PD Dr. Michael Beck - Publikationen

Barone, R.; Brühl, K.; Stoeter, P. et al.
Clinical and Neuroradiological Findings in Classic Infantile and Late-Onset Globoid-Cell Leukodystrophy (Krabbe Disease)
American journal of medical genetics. Bd. 63. H. 1. Hoboken, NJ: Wiley-Liss 1996 S. 209 - 217

Beck, M.; Barone, R.; Hoffmann, R. et al.
Inter- and intrafamilial variability in mucolipidosis II (I-cell disease)
Clinical genetics. an international journal of genetics in medicine. Bd. 47. H. 4. Oxford: Blackwell Munksgaard 1995 S. 191 - 199

Beck, M.; Spranger, J.; Fernandes, J. et al.
Mucopolysaccharides and Oligosaccharides
Fernandes, J.; Saudubray, J.M.; van den Berghe, G. (Hrsg). Inborn Metabolic Diseases. Berlin: Springer 1995 S. 383-388

Beck, M.; Valadares, E.R.; Lotz, J.
Gaucher's disease: therapy by intravenous infusions of modified glucocerebrosidase
The clinical investigator. official organ of the "Gesellschaft Deutscher Naturforscher und Ärzte". Bd. 71. H. 1. Berlin: Springer 1993

Steglich, C.; Zabel, B.; Dahl, N. et al.
Deletion of the Hunter Gene and both DXS466 and DXS304 in a Patient with Mucopolysaccharidosis Type II
Am. J. Med. Genet. Bd. Am. J. Med. Genet. 1992 S. 100-103