Ramaswami, U; Whybra, C; Kalkum, G et al.
Measuring patient experiences in fabry disease: validation of the Fabry Outcome Survey (FOS) paediatric health and pain questionnaireMOLECULAR GENETICS AND METABOLISM. Bd. 102. H. 2. 2011 S. S37-S38
Mildenberger, E
Mekoniumaspiration [Abstract]. Gesellschaft für Neonatologie und Pädiatrische Intensivmedizin, Mannheim, 2011Monatsschr Kinderheilkd. Bd. 159. H. Spl2. 2011 S. 36
Zepp, F; Hoffmann, GF
Metabolism and Gene DiagnosticsMONATSSCHRIFT KINDERHEILKUNDE. Bd. 159. H. 9. 2011 S. 813-813
Kantor, C; Panaitescu, B; Kuribayashi, J et al.
Methylxanthine-evoked seizure-like pertubation of isolated newborn rat hippocampal and cortical networks [Abstract]FASEB J. Bd. 25. H. 1b. 2011 S. 522
Bernt, KM; Zhu, N; Sinha, AU et al.
MLL-Rearranged Leukemia Is Dependent on Aberrant H3K79 Methylation by DOT1LCANCER CELL. Bd. 20. H. 1. 2011 S. 66-78
Staatz, G; Zepp, F
Modern imaging in child and adolescent medicineMONATSSCHRIFT KINDERHEILKUNDE. Bd. 159. H. 4. 2011 S. 317-318
Beck, M
Mucopolysaccharidosis Type II (Hunter Syndrome): Clinical Picture and TreatmentCURRENT PHARMACEUTICAL BIOTECHNOLOGY. Bd. 12. H. 6. 2011 S. 861-866
Scarpa, M; Almassy, Z; Beck, M et al.
Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare diseaseORPHANET JOURNAL OF RARE DISEASES. Bd. 6. 2011 S. -
Weber, S; Thiele, H; Mir, S et al.
Muscarinic Acetylcholine Receptor M3 Mutation Causes Urinary Bladder Disease and a Prune-Belly-like SyndromeAMERICAN JOURNAL OF HUMAN GENETICS. Bd. 89. H. 5. 2011 S. 668-674
Wirth, S; Zepp, F
Musculoeskeletal DisordersMONATSSCHRIFT KINDERHEILKUNDE. Bd. 159. H. 1. 2011 S. 16-16