Center for Obstetrics and Pediatrics

Publications

  1. 2012
  2. Approach to the management of slipped capital femoral epiphysis and primary hyperparathyroidism

    El Scheich, T., Marquard, J., Westhoff, B., Schneider, A., Cupisti, K., Oh, J., Meissner, T., Mayatepek, E. & Klee, D., 2012, In: J PEDIATR ENDOCR MET. 25, 3-4, p. 239-44 6 p.

    Research output: SCORING: Contribution to journalSCORING: Review articleResearch

  3. A prospective evaluation of degranulation assays in the rapid diagnosis of familial hemophagocytic syndromes.

    Bryceson, Y. T., Pende, D., Maul-Pavicic, A., Gilmour, K. C., Ufheil, H., Vraetz, T., Chiang, S. C., Marcenaro, S., Meazza, R., Bondzio, I., Walshe, D., Janka-Schaub, G., Lehmberg, K., Beutel, K., Zur Stadt, U., Binder, N., Arico, M., Moretta, L., Henter, J-I. & Ehl, S., 2012, In: BLOOD. 119, 12, p. 2754-2763 12.

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

  4. Association of shank 1A scaffolding protein with cone photoreceptor terminals in the mammalian retina.

    Stella, S. L., Vila, A., Hung, A. Y., Rome, M. E., Huynh, U., Sheng, M., Kreienkamp, H-J. & Brecha, N. C., 2012, In: PLOS ONE. 7, 9, p. 43463 9.

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

  5. Bioluminescence resonance energy Transfer: an emerging tool for the detection of protein-protein interaction in living cells

    Gersting, S. W., Lotz-Havla, A. S. & Muntau, A. C., 2012, In: Methods Mol Biol. 815, p. 253-63 11 p.

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

  6. Candidiasis caused by Candida kefyr in a neonate: case report.

    Weichert, S., Reinshagen, K., Zahn, K., Geginat, G., Dietz, A., Kilian, A. K., Schroten, H. & Tenenbaum, T., 2012, In: BMC INFECT DIS. 12, p. 61

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

  7. Cardiac MRI of the fetal heart using a novel triggering method: initial results in an animal model.

    Yamamura, J., Kopp, I., Frisch, M., Fischer, R., Valett, K., Hecher, K., Adam, G. & Wedegärtner, U., 2012, In: J MAGN RESON IMAGING. 35, 5, p. 1071-1076 5.

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

  8. Caspofungin as antifungal prophylaxis in pediatric patients undergoing allogeneic hematopoietic stem cell transplantation: a retrospective analysis.

    Döring, M., Hartmann, U., Erbacher, A., Lang, P., Handgretinger, R. & Müller, I., 2012, In: BMC INFECT DIS. 12, p. 151

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

  9. Clinical utility gene card for: adrenoleukodystrophy.

    Krasemann, E., Kemp, S. & Gal, A., 2012, In: EUR J HUM GENET. 20, 3, 3.

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

  10. Clinical utility gene card for: Fabry disease.

    Gal, A., Beck, M. & Winchester, B., 2012, In: EUR J HUM GENET. 20, 2, 2.

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

  11. Clinical utility gene card for: mucopolysaccharidosis type II.

    Beck, M., Wijburg, F. A. & Gal, A., 2012, In: EUR J HUM GENET. 20, 1, 1.

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

  12. Clinical utility gene card for: Werner syndrome.

    Hisama, F. M., Kubisch, C., Martin, G. M. & Oshima, J., 2012, In: EUR J HUM GENET. 20, 5, 5.

