Department of Pediatrics

Publications

  1. 2019
  2. Phenotype in an Infant with SOD1 Homozygous Truncating Mutation

    Andersen, P. M., Nordström, U., Tsiakas, K., Johannsen, J., Volk, A. E., Bierhals, T., Zetterström, P., Marklund, S. L., Hempel, M. & Santer, R., 01.08.2019, In: NEW ENGL J MED. 381, 5, p. 486-488 3 p.

    Research output: SCORING: Contribution to journalOther (editorial matter etc.)Research

  3. Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patients

    Renner, S., Schüler, H., Alawi, M., Kolbe, V., Rybczynski, M., Woitschach, R., Sheikhzadeh, S., Stark, V. C., Olfe, J., Roser, E., Seggewies, F. S., Mahlmann, A., Hempel, M., Hartmann, M. J., Hillebrand, M., Wieczorek, D., Volk, A. E., Kloth, K., Koch-Hogrebe, M., Abou Jamra, R., Mitter, D., Altmüller, J., Wey-Fabrizius, A., Petersen, C., Rau, I., Borck, G., Kubisch, C., Mir, T. S., von Kodolitsch, Y., Kutsche, K. & Rosenberger, G., 08.2019, In: GENET MED. 21, 8, p. 1832-1841 10 p.

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

  4. Zufallsbefund: Milchiges Blut bei einem jungen Säugling

    Kohl, A. P., Blohm, M. E., Schmitt, C. & Singer, D., 08.2019, In: Z GEBURTSH NEONATOL. 223, 4, p. 249-250 2 p.

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearch

  5. Clinical burden of illness in patients with phenylketonuria (PKU) and associated comorbidities - a retrospective study of German health insurance claims data

    Trefz, K. F., Muntau, A. C., Kohlscheen, K. M., Altevers, J., Jacob, C., Braun, S., Greiner, W., Jha, A., Jain, M., Alvarez, I., Lane, P., Schröder, C. & Rutsch, F., 22.07.2019, In: ORPHANET J RARE DIS. 14, 1, p. 181

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

  6. Analysis of the caregiver burden associated with Sanfilippo syndrome type B: panel recommendations based on qualitative and quantitative data

    Shapiro, E., Lourenço, C. M., Mungan, N. O., Muschol, N., O'Neill, C. & Vijayaraghavan, S., 08.07.2019, In: ORPHANET J RARE DIS. 14, 1, p. 168

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

  7. The Genomics of Arthrogryposis, a Complex Trait: Candidate Genes and Further Evidence for Oligogenic Inheritance

    Pehlivan, D., Bayram, Y., Gunes, N., Coban Akdemir, Z., Shukla, A., Bierhals, T., Tabakci, B., Sahin, Y., Gezdirici, A., Fatih, J. M., Gulec, E. Y., Yesil, G., Punetha, J., Ocak, Z., Grochowski, C. M., Karaca, E., Albayrak, H. M., Radhakrishnan, P., Erdem, H. B., Sahin, I., Yildirim, T., Bayhan, I. A., Bursali, A., Elmas, M., Yuksel, Z., Ozdemir, O., Silan, F., Yildiz, O., Yesilbas, O., Isikay, S., Balta, B., Gu, S., Jhangiani, S. N., Doddapaneni, H., Hu, J., Muzny, D. M., Baylor Hopkins Center for Mendelian Genomics, Boerwinkle, E., Gibbs, R. A., Tsiakas, K., Hempel, M., Girisha, K. M., Gul, D., Posey, J. E., Elcioglu, N. H., Tuysuz, B. & Lupski, J. R., 03.07.2019, In: AM J HUM GENET. 105, 1, p. 132-150 19 p.

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

  8. Clostridium difficile infection after pediatric solid organ transplantation: a practical single-center experience

    Breuer, C., Döring, S., Rohde, H., Rutkowski, S., Müller, I. & Oh, J., 07.2019, In: PEDIATR NEPHROL. 34, 7, p. 1269-1275 7 p.

