Funder
Deutsche Forschungsgemeinschaft
Subject
Genetics (clinical),Genetics
Reference31 articles.
1. Barkovich AJ, Peck WW (1997) MR of Zellweger syndrome. AJNR Am J Neuroradiol 18(6):1163–1170
2. Bowen P, Lee CS, Zellweger H, Lindenberg R (1964) A familial syndrome of multiple congenital defects. Bull Johns Hopkins Hosp 114:402–414
3. Bruhn H, Kruse B, Korenke GC et al (1992) Proton NMR spectroscopy of cerebral metabolic alterations in infantile peroxisomal disorders. J Comput Assist Tomogr 16(3):335–344
4. Detre JA, Wang ZY, Bogdan AR et al (1991) Regional variation in brain lactate in Leigh syndrome by localized 1H magnetic resonance spectroscopy. Ann Neurol 29(2):218–221
5. Dreha-Kulaczewski SF, Dechent P, Finsterbusch J et al (2008) Early reduction of total N-acetyl-aspartate-compounds in patients with vanishing white matter disease. A long-term follow-up MRS study. Pediatr Res 63(4):444–449
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