Queisser-Wahrendorf, A; Wiesel, A; Stolz, G
Aktuelle Daten aus dem Geburtenregister Mainzer Modell (MaMo) Fehlbildungen- Häufigkeiten und RisikofaktorenKinder- und Jugendarzt. Bd. 47.Jg. H. 6. 2016 S. ff
Willasch, A. M.; Salzmann, E.; Krenn, T. et al.
Algorithm for the treatment of relapse after allogeneic stem cell transplantation in children and adolescents with acute lymphoblastic leukemia: The Frankfurt experienceBONE MARROW TRANSPLANTATION. Bd. 51. 2016 S. S253-S254
Beetz, Rolf
Antibakterielle Prophylaxe von HarnwegsinfektionenKinder- und Jugendmedizin. Bd. 16. 2016 S. 349-358
Nestrasil, Igor; Wakumoto, Amy; Rudser, Kyle et al.
Brain MRI patterns in MPS IIIB (Sanfilippo syndrome type B): A longitudinal studyMOLECULAR GENETICS AND METABOLISM. Bd. 117. H. 2. 2016 S. S86-S86
Ramaswami, Uma; Beck, Michael; Hughes, Derralynn et al.
Cardio-renal outcomes with long-term agalsidase alfa enzyme replacement therapy: A 10-year Fabry Outcome Survey analysisMOLECULAR GENETICS AND METABOLISM. Bd. 117. H. 2. 2016 S. S98-S98
Imrie, Jackie; Mengel, Karl Eugen; Cassiman, David et al.
Cause of death in patients with attenuated acid sphingomyelinase deficiency: Comprehensive literature review and report of new casesMOLECULAR GENETICS AND METABOLISM. Bd. 117. H. 2. 2016 S. S60-S60
Cassiman, David; Packman, Seymour; Bembi, Bruno et al.
Cause of death in patients with chronic visceral and chronic neurovisceral acid sphingomyelinase deficiency (Niemann-Pick disease type B and B variant): Literature review and report of new casesMOLECULAR GENETICS AND METABOLISM. Bd. 118. H. 3. 2016 S. 206-213
Fischer, J*; Paret, C*; El Malki, K et al.
CD19 isoforms lacking the CART-19 epitope are expressed before any therapyJournal of Immunotherapy. 2016 S. ff
Schmeh, Isabella; Kidszun, Andre; Lausch, Ekkehart et al.
Chest Radiograph as Diagnostic Clue in a Floppy InfantJOURNAL OF PEDIATRICS. Bd. 177. 2016 S. 324-+
van Capelle, C. I.; van der Meijden, J. C.; van den Hout, J. M. P. et al.
Childhood Pompe disease: clinical spectrum and genotype in 31 patientsORPHANET JOURNAL OF RARE DISEASES. Bd. 11. 2016