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

  9. Ketogenic diet ameliorates axonal defects and promotes myelination in Pelizaeus-Merzbacher disease

    Stumpf, S. K., Berghoff, S. A., Trevisiol, A., Spieth, L., Düking, T., Schneider, L. V., Schlaphoff, L., Dreha-Kulaczewski, S., Bley, A., Burfeind, D., Kusch, K., Mitkovski, M., Ruhwedel, T., Guder, P., Röhse, H., Denecke, J., Gärtner, J., Möbius, W., Nave, K-A. & Saher, G., 07.2019, In: ACTA NEUROPATHOL. 138, 1, p. 147-161 15 p.

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

  10. Low levels of urinary epidermal growth factor predict chronic kidney disease progression in children

    Azukaitis, K., Ju, W., Kirchner, M., Nair, V., Smith, M., Fang, Z., Thurn-Valsassina, D., Bayazit, A., Niemirska, A., Canpolat, N., Bulut, I. K., Yalcinkaya, F., Paripovic, D., Harambat, J., Cakar, N., Alpay, H., Lugani, F., Mencarelli, F., Civilibal, M., Erdogan, H., Gellermann, J., Vidal, E., Tabel, Y., Gimpel, C., Ertan, P., Yavascan, O., Melk, A., Querfeld, U., Wühl, E., Kretzler, M., Schaefer, F., 4C Study & ESCAPE Trial Group, 07.2019, In: KIDNEY INT. 96, 1, p. 214-221 8 p.

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

  11. Novel variants and clinical symptoms in four new ALG3-CDG patients, review of the literature, and identification of AAGRP-ALG3 as a novel ALG3 variant with alanine and glycine-rich N-terminus

    Himmelreich, N., Dimitrov, B., Geiger, V., Zielonka, M., Hutter, A-M., Beedgen, L., Hüllen, A., Breuer, M., Peters, V., Thiemann, K-C., Hoffmann, G. F., Sinning, I., Dupré, T., Vuillaumier-Barrot, S., Barrey, C., Denecke, J., Kölfen, W., Düker, G., Ganschow, R., Lentze, M. J., Moore, S., Seta, N., Ziegler, A. & Thiel, C., 07.2019, In: HUM MUTAT. 40, 7, p. 938-951 14 p.

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

  12. Reducing Hematologic Toxicity With Short Course Postexposure Prophylaxis With Zidovudine for HIV-1 Exposed Infants With Low Transmission Risk

    Nguyen, T. T. T., Kobbe, R., Schulze-Sturm, U., Blohm, M., Hollwitz, B., Hertling, S., Becker, C., Oommen, P. T., Laws, H-J., Martignoni, F., Ole Jensen, B-E., Olah, K., Schmidtke, S., Kreuels, B., Vasconcelos, M. K. & Neubert, J., 07.2019, In: PEDIATR INFECT DIS J. 38, 7, p. 727-730 4 p.

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

  13. The lysosomal storage disorders mucolipidosis type II, type III alpha/beta and type III gamma: Update on GNPTAB and GNPTG mutations

    Velho, R. V., Harms, F. L., Danyukova, T., Ludwig, N. F., Friez, M. J., Cathey, S. S., Filocamo, M., Tappino, B., Güneş, N., Tüysüz, B., Tylee, K. L., Brammeier, K. L., Heptinstall, L., Oussoren, E., van der Ploeg, A. T., Petersen, C., Alves, S., Saavedra, G. D., Schwartz, I. V., Muschol, N., Kutsche, K. & Pohl, S., 07.2019, In: HUM MUTAT. 40, 7, p. 842-864 23 p.

