Showing results (91-100 of 7,579) with videos related to
Sort By:
Pageof 758
Acta Neuropathologica|November 28, 1977
Generalized giant axonal neuropathy: a filament-forming disease of neuronal, endothelial, glial, and schwann cells in a patient without kinky hairJ Peiffer, W Schlote, A Bischoff, et al.Neuropediatrics|February 1, 1985
Heterogeneity of congenital motor and sensory neuropathiesJ Lütschg, F Vassella, E Boltshauser, et al.Human Genetics|December 1, 1988
Pelizaeus-Merzbacher disease: identification of heterozygotes with magnetic resonance imaging?E Boltshauser, A Schinzel, W Wichmann, et al.European Journal of Pediatrics|August 1, 1988
Short stature: a common feature in Duchenne muscular dystrophyU Eiholzer, E Boltshauser, D Frey, et al.Neurology|September 26, 1997
Diagnostic value of cerebrospinal fluid examination in children with peripheral facial palsy and suspected Lyme borreliosisM Albisetti, G Schaer, M Good, et al.Neuropediatrics|September 10, 1999
Visual field constriction is not limited to children treated with vigabatrinG Wohlrab, E Boltshauser, B Schmitt, et al.European Journal of Pediatrics|December 11, 1999
Neonatal Escherichia coli meningitis: spinal adhesions as a late complicationM Steinlin, B Knecht, D Könü, et al.Journal of Neuroradiology = Journal De Neuroradiologie|January 23, 2009
Fetal magnetic resonance imaging in midline malformations of the central nervous system and review of the literatureP Dill, A Poretti, E Boltshauser, et al.Prenatal Diagnosis|February 1, 1989
Prenatal diagnosis of Schwartz-Jampel syndrome with early manifestationU A Hunziker, G Savoldelli, E Boltshauser, et al.Neuropediatrics|September 13, 2006
Acute flaccid paralysis as initial symptom in 4 patients with novel E1alpha mutations of the pyruvate dehydrogenase complexH M Strassburg, J Koch, J Mayr, et al.Pageof 758