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

  13. Closing the case of APOE in multiple sclerosis: no association with disease risk in over 29 000 subjects.

    Lill, C. M., Liu, T., Schjeide, B-M. M., Roehr, J. T., Akkad, D. A., Damotte, V., Alcina, A., Ortiz, M. A., Arroyo, R., Aitzkoa, L. D. L., Blaschke, P., Winkelmann, A., Gerdes, L-A., Luessi, F., Fernadez, O., Izquierdo, G., Antigüedad, A., Hoffjan, S., Cournu-Rebeix, I., Gromöller, S., Faber, H., Liebsch, M., Meissner, E., Chanvillard, C., Touze, E., Pico, F., Corcia, P., Dörner, T., Steinhagen-Thiessen, E., Baeckman, L., Heekeren, H. R., Li, S-C., Lindenberger, U., Chan, A., Hartung, H-P., Aktas, O., Lohse, P., Kümpfel, T., Kubisch, C., Zettl, U. K., Fontaine, B., Vandenbroeck, K., Matesanz, F., Urcelay, E., Bertram, L. & Zipp, F., 2012, In: J MED GENET. 49, 9, p. 558-562 9.

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

  14. CNS PNET molecular subgroups with distinct clinical features.

    von Bueren, A. & André, O., 2012, In: LANCET ONCOL. 13, 8, p. 753-754 8.

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

  15. Comorbidities in chronic pediatric peritoneal dialysis patients: a report of the International Pediatric Peritoneal Dialysis Network

    Neu, A. M., Sander, A., Borzych-Duzalka, D., Watson, A. R., Vallés, P. G., Ha, I. S., Patel, H., Askenazi, D., Balasz-Chmielewska, I., Lauronen, J., Groothoff, J. W., Feber, J., Schaefer, F., Warady, B. A., IPPN investigators & Kemper, M. J., 2012, In: PERITON DIALYSIS INT. 32, 4, p. 410-8 9 p.

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

  16. Complementary dietary treatment using lysine-free, arginine-fortified amino acid supplements in glutaric aciduria type I - A decade of experience.

    Kölker, S., Boy, S. P. N., Heringer, J., Müller, E., Maier, E. M., Ensenauer, R., Mühlhausen, C., Schlune, A., Greenberg, C. R., Koeller, D. M., Hoffmann, G. F., Haege, G. & Burgard, P., 2012, In: MOL GENET METAB. 107, 1-2, p. 72-80 1-2.

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

  17. 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

  18. Defects in Transport: Mucolipidosis II alpha/beta, mucolipidosis III alpha/beta and mucolipidosis III gamma

    Raas-Rothschild, A., Pohl, S. & Braulke, T., 2012, Lysosomal Storage Disorders: A Practical Guide. WileyBlackwell, London, p. 121-126 6 p.

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

  19. Defibrotide for prophylaxis of hepatic veno-occlusive disease in paediatric haemopoietic stem-cell transplantation: an open-label, phase 3, randomised controlled trial.

    Corbacioglu, S., Cesaro, S., Faraci, M., Valteau-Couanet, D., Gruhn, B., Rovelli, A., Boelens, J. J., Hewitt, A., Schrum, J., Schulz, A. S., Müller, I., Stein, J., Wynn, R., Greil, J., Sykora, K-W., Matthes-Martin, S., Führer, M., O'Meara, A., Toporski, J., Sedlacek, P., Schlegel, P. G., Ehlert, K., Fasth, A., Winiarski, J., Arvidson, J., Mauz-Körholz, C., Ozsahin, H., Schrauder, A., Bader, P., Massaro, J., D'Agostino, R., Hoyle, M., Iacobelli, M., Debatin, K-M., Peters, C. & Dini, G., 2012, In: LANCET. 379, 9823, p. 1301-1309 9823.

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

  20. Deficiency for the ubiquitin ligase UBE3B in a blepharophimosis-ptosis-intellectual-disability syndrome.

    Basel-Vanagaite, L., Dallapiccola, B., Ramirez-Solis, R., Segref, A., Thiele, H., Edwards, A., Arends, M. J., Miró, X., White, J. K., Désir, J., Abramowicz, M., Dentici, M. L., Lepri, F., Hofmann, K., Har-Zahav, A., Ryder, E., Karp, N. A., Estabel, J., Gerdin, A-K. B., Podrini, C., Ingham, N. J., Altmüller, J., Nürnberg, G., Frommolt, P., Abdelhak, S., Pasmanik-Chor, M., Konen, O., Kelley, R. I., Shohat, M., Nürnberg, P., Flint, J., Steel, K. P., Hoppe, T., Kubisch, C., Adams, D. J. & Borck, G., 2012, In: AM J HUM GENET. 91, 6, p. 998-1010 6.

