes, L-A., Guillot-Noël, L., Hartung, H-P., Hoffjan, S., Izquierdo, G., Kemppinen, A., Kroner, A., Kubisch, C., Kümpfel, T., Li, S-C., Lindenberger, U., Lohse, P., Lubetzki, C., Luessi, F., Malhotra, S., Mescheriakova, J., Montalban, X., Papeix, C., Paredes, L. F., Rieckmann, P., Steinhagen-Thiessen, E., Winkelmann, A., Zettl, U. K., Hintzen, R., Vandenbroeck, K., Stewart, G., Fontaine, B., Comabella, M., Urcelay, E., Matesanz, F., Sawcer, S., Bertram, L., Zipp, F. & International Multiple Sclerosis Genetics Consortium (IMSGC), 01.06.2013, In: BRAIN. 136, Pt 6, p. 1778-82 5 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  19. Pontocerebellar hypoplasia type 2 and TSEN2: review of the literature and two novel mutations

    Bierhals, T., Korenke, G. C., Uyanik, G. & Kutsche, K., 01.06.2013, In: EUR J MED GENET. 56, 6, p. 325-30 6 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  20. Robust molecular subgrouping and copy-number profiling of medulloblastoma from small amounts of archival tumour material using high-density DNA methylation arrays

    Hovestadt, V., Remke, M., Kool, M., Pietsch, T., Northcott, P. A., Fischer, R., Cavalli, F. M. G., Ramaswamy, V., Zapatka, M., Reifenberger, G., Rutkowski, S., Schick, M., Bewerunge-Hudler, M., Korshunov, A., Lichter, P., Taylor, M. D., Pfister, S. M. & Jones, D. T. W., 01.06.2013, In: ACTA NEUROPATHOL. 125, 6, p. 913-6 4 p.

    Research output: SCORING: Contribution to journal › Other (editorial matter etc.) › Research

  21. Therapeutic potential of the poly(ADP-ribose) polymerase inhibitor rucaparib for the treatment of sporadic human ovarian cancer

    Henningsen, M., zu Eulenburg, C., Kolarova, T., Qi, J. W., Manivong, K., Chalukya, M., Dering, J., Anderson, L., Ginther, C., Meuter, A., Winterhoff, B., Jones, S., Velculescu, V. E., Venkatesan, N., Rong, H-M., Dandekar, S., Udar, N., Jänicke, F., Los, G., Slamon, D. J. & Konecny, G. E., 01.06.2013, In: MOL CANCER THER. 12, 6, p. 1002-15 14 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  22. Ungewöhnlicher Haut- und Skelettbefund – Infantile Myofibromatose

    Warlitz, C., Kobbe, R., Helmke, K., Höger, P. & Singer, D., 01.06.2013, In: Z GEBURTSH NEONATOL. 217, 3, p. 112-3 2 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  23. Anal atresia, coloboma, microphthalmia, and nasal skin tag in a female patient with 3.5 Mb deletion of 3q26 encompassing SOX2

    Salem, N. J. M., Hempel, M., Heiliger, K-J., Hosie, S., Meitinger, T. & Oexle, K., 06.2013, In: AM J MED GENET A. 161A, 6, p. 1421-4 4 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  24. A novel phosphorylation site mutation in profilin 1 revealed in a large screen of US, Nordic, and German amyotrophic lateral sclerosis/frontotemporal dementia cohorts

    Ingre, C., Landers, J. E., Rizik, N., Volk, A. E., Akimoto, C., Birve, A., Hübers, A., Keagle, P. J., Piotrowska, K., Press, R., Andersen, P. M., Ludolph, A. C. & Weishaupt, J. H., 06.2013, In: NEUROBIOL AGING. 34, 6, p. 1708.e1-6

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  25. Hereditary thrombotic thrombocytopenic purpura and the hereditary TTP registry