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

  14. Levamisole in Children with Idiopathic Nephrotic Syndrome: Clinical Efficacy and Pathophysiological Aspects

    Mühlig, A. K., Lee, J. Y., Kemper, M. J., Kronbichler, A., Yang, J. W., Lee, J. M., Shin, J. I. & Oh, J., 16.06.2019, In: J CLIN MED. 8, 6

    Research output: SCORING: Contribution to journalSCORING: Review articleResearch

  15. Acute dialysis in children: Results of a European Survey.

    Guzzo, I., de Galasso, L., Mir, S., Bulut, I. K., Jankauskiene, A., Burokiene, V., Cvetkovic, M., Kostic, M., Bayazit, A. K., Yildizdas, D., Schmitt, C. P., Paglialonga, F., Montini, G., Yilmaz, E., Oh, J., Weber, L., Taylan, C., Hayes, W., Shroff, R., Vidal, E., Murer, L., Mencarelli, F., Pasini, A., Teixeira, A., Afonso, A. C., Drozdz, D., Schaefer, F., Picca, S. & ESCAPE Network, 06.2019, In: J NEPHROL. 32, 3, p. 445-451 7 p.

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

  16. Biallelic variants in SMAD6 are associated with a complex cardiovascular phenotype

    Kloth, K., Bierhals, T., Johannsen, J., Harms, F. L., Juusola, J., Johnson, M. C., Grange, D. K. & Kutsche, K., 06.2019, In: HUM GENET. 138, 6, p. 625-634 10 p.

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

  17. Dorsal root ganglia volume is increased in patients with the Fabry-related GLA variant p.D313Y

    Godel, T., Bäumer, P., Stumpfe, K., Muschol, N., Kronlage, M., Brunnée, M., Kollmer, J., Heiland, S., Bendszus, M. & Mautner, V-F., 06.2019, In: J NEUROL. 266, 6, p. 1332-1339 8 p.

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

  18. Epidemiology of and Risk Factors for BK Polyomavirus Replication and Nephropathy in Pediatric Renal Transplant Recipients: An International CERTAIN Registry Study

    Höcker, B., Schneble, L., Murer, L., Carraro, A., Pape, L., Kranz, B., Oh, J., Zirngibl, M., Dello Strologo, L., Büscher, A., Weber, L. T., Awan, A., Pohl, M., Bald, M., Printza, N., Rusai, K., Peruzzi, L., Topaloglu, R., Fichtner, A., Krupka, K., Köster, L., Bruckner, T., Schnitzler, P., Hirsch, H. H. & Tönshoff, B., 06.2019, In: TRANSPLANTATION. 103, 6, p. 1224-1233 10 p.

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

  19. HNF1B nephropathy has a slow-progressive phenotype in childhood-with the exception of very early onset cases: results of the German Multicenter HNF1B Childhood Registry.

    Okorn, C., Goertz, A., Vester, U., Beck, B. B., Bergmann, C., Habbig, S., König, J., Konrad, M., Müller, D., Oh, J., Ortiz-Brüchle, N., Patzer, L., Schild, R., Seeman, T., Staude, H., Thumfart, J., Tönshoff, B., Walden, U., Weber, L., Zaniew, M., Zappel, H., Hoyer, P. F. & Weber, S., 06.2019, In: PEDIATR NEPHROL. 34, 6, p. 1065-1075 11 p.

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

  20. Patient reported outcomes in Friedreich's Ataxia after withdrawal from Idebenone

    Cook, A., Boesch, S., Heck, S., Brunt, E., Klockgether, T., Schöls, L., Schulz, A. & Giunti, P., 06.2019, In: ACTA NEUROL SCAND. 139, 6, p. 533-539 7 p.

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

  21. Growth charts for patients with Sanfilippo syndrome (Mucopolysaccharidosis type III)

    Muschol, N. M., Pape, D., Kossow, K., Ullrich, K., Arash-Kaps, L., Hennermann, J. B., Stücker, R. & Breyer, S., 02.05.2019, In: ORPHANET J RARE DIS. 14, 1, p. 93

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

  22. Cerebrospinal fluid biogenic amines depletion and brain atrophy in adult patients with phenylketonuria

    Pilotto, A., Blau, N., Leks, E., Schulte, C., Deuschl, C., Zipser, C., Piel, D., Freisinger, P., Gramer, G., Kölker, S., Haas, D., Burgard, P., Nawroth, P., Georg, H., Scheffler, K., Berg, D. & Trefz, F., 05.2019, In: J INHERIT METAB DIS. 42, 3, p. 398-406 9 p.