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

  21. Deletions in PITX1 cause a spectrum of lower-limb malformations including mirror-image polydactyly.

    Klopocki, E., Kähler, C., Foulds, N., Shah, H., Joseph, B., Vogel, H., Lüttgen, S., Bald, R., Besoke, R., Held, K., Mundlos, S. & Kurth, I., 2012, In: EUR J HUM GENET. 20, 6, p. 705-708 6.

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

  22. Dendritic mRNA targeting and translation.

    Kindler, S. & Kreienkamp, H-J., 2012, In: ADV EXP MED BIOL. 970, p. 285-305

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

  23. De novo germline and postzygotic mutations in AKT3, PIK3R2 and PIK3CA cause a spectrum of related megalencephaly syndromes.

    Rivière, J-B., Mirzaa, G. M., O'Roak, B. J., Beddaoui, M., Alcantara, D., Conway, R. L., St-Onge, J., Schwartzentruber, J. A., Gripp, K. W., Nikkel, S. M., Worthylake, T., Sullivan, C. T., Ward, T. R., Butler, H. E., Kramer, N. A., Albrecht, B., Armour, C. M., Armstrong, L., Caluseriu, O., Cytrynbaum, C., Drolet, B. A., Innes, A. M., Lauzon, J. L., Lin, A. E., Mancini, G. M. S., Meschino, W. S., Reggin, J. D., Saggar, A. K., Lerman-Sagie, T., Uyanik, G., Weksberg, R., Zirn, B., Beaulieu, C. L., Consortium, F. O. R. D. G. C., Majewski, J., Bulman, D. E., O'Driscoll, M., Shendure, J., Graham, J. M., Boycott, K. M. & Dobyns, W. B., 2012, In: NAT GENET. 44, 8, p. 934-940 8.

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

  24. Developmental programming of allergic diseases.

    Pincus, M. & Arck, P., 2012, In: Chem Immunol Allergy. 98, p. 70-84

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

  25. Disruption of the autophagy-lysosome pathway is involved in neuropathology of the nclf mouse model of neuronal ceroid lipofuscinosis.

    Thelen, M., Damme, M., Daμμe, M., Schweizer, M., Hagel, C., Wong, A. M. S., Cooper, J. D., Braulke, T. & Galliciotti, G., 2012, In: PLOS ONE. 7, 4, p. 35493 4.

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

  26. Dissecting the genomic complexity underlying medulloblastoma.

    Jones, D. T. W., Jäger, N., Kool, M., Zichner, T., Hutter, B., Sultan, M., Cho, Y-J., Pugh, T. J., Hovestadt, V., Stütz, A. M., Rausch, T., Warnatz, H-J., Ryzhova, M., Bender, S., Sturm, D., Pleier, S., Cin, H., Pfaff, E., Sieber, L., Wittmann, A., Remke, M., Witt, H., Hutter, S., Tzaridis, T., Weischenfeldt, J., Raeder, B., Avci, M., Amstislavskiy, V., Zapatka, M., Weber, U. D., Wang, Q., Lasitschka, B., Bartholomae, C. C., Schmidt, M., von Kalle, C., Ast, V., Lawerenz, C., Eils, J., Kabbe, R., Benes, V., van Sluis, P., Koster, J., Volckmann, R., Shih, D., Betts, M. J., Russell, R. B., Coco, S., Tonini, G. P., Schüller, U., Hans, V., Graf, N., Kim, Y-J., Monoranu, C., Roggendorf, W., Unterberg, A., Herold-Mende, C., Milde, T., Kulozik, A. E., von Deimling, A., Witt, O., Maass, E., Rössler, J., Ebinger, M., Schuhmann, M. U., Frühwald, M. C., Hasselblatt, M., Jabado, N., Rutkowski, S., von Bueren, A., André, O., Williamson, D., Clifford, S. C., McCabe, M. G., Collins, V. P., Wolf, S., Wiemann, S., Lehrach, H., Brors, B., Scheurlen, W., Felsberg, J., Reifenberger, G., Northcott, P. A., Taylor, M. D., Meyerson, M., Pomeroy, S. L., Yaspo, M-L., Korbel, J. O., Korshunov, A., Eils, R., Pfister, S. M. & Lichter, P., 2012, In: NATURE. 488, 7409, p. 100-105 7409.

