Isolated pyramidal tract impairment in the central nervous system of adult-onset Krabbe disease with novel mutations in the GALC gene

[1]  R. Hanajima,et al.  Cortico-conus motor conduction time (CCCT) for leg muscles , 2010, Clinical Neurophysiology.

[2]  T. Matsukawa,et al.  Efferent and afferent evoked potentials in patients with adrenomyeloneuropathy , 2010, Clinical Neurology and Neurosurgery.

[3]  R. Raininko,et al.  The earliest MR imaging and proton MR spectroscopy abnormalities in adult‐onset Krabbe disease , 2007, Acta neurologica Scandinavica.

[4]  M. Taniike,et al.  Six novel mutations detected in the GALC gene in 17 Japanese patients with Krabbe disease, and new genotype-phenotype correlation , 2006, Journal of Human Genetics.

[5]  R. Henderson,et al.  Adult onset Krabbe disease may mimic motor neurone disease , 2003, Journal of Clinical Neuroscience.

[6]  Kunihiko Suzuki.  Globoid Cell Leukodystrophy (Krabbe's Disease): Update , 2003, Journal of child neurology.

[7]  N. De Stefano,et al.  Evidence of diffuse brain pathology and unspecific genetic characterization in a patient with an atypical form of adult-onset Krabbe disease , 2000, Journal of Neurology.

[8]  Y. Okada,et al.  Measurements of magnetic signals from the subcortical trigeminal somatosensory system in juvenile swine , 1995 .

[9]  H. Fukuyama,et al.  Electrophysiological studies of adult-type Krabbe's disease , 1995 .

[10]  R. Hanajima,et al.  Magnetic stimulation of corticospinal pathways at the foramen magnum level in humans , 1994, Annals of neurology.

[11]  K. Hasuo,et al.  Late Infantile Krabbe Leukodystrophy: MRI and Evoked Potentials in a Japanese Girl , 1987, Neuropediatrics.