    Mansouri Taleghani, M., von Krogh, A-S., Fujimura, Y., George, J. N., Hrachovinová, I., Knöbl, P. N., Quist-Paulsen, P., Schneppenheim, R., Lämmle, B. & Kremer Hovinga, J. A., 29.05.2013, In: HAMOSTASEOLOGIE. 33, 2, p. 138-43 6 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  26. Pregnancy in Upshaw-Schulman syndrome

    Kentouche, K., Voigt, A., Schleussner, E., Schneppenheim, R., Budde, U., Beck, J. F., Stefańska-Windyga, E. & Windyga, J., 29.05.2013, In: HAMOSTASEOLOGIE. 33, 2, p. 144-8 5 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  27. Allo-SCT using BU, CY and melphalan for children with AML in second CR

    Beier, R., Albert, M. H., Bader, P., Borkhardt, A., Creutzig, U., Eyrich, M., Ehlert, K., Gruhn, B., Greil, J., Handgretinger, R., Holter, W., Klingebiel, T., Kremens, B., Lang, P., Mauz-Körholz, C., Meisel, R., Müller, I., Peters, C., Reinhardt, D., Sedlacek, P., Schulz, A., Schuster, F. R., Schrauder, A., Strahm, B., Sykora, K. W., Wössmann, W., Zimmermann, M. & Sauer, M. G., 01.05.2013, In: BONE MARROW TRANSPL. 48, 5, p. 651-6 6 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Transfer › peer-review

  28. Ethnic-Specific WRN Mutations in South Asian Werner Syndrome Patients: Potential Founder Effect in Patients with Indian or Pakistani Ancestry

    Saha, B., Lessel, D., Nampoothiri, S., Rao, A. S., Hisama, F. M., Peter, D., Bennett, C., Nürnberg, G., Nürnberg, P., Martin, G. M., Kubisch, C. & Oshima, J., 01.05.2013, In: MOL GENET GENOM MED. 1, 1, p. 7-14 8 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  29. Peripartale Kardiomyopathie: Interdisziplinäre Herausforderung

    Löser, B., Tank, S., Hillebrand, G., Goldmann, B., Diehl, W., Biermann, D., Schirmer, J. & Reuter, D. A., 01.05.2013, In: ANAESTHESIST. 62, 5, p. 343-54 12 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  30. Reelin and the Cdc42/Rac1 guanine nucleotide exchange factor αPIX/Arhgef6 promote dendritic Golgi translocation in hippocampal neurons

    Meseke, M., Rosenberger, G. & Förster, E., 01.05.2013, In: EUR J NEUROSCI. 37, 9, p. 1404-12 9 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  31. The effect of idursulfase on growth in patients with Hunter Syndrome: data from the Hunter Outcome Survey (HOS)

    Jones, S. A., Parini, R., Harmatz, P., Giugliani, R., Fang, J., Mendelsohn, N. J. & HOS Natural History Working Group on behalf of HOS Investigators, 01.05.2013, In: MOL GENET METAB. 109, 1, p. 41-8 8 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  32. What's in a name? Intracranial peripheral primitive neuroectodermal tumors and CNS primitive neuroectodermal tumors are not the same

    Müller, K., Diez, B., Muggeri, A., Pietsch, T., Friedrich, C., Rutkowski, S., von Hoff, K., von Bueren, A. O., Zwiener, I. & Bruns, F., 01.05.2013, In: STRAHLENTHER ONKOL. 189, 5, p. 372-9 8 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  33. A novel optineurin truncating mutation and three glaucoma-associated missense variants in patients with familial amyotrophic lateral sclerosis in Germany

    Weishaupt, J. H., Waibel, S., Birve, A., Volk, A. E., Mayer, B., Meyer, T., Ludolph, A. C. & Andersen, P. M., 05.2013, In: NEUROBIOL AGING. 34, 5, p. 1516.e9-15