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

  27. DNA copy number alterations in central primitive neuroectodermal tumors and tumors of the pineal region: an international individual patient data meta-analysis.

    von Bueren, A., André, O., Hagel, C., Hagel, C., Cai, H., Remke, M., Hasselblatt, M., Feuerstein, B. G., Pernet, S., Delattre, O., Rutkowski, S., Rutkowski, S., Pfister, S. M. & Baudis, M., 2012, In: J NEURO-ONCOL. 109, 2, p. 415-423 2.

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

  28. Duchenne muscular dystrophy in a 4-year-old girl due to heterozygous frame shift deletion of the dystrophin gene and skewed X-inactivation.

    Schänzer, A., Rau, I., Kress, W., Köhler, A., Neubauer, B. & Hahn, A., 2012, In: KLIN PADIATR. 224, 4, p. 256-258 4.

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

  29. DWI of the brain: postmortal DWI of the brain in comparison with in vivo data.

    Schmidt, T. M., Fischer, R., Acar, S., Lorenzen, M., Heinemann, A., Wedegärtner, U., Adam, G. & Yamamura, J., 2012, In: FORENSIC SCI INT. 220, 1-3, p. 180-183 1-3.

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

  30. Dysregulation of Rho GTPases in the αPix/Arhgef6 mouse model of X-linked intellectual disability is paralleled by impaired structural and synaptic plasticity and cognitive deficits.

    Ramakers, G. J. A., Wolfer, D., Rosenberger, G., Kuchenbecker, K., Kreienkamp, H-J., Prange-Kiel, J., Rune, G. M., Richter, K., Langnaese, K., Masneuf, S., Bösl, M. R., Fischer, K-D., Krugers, H. J., Lipp, H-P., van Galen, E. & Kutsche, K., 2012, In: HUM MOL GENET. 21, 2, p. 268-286 2.

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

  31. eIF2γ mutation that disrupts eIF2 complex integrity links intellectual disability to impaired translation initiation.

    Borck, G., Shin, B-S., Stiller, B., Mimouni-Bloch, A., Thiele, H., Kim, J-R., Thakur, M., Skinner, C., Aschenbach, L., Smirin-Yosef, P., Har-Zahav, A., Nürnberg, G., Altmüller, J., Frommolt, P., Hofmann, K., Konen, O., Nürnberg, P., Munnich, A., Schwartz, C. E., Gothelf, D., Colleaux, L., Dever, T. E., Kubisch, C. & Basel-Vanagaite, L., 2012, In: MOL CELL. 48, 4, p. 641-646 4.

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

  32. Elevated serum levels of B-cell activating factor in pediatric renal transplant patients.

    Lehnhardt, A., Dunst, F., Van Husen, M., Loos, S., Oh, J., Eiermann, T., Koch, M. & Kemper, M. J., 2012, In: PEDIATR NEPHROL. 27, 8, p. 1389-1395 8.

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

  33. Eradication of pulmonary aspergillosis in an adolescent patient undergoing three allogeneic stem cell transplantations for acute lymphoblastic leukemia.