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

  23. International best practice for the evaluation of responsiveness to sapropterin dihydrochloride in patients with phenylketonuria

    Muntau, A. C., Adams, D. J., Bélanger-Quintana, A., Bushueva, T. V., Cerone, R., Chien, Y-H., Chiesa, A., Coşkun, T., de Las Heras, J., Feillet, F., Katz, R., Lagler, F., Piazzon, F., Rohr, F., van Spronsen, F. J., Vargas, P., Wilcox, G. & Bhattacharya, K., 05.2019, In: MOL GENET METAB. 127, 1, p. 1-11 11 p.

    Research output: SCORING: Contribution to journalSCORING: Review articleResearch

  24. Nestin progenitor cells isolated from adult human sweat gland stroma promote reepithelialisation and may stimulate angiogenesis in wounded human skin ex vivo

    Liao, T., Lehmann, J., Sternstein, S., Yay, A., Zhang, G., Matthießen, A. E., Schumann, S., Siemers, F., Kruse, C., Hundt, J. E., Langan, E. A., Tiede, S. & Paus, R., 05.2019, In: ARCH DERMATOL RES. 311, 4, p. 325-330 6 p.

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

  25. Validity of a rapid and simple fluorometric tripeptidyl peptidase 1 (TPP1) assay using dried blood specimens to diagnose CLN2 disease

    Lukacs, Z., Nickel, M., Murko, S., Nieves Cobos, P., Schulz, A., Santer, R. & Kohlschütter, A., 05.2019, In: CLIN CHIM ACTA. 492, p. 69-71 3 p.

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

  26. Novel likely pathogenic variants in TMEM126A identified in non-syndromic autosomal recessive optic atrophy: two case reports

    Kloth, K., Synofzik, M., Kernstock, C., Schimpf-Linzenbold, S., Schuettauf, F., Neu, A., Wissinger, B. & Weisschuh, N., 08.04.2019, In: BMC MED GENET. 20, 1, p. 62

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

  27. Current and Emerging Treatment Strategies for Neuronal Ceroid Lipofuscinoses

    Kohlschütter, A., Schulz, A., Bartsch, U. & Storch, S., 04.2019, In: CNS DRUGS. 33, 4, p. 315-325 11 p.

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

  28. KAT6A Syndrome: genotype-phenotype correlation in 76 patients with pathogenic KAT6A variants

    Kennedy, J., Goudie, D., Blair, E., Chandler, K., Joss, S., McKay, V., Green, A., Armstrong, R., Lees, M., Kamien, B., Hopper, B., Tan, T. Y., Yap, P., Stark, Z., Okamoto, N., Miyake, N., Matsumoto, N., Macnamara, E., Murphy, J. L., McCormick, E., Hakonarson, H., Falk, M. J., Li, D., Blackburn, P., Klee, E., Babovic-Vuksanovic, D., Schelley, S., Hudgins, L., Kant, S., Isidor, B., Cogne, B., Bradbury, K., Williams, M., Patel, C., Heussler, H., Duff-Farrier, C., Lakeman, P., Scurr, I., Kini, U., Elting, M., Reijnders, M., Schuurs-Hoeijmakers, J., Wafik, M., Blomhoff, A., Ruivenkamp, C. A. L., Nibbeling, E., Dingemans, A. J. M., Douine, E. D., Nelson, S. F., DDD Study, Hempel, M., Bierhals, T., Lessel, D., Johannsen, J., Arboleda, V. A. & Newbury-Ecob, R., 04.2019, In: GENET MED. 21, 4, p. 850-860 11 p.

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

  29. Nanobody-targeting of epidermal growth factor receptor (EGFR) ectodomain variants overcomes resistance to therapeutic EGFR antibodies

    Tintelnot, J., Baum, N., Schultheiss, C., Braig, F., Trentmann, M., Finter, J., Fumey, W., Bannas, P., Fehse, B., Riecken, K., Schütze, K., Bokemeyer, C., Rösner, T., Valerius, T., Peipp, M., Koch-Nolte, F. & Binder, M., 04.2019, In: MOL CANCER THER. 18, 4, p. 823-833 11 p.

