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Klinische Padiatrie|September 23, 1998
Monitoring tumor activity in low grade glioma of childhoodG Mölenkamp, B Riemann, T Kuwert, et al.Fortschritte Der Neurologie-Psychiatrie|April 8, 1998
[Hereditary neural amyotrophy (HNA): clinical and molecular genetic basis]F Stögbauer, P Young, G Kuhlenbäumer, et al.Neurosurgical Review|May 19, 1998
High amino acid uptake in a low-grade desmoplastic infantile ganglioglioma in a 14-year-old patientB Woesler, T Kuwert, G Kurlemann, et al.Human Genetics|December 1, 1991
A specific point mutation in the mitochondrial genome of Caucasians with MELASC Enter, J Müller-Höcker, S Zierz, et al.Nuklearmedizin. Nuclear Medicine|September 16, 2005
[Clinical value of amino acid imaging in paediatric brain tumours. Comparison with MRI]K Lang, S Kloska, R Straeter, et al.European Journal of Nuclear Medicine|April 24, 2001
High uptake of L-3-[123I]iodo-alpha-methyl tyrosine in pilocytic astrocytomasM Weckesser, P Matheja, C H Rickert, et al.American Journal of Medical Genetics|September 5, 1997
Leukodystrophy incidence in GermanyP Heim, M Claussen, B Hoffmann, et al.European Journal of Neurology|October 6, 2007
Isoform-specific increase of spastin stability by N-terminal missense variants including intragenic modifiers of SPG4 hereditary spastic paraplegiaJ Schickel, T Pamminger, A Ehrsam, et al.Human Mutation|March 26, 2003
Identification of seven novel mutations in the GAN geneP Bomont, C Ioos, C Yalcinkaya, et al.Klinische Padiatrie|July 21, 2005
[Optimizing epilepsy therapy in children and adolescents with lamotrigine]H Siemes, U Brandl, C Helmstädter, et al.Pageof 9