    Döring, M., Zierl, A., Mezger, M., Lang, P., Handgretinger, R. & Müller, I., 2012, In: Case Rep Transplant. 2012, p. 672923

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

  34. Ertrinkungsunfall eines Kleinkinds im Gartenteich

    Singer, D., 2012, In: Notfallmedizin up2date. 7, p. 9-13

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

  35. Expert recommendations for the laboratory diagnosis of MPS VI.

    Wood, T., Bodamer, O. A., Burin, M. G., D'Almeida, V., Fietz, M., Giugliani, R., Hawley, S. M., Hendriksz, C. J., Hwu, W. L., Ketteridge, D., Lukacs, Z., Mendelsohn, N. J., Miller, N., Pasquali, M., Schenone, A., Schoonderwoerd, K., Winchester, B. & Harmatz, P., 2012, In: MOL GENET METAB. 106, 1, p. 73-82 1.

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

  36. Exploring the unique N-glycome of the opportunistic human pathogen Acanthamoeba.

    Schiller, B., Makrypidi, G., Razzazi-Fazeli, E., Paschinger, K., Walochnik, J. & Wilson, I. B. H., 2012, In: J BIOL CHEM. 287, 52, p. 43191-43204 52.

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

  37. Familial and acquired hemophagocytic lymphohistiocytosis.

    Janka-Schaub, G., 2012, In: ANNU REV MED. 63, p. 233-246

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

  38. Fatal EBV infection and variable clinical manifestations in an XLP-1 pedigree - rapid diagnosis of primary immunodeficiencies may save lives.

    Sperl, D., Benesch, M., Urban, C., Lackner, H., Sovinz, P., Speicher, M. R., Uhrig, S., Schwarzbraun, T., Schwinger, W., Zur Stadt, U., Beutel, K., Janka-Schaub, G., Scarpatetti, M. & Seidel, M. G., 2012, In: KLIN PADIATR. 224, 6, p. 386-389 6.

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

  39. Fetal Spleen

    Diemert, A. & Tutschek, B., 2012, Obstetric Imaging: Expert Radiology series. Saunders, p. 167-173 7 p.

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

  40. Fetoscopic management of gastroschisis in a lamb model.

    Bergholz, R., Krebs, T., Wenke, K., Andreas, T., Tiemann, B., Paetzel, J., Jacobsen, B., Fahje, R., Schmitz, C., Mann, O., Roth, B., Appl, B. & Hecher, K., 2012, In: SURG ENDOSC. 26, 5, p. 1412-1416 5.

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

  41. Fibroblast growth factor 23 and calcium phosphate homeostasis after pediatric renal transplantation.

    Van Husen, M., Lehnhardt, A., Fischer, A-K., Brinkert, F., Loos, S., Oh, J. & Kemper, M. J., 2012, In: PEDIATR TRANSPLANT. 16, 5, p. 443-450 5.

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

  42. Genome-wide association analysis identifies susceptibility loci for migraine without aura.

    Freilinger, T., Anttila, V., de Vries, B., Malik, R., Kallela, M., Terwindt, G. M., Pozo-Rosich, P., Winsvold, B., Nyholt, D. R., Oosterhout, V., Willebrordus, P. J., Artto, V., Todt, U., Hämäläinen, E., Fernández-Morales, J., Louter, M. A., Kaunisto, M. A., Schoenen, J., Raitakari, O., Lehtimäki, T., Vila-Pueyo, M., Göbel, H., Wichmann, E., Sintas, C., Uitterlinden, A. G., Hofman, A., Rivadeneira, F., Heinze, A., Tronvik, E., Duijn, V., Cornelia, M., Kaprio, J., Cormand, B., Wessman, M., Frants, R. R., Meitinger, T., Müller-Myhsok, B., Zwart, J-A., Färkkilä, M., Kubisch, C., Ferrari, M. D., Palotie, A., Dichgans, M., Maagdenberg, V. D., Arn, M. J. M. & Consortium, I. H. G., 2012, In: NAT GENET. 44, 7, p. 777-782 7.