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

  30. Exome Sequencing in Children: Undiagnosed Developmental Delay and Neurological Illness

    Mahler, E. A., Johannsen, J., Tsiakas, K., Kloth, K., Lüttgen, S., Mühlhausen, C., Alhaddad, B., Haack, T. B., Strom, T. M., Kortüm, F., Meitinger, T., Muntau, A. C., Santer, R., Kubisch, C., Lessel, D., Denecke, J. & Hempel, M., 22.03.2019, In: DTSCH ARZTEBL INT. 116, 12, p. 197-204 8 p.

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

  31. Isoform-specific domain organization determines conformation and function of the peroxisomal biogenesis factor PEX26

    Guder, P., Lotz-Havla, A. S., Woidy, M., Reiß, D. D., Danecka, M. K., Schatz, U. A., Becker, M., Ensenauer, R., Pagel, P., Büttner, L., Muntau, A. C. & Gersting, S. W., 03.2019, In: BBA-MOL CELL RES. 1866, 3, p. 518-531 14 p.

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

  32. TANGO2: expanding the clinical phenotype and spectrum of pathogenic variants

    Dines, J. N., Golden-Grant, K., LaCroix, A., Muir, A. M., Cintrón, D. L., McWalter, K., Cho, M. T., Sun, A., Merritt, L., Thies, J., Niyazov, D., Burton, B., Kim, K., Fleming, L., Westman, R., Karachunski, P., Dalton, J., Basinger, A., Ficicioglu, C., Helbig, I., Pendziwiat, M., Muhle, H., Helbig, K. L., Caliebe, A., Santer, R., Becker, K., Suchy, S., Douglas, G., Millan, F., Begtrup, A., Monaghan, K. G. & Mefford, H. C., 03.2019, In: GENET MED. 21, 3, p. 601-607 7 p.

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

  33. The Contribution of Homocysteine Metabolism Disruption to Endothelial Dysfunction: State-of-the Art

    Esse, R., Barroso, M., Tavares de Almeida, I. & Castro, R., 17.02.2019, In: INT J MOL SCI. 20, 4

    Research output: SCORING: Contribution to journalSCORING: Review articleResearch

  34. A newly generated neuronal cell model of CLN7 disease reveals aberrant lysosome motility and impaired cell survival.

    von Kleist, L., Ariunbat, K., Braren, I., Stauber, T., Storch, S. & Danyukova, T., 02.2019, In: MOL GENET METAB. 126, 2, p. 196-205 10 p.

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

  35. Fatigue in pediatric liver transplant recipients and its impact on their quality of life

    Petersen, I., Noelle, J., Buchholz, A., Kroencke, S., Daseking, M. & Grabhorn, E., 02.2019, In: PEDIATR TRANSPLANT. 23, 1, p. e13331

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

  36. Influenza binds phosphorylated glycans from human lung

    Byrd-Leotis, L., Jia, N., Dutta, S., Trost, J. F., Gao, C., Cummings, S. F., Braulke, T., Müller-Loennies, S., Heimburg-Molinaro, J., Steinhauer, D. A. & Cummings, R. D., 02.2019, In: SCI ADV. 5, 2, eaav2554.

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

  37. Intrathecal heparan-N-sulfatase in patients with Sanfilippo syndrome type A: A phase IIb randomized trial

    Wijburg, F. A., Whitley, C. B., Muenzer, J., Gasperini, S., Del Toro, M., Muschol, N., Cleary, M., Sevin, C., Shapiro, E., Bhargava, P., Kerr, D. & Alexanderian, D., 02.2019, In: MOL GENET METAB. 126, 2, p. 121-130 10 p.