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  34. Deciphering the glycosylome of dystroglycanopathies using haploid screens for lassa virus entry

    Jae, L. T., Raaben, M., Riemersma, M., van Beusekom, E., Blomen, V. A., Velds, A., Kerkhoven, R. M., Carette, J. E., Topaloglu, H., Meinecke, P., Wessels, M. W., Lefeber, D. J., Whelan, S. P., van Bokhoven, H. & Brummelkamp, T. R., 26.04.2013, In: SCIENCE. 340, 6131, p. 479-83 5 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  35. Incidence and prognostic relevance of genetic variations in T-cell lymphoblastic lymphoma in childhood and adolescence

    Bonn, B. R., Rohde, M., Zimmermann, M., Krieger, D., Oschlies, I., Niggli, F., Wrobel, G., Attarbaschi, A., Escherich, G., Klapper, W., Reiter, A. & Burkhardt, B., 18.04.2013, In: BLOOD. 121, 16, p. 3153-60 8 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  36. Functional analysis of a duplication (p.E63_D69dup) in the switch II region of HRAS: new aspects of the molecular pathogenesis underlying Costello syndrome

    Lorenz, S., Lissewski, C., Simsek-Kiper, P. O., Alanay, Y., Boduroglu, K., Zenker, M. & Rosenberger, G., 15.04.2013, In: HUM MOL GENET. 22, 8, p. 1643-53 11 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  37. The risk of hemophagocytic lymphohistiocytosis in Hermansky-Pudlak syndrome type 2

    Jessen, B., Bode, S. F. N., Ammann, S., Chakravorty, S., Davies, G., Diestelhorst, J., Frei-Jones, M., Gahl, W. A., Gochuico, B. R., Griese, M., Griffiths, G., Janka-Schaub, G., Klein, C., Kögl, T., Kurnik, K., Lehmberg, K., Maul-Pavicic, A., Mumford, A. D., Pace, D., Parvaneh, N., Rezaei, N., de Saint Basile, G., Schmitt-Graeff, A., Schwarz, K., Karasu, G. T., Zieger, B., zur Stadt, U., Aichele, P. & Ehl, S., 11.04.2013, In: BLOOD. 121, 15, p. 2943-51 9 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  38. Gender differences in solitary functioning kidney: do they affect renal outcome? Response

    Kummer, S. & Oh, J., 10.04.2013, In: PEDIATR NEPHROL.

    Research output: SCORING: Contribution to journal › Other (editorial matter etc.) › Research

  39. Deficiency in SLC25A1, encoding the mitochondrial citrate carrier, causes combined D-2- and L-2-hydroxyglutaric aciduria

    Nota, B., Struys, E. A., Pop, A., Jansen, E. E., Fernandez Ojeda, M. R., Kanhai, W. A., Kranendijk, M., van Dooren, S. J. M., Bevova, M. R., Sistermans, E. A., Nieuwint, A. W. M., Barth, M., Ben-Omran, T., Hoffmann, G. F., de Lonlay, P., McDonald, M. T., Meberg, A., Muntau, A., Nuoffer, J-M., Parini, R., Read, M-H., Renneberg, A., Santer, R., Strahleck, T., van Schaftingen, E., van der Knaap, M. S., Jakobs, C. & Salomons, G. S., 04.04.2013, In: AM J HUM GENET. 92, 4, p. 627-31 5 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  40. Distinct role of von Willebrand factor triplet bands in glycoprotein Ib-dependent platelet adhesion and thrombus formation under flow

    Fuchs, B., de Witt, S., Solecka, B. A., Kröning, M., Obser, T., Cosemans, J. M. E. M., Schneppenheim, R., Heemskerk, J. W. M. & Kannicht, C., 01.04.2013, In: SEMIN THROMB HEMOST. 39, 3, p. 306-14 9 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  41. Editorial

