Schmidt, F; Koch, R; Günther, O et al.
Mikrophthalmie, Hautanhangsgebilde und zerebrale Veränderungen.Monatsschr Kinderheilkd. Bd. 157. 2009 S. 418-421
Jones, SA; Almássy, Z; Beck, M et al.
Mortality and cause of death in mucopolysaccharidosis type II-a historical review based on data from the Hunter Outcome Survey (HOS)J Inherit Metab Dis. Bd. 32. H. 4. 2009 S. 534-43
Muenzer, J; Beck, M; Eng, CM et al.
Multidisciplinary management of Hunter syndromeJ Pediatr. Bd. 124. H. 6. 2009 S. e1228-39
Knuf, M; Faber, J; Habermehl, P
Nach Pertussisimpfung nur unzureichender NestschutzPädiat Prax. Bd. 74. H. 2. 2009 S. 331-36
Mehta, A; Clarke, JTR; Giugliani, R et al.
Natural course of Fabry disease: changing pattern of causes of death in FOS - Fabry Outcome SurveyJOURNAL OF MEDICAL GENETICS. Bd. 46. H. 8. 2009 S. 548-U63
Srokowski, CC; Masri, J; Hövelmeyer, N et al.
Naturally occurring short splice variant of CYLD positively regulates dendritic cell functionBlood. Bd. 113. H. 23. 2009 S. 5891-5
Marandiuc, D; Carbol, A; Runkel, S et al.
Neonatal alloimmune thrombocytopia caused by maternal low-affinity anti-HPA-1a antibody [Abstract]TRANSFUS MED HEMOTHER. Bd. 36. H. Spl. 2009 S. 56
Böckelmann, S; Marandiuc, D; Hitzler, W et al.
Neonatale Alloimmunthombopenie-schwierige Diagnose trotz eindeutiger Klinik [Abstract]MONATSSCHRIFT KINDERHEILKUNDE. Bd. 157. H. Spl. 2009 S. 22-23
Beetz, R
NephrologieZepp F, Wirth S (Hrsg). Handbuch Pädiatrie. Heidelberg: Springer Medizin Verlag 2009
Schermuly, I; Muller, MJ; Keller, I et al.
Neuropsychiatric symptoms, disease burden and brain structure in patients with Fabry diseaseINTERNATIONAL JOURNAL OF CLINICAL PHARMACOLOGY AND THERAPEUTICS. Bd. 47. 2009 S. S141-S141