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

  38. A recurrent de-novo ANO3 mutation causes early-onset generalized dystonia

    Tunc, S., Denecke, J., Olschewski, L., Bäumer, T., Münchau, A., Lessel, D. & Lohmann, K., 15.01.2019, In: J NEUROL SCI. 396, p. 199-201 3 p.

    Research output: SCORING: Contribution to journalOther (editorial matter etc.)Research

  39. Clinical challenges and future therapeutic approaches for neuronal ceroid lipofuscinosis

    Mole, S. E., Anderson, G., Band, H. A., Berkovic, S. F., Cooper, J. D., Kleine Holthaus, S-M., McKay, T. R., Medina, D. L., Rahim, A. A., Schulz, A. & Smith, A. J., 01.2019, In: LANCET NEUROL. 18, 1, p. 107-116 10 p.

    Research output: SCORING: Contribution to journalSCORING: Review articleResearch

  40. Malaria in Eritrean migrants newly arrived in seven European countries, 2011 to 2016

    Sondén, K., Rolling, T., Wångdahl, A., Ydring, E., Vygen-Bonnet, S., Kobbe, R., Douhan, J., Hammar, U., Duijster, J., de Gier, B., Freedman, J., Gysin, N., Stark, K., Stevens, F., Vestergaard, L. S., Tegnell, A. & Färnert, A., 01.2019, In: EUROSURVEILLANCE. 24, 5

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

  41. Radiation exposure by digital radiographic imaging in very low birth weight infants

    Ebenebe, C. U., Barreau, C., Waschkewitz, J., Schlattl, H., Pinnschmidt, H. O., Deindl, P., Singer, D. & Herrmann, J., 01.2019, In: J PERINATOL. 39, 1, p. 115-119 5 p.

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

  42. Anpassungsstörungen des Neugeborenen

    Singer, D. & Deindl, P., 2019, Referenz Notfallmedizin. Scholz, J., Gräsner, J-T. & Bohn, A. (eds.). 1 ed. Stuttgart: Georg Thieme Verlag KG, p. 603-612 10 p.

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

  43. Clinical and Immunological Phenotype of Patients With Primary Immunodeficiency Due to Damaging Mutations in NFKB2

    Klemann, C., Camacho-Ordonez, N., Yang, L., Eskandarian, Z., Rojas-Restrepo, J. L., Frede, N., Bulashevska, A., Heeg, M., Al-Ddafari, M. S., Premm, J., Seidl, M., Ammann, S., Sherkat, R., Radhakrishnan, N., Warnatz, K., Unger, S., Kobbe, R., Hüfner, A., Leahy, T. R., Ip, W., Burns, S. O., Fliegauf, M. & Grimbacher, B., 2019, In: FRONT IMMUNOL. 10, p. 297

    Research output: SCORING: Contribution to journalSCORING: Journal articleResearch

  44. Frühzeitige Diagnose einer seltenen Krankheit bei Kindern durchbessere Kommunikation zwischen Eltern, niedergelassenen Ärztenund spezialisierten Zentren

    Kohlschütter, A. & Bussche van den, H., 2019, In: Z EVIDENZ FORTBILD Q. 2019, 141-142, p. 18-23

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

  45. Hibernating astronauts - science or fiction?

    Choukèr, A., Bereiter-Hahn, J., Singer, D. & Heldmaier, G., 2019, In: PFLUG ARCH EUR J PHY. 471, p. 819-828

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

  46. Kindesmisshandlung: interdisziplinärer Kinderschutz

    Seifert, D. & Ewert, J. N., 2019, In: Allgemein- und Viszeralchirurgie up2date. 2019, 13, p. 419 - 437

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

  47. Kindesmisshandlung: interdisziplinärer Kinderschutz.

    Seifert, D. & Ewert, J. N., 2019, In: ANASTH INTENSIV NOTF. 2019, 54, p. 1 - 20

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

  48. Neonatologie: Versuch einer Bestandsaufnahme

    Singer, D., 2019, In: Kinder- und Jugendarzt. 50, p. 319-327

    Research output: SCORING: Contribution to journalSCORING: Review articleTransfer

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