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

  43. Gesundheitsbezogene Lebensqualität und psychische Gesundheit von kleinwüchsigen Kindern und Jugendlichen

    Quitman, J. H., Behncke, J., Dörr, H-G., Rolf, P. W., Wüsthof, A., Stahnke, N., Jakisch, B., Partsch, C-J., Nöker, M., Kuhnle-Krahl, U., Rohenkohl, A. C. & Bullinger, M., 2012, In: Z Med Psychol. 31, 3, p. 132-139 3.

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

  44. Glaucoma and frequency of ocular and general diseases in 30 patients with aniridia: a clinical study

    Gramer, E., Reiter, C. & Gramer, G., 2012, In: EUR J OPHTHALMOL. 22, 1, p. 104-10 7 p.

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

  45. Glyceroluria and neonatal hemochromatosis.

    Barić, I., Zibar, K., Ćorić, M., Santer, R., Bonilla, S., Bilić, K., Buljević, A. D., Benjak, V., Fumić, K. & Whitington, P. F., 2012, In: J PEDIATR GASTR NUTR. 55, 4, p. 126-128 4.

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

  46. Hepatocyte transplantation using the domino concept in a child with tetrabiopterin nonresponsive phenylketonuria

    Stéphenne, X., Debray, F. G., Smets, F., Jazouli, N., Sana, G., Tondreau, T., Menten, R., Goffette, P., Boemer, F., Schoos, R., Gersting, S. W., Najimi, M., Muntau, A. C., Goyens, P. & Sokal, E. M., 2012, In: CELL TRANSPLANT. 21, 12, p. 2765-70 6 p.

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

  47. [Hereditary cardiac amyloidosis with transthyretin mutations. A cause of sudden death ].

    Edler, C., Saeger, W., Orth, U., Braun, C., Wulff, B. & Sperhake, J., 2012, In: HERZ. 37, 4, p. 456-460 4.

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

  48. High expression of disease-related Cln6 in the cerebral cortex, purkinje cells, dentate gyrus, and hippocampal ca1 neurons.

    Thelen, M., Fehr, S., Schweizer, M., Braulke, T. & Galliciotti, G., 2012, In: J NEUROSCI RES. 90, 3, p. 568-574 3.

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

  49. High serum adiponectin concentration in children with chronic kidney disease.

    Möller, K., Dieterman, C., Herich, L., Klaassen, I., Kemper, M. J. & Müller-Wiefel, D. E., 2012, In: PEDIATR NEPHROL. 27, 2, p. 243-249 2.

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

  50. Hyperfractionated versus conventional radiotherapy followed by chemotherapy in standard-risk medulloblastoma: results from the randomized multicenter HIT-SIOP PNET 4 trial.

    Lannering, B., Rutkowski, S., Doz, F., Pizer, B., Gustafsson, G., Navajas, A., Massimino, M., Reddingius, R., Benesch, M., Carrie, C., Taylor, R., Gandola, L., Björk-Eriksson, T., Giralt, J., Oldenburger, F., Pietsch, T., Figarella-Branger, D., Robson, K., Forni, M., Clifford, S. C., Warmuth-Metz, M., von Hoff, K., Faldum, A., Mosseri, V. & Kortmann, R., 2012, In: J CLIN ONCOL. 30, 26, p. 3187-3193 26.

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

  51. Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia.

    Ellinghaus, E., Stanulla, M., Richter, G., Ellinghaus, D., Te Kronnie, G., Cario, G., Cazzaniga, G., Horstmann, M., Panzer Grümayer, R., Cavé, H., Trka, J., Cinek, O., Teigler-Schlegel, A., ElSharawy, A., Häsler, R., Nebel, A., Meissner, B., Bartram, T., Lescai, F., Franceschi, C., Giordan, M., Nürnberg, P., Heinzow, B., Zimmermann, M., Schreiber, S., Schrappe, M. & Franke, A., 2012, In: LEUKEMIA. 26, 5, p. 902-909 5.

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