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A case of combined Farber and Sandhoff disease.
Fusch C, Huenges R, Moser HW, Sewell AC, Roggendorf W, Kustermann-Kuhn B, Poulos A, Carey WF, Harzer K. Fusch C, et al. Among authors: harzer k. Eur J Pediatr. 1989 Apr;148(6):558-62. doi: 10.1007/BF00441558. Eur J Pediatr. 1989. PMID: 2744019
B1 variant of GM2 gangliosidosis in a 12-year-old patient.
Goebel HH, Stolte G, Kustermann-Kuhn B, Harzer K. Goebel HH, et al. Among authors: harzer k. Pediatr Res. 1989 Jan;25(1):89-93. doi: 10.1203/00006450-198901000-00019. Pediatr Res. 1989. PMID: 2521932
Leptomeningeal lipid storage patterns in Fabry disease.
Elleder M, Christomanou H, Kustermann-Kuhn B, Harzer K. Elleder M, et al. Among authors: harzer k. Acta Neuropathol. 1994;88(6):579-82. doi: 10.1007/BF00296496. Acta Neuropathol. 1994. PMID: 7879606
161 results