    Diemert, A., 01.04.2013, In: Z GEBURTSH NEONATOL. 217, 2, p. 41

    Research output: SCORING: Contribution to journal › Other (editorial matter etc.) › Transfer

  42. Exon 2 duplication of the MID1 gene in a patient with a mild phenotype of Opitz G/BBB syndrome

    Hüning, I., Kutsche, K., Rajaei, S., Erlandsson, A., Lovmar, L., Rundberg, J. & Stefanova, M., 01.04.2013, In: EUR J MED GENET. 56, 4, p. 188-91 4 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  43. Fehlbildungen der Niere und ableitenden Harnwege – Autosomal-rezessive polyzystische Nierenerkrankung (ARPKD)

    Diemert, A., Klaassen, I., Kemper, M. J., Hecher, K. & Singer, D., 01.04.2013, In: Z GEBURTSH NEONATOL. 217, 2, p. 46-9 4 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  44. Phenotypic and molecular characterisation of type 3 von Willebrand disease in a cohort of Indian patients

    Ahmad, F., Budde, U., Jan, R., Oyen, F., Kannan, M., Saxena, R. & Schneppenheim, R., 01.04.2013, In: THROMB HAEMOSTASIS. 109, 4, p. 652-60 9 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  45. Rectum perforation after broomstick impalement in a 17-year-old: case report and review

    Boettcher, M., Kanellos-Becker, I., Wenke, K. & Krebs, T. F., 01.04.2013, In: PEDIATR EMERG CARE. 29, 4, p. 510-2 3 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  46. Seltene Fehlbildung der Anogenitalregion – Fetale Enterolithiasis als Vorbote einer Penisagenesie

    Hillebrand, G., Glosemeyer, P., Helmke, K. & Singer, D., 01.04.2013, In: Z GEBURTSH NEONATOL. 217, p. 72-73

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  47. Supra- and infratentorial pediatric ependymomas differ significantly in NeuN, p75 and GFAP expression

    Hagel, C., Treszl, A., Fehlert, J., Harder, J., von Haxthausen, F., Kern, M., von Bueren, A. O. & Kordes, U., 01.04.2013, In: J NEURO-ONCOL. 112, 2, p. 191-7 7 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  48. VWF propeptide and ratios between VWF, VWF propeptide, and FVIII in the characterization of type 1 von Willebrand disease

    Eikenboom, J., Federici, A. B., Dirven, R. J., Castaman, G., Rodeghiero, F., Budde, U., Schneppenheim, R., Batlle, J., Canciani, M. T., Goudemand, J., Peake, I., Goodeve, A. & MCMDM-1VWD Study Group, 21.03.2013, In: BLOOD. 121, 12, p. 2336-9 4 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  49. Acetaminophen and pregnancy: short- and long-term consequences for mother and child

    Thiele, K., Kessler, T., Arck, P., Erhardt, A. & Tiegs, G., 01.03.2013, In: J REPROD IMMUNOL. 97, 1, p. 128-39 12 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  50. A very rare cancer in Down Syndrome: medulloblastoma. Epidemiological data from 13 countries

    Satgé, D., Stiller, C. A., Rutkowski, S., von Bueren, A. O., Lacour, B., Sommelet, D., Nishi, M., Massimino, M., Garré, M. L., Moreno, F., Hasle, H., Jakab, Z., Greenberg, M., von der Weid, N., Kuehni, C., Zurriaga, O., Vicente, M-L., Peris-Bonet, R., Benesch, M., Vekemans, M., Sullivan, S. G. & Rickert, C., 01.03.2013, In: J NEURO-ONCOL. 112, 1, p. 107-14 8 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

  51. Cytokine concentrations and regulatory T cells in living donor and deceased donor liver transplant recipients

    Briem-Richter, A., Leuschner, A., Haag, F., Grabhorn, E. & Ganschow, R., 01.03.2013, In: PEDIATR TRANSPLANT. 17, 2, p. 185-90 6 p.

    Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review

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