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Mitochondrial DNA deletion in an 8-year-old boy with Pearson syndrome.
Baerlocher KE, Feldges A, Weissert M, Simonsz HJ, Rötig A. Baerlocher KE, et al. Among authors: weissert m. J Inherit Metab Dis. 1992;15(3):327-30. doi: 10.1007/BF02435968. J Inherit Metab Dis. 1992. PMID: 1405465 Free article. No abstract available.
Outcome of severe unilateral cerebellar hypoplasia.
Poretti A, Limperopoulos C, Roulet-Perez E, Wolf NI, Rauscher C, Prayer D, Müller A, Weissert M, Kotzaeridou U, Du Plessis AJ, Huisman TA, Boltshauser E. Poretti A, et al. Among authors: weissert m. Dev Med Child Neurol. 2010 Aug;52(8):718-24. doi: 10.1111/j.1469-8749.2009.03522.x. Epub 2009 Oct 23. Dev Med Child Neurol. 2010. PMID: 19863638 Free article.
Vanishing cerebellum in myelomeningocoele.
Boltshauser E, Schneider J, Kollias S, Waibel P, Weissert M. Boltshauser E, et al. Among authors: weissert m. Eur J Paediatr Neurol. 2002;6(2):109-13. doi: 10.1053/ejpn.2001.0556. Eur J Paediatr Neurol. 2002. PMID: 11995957
26 results