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Brain : a Journal of Neurology|June 1, 1995
From the syndrome of Charcot, Marie and Tooth to disorders of peripheral myelin proteinsA E HardingBailliere'S Clinical Neurology|November 1, 1995
Molecular genetics of peripheral neuropathiesA E HardingCurrent Opinion in Neurology and Neurosurgery|October 1, 1992
Molecular genetics and clinical aspects of inherited disorders of nerve and muscleA E HardingAdvances and Technical Standards in Neurosurgery|January 1, 1993
Clinical and molecular neurogenetics in neurosurgeryA E HardingJournal of the Neurological Sciences|August 1, 1981
"Idiopathic" late onset cerebellar ataxia. A clinical and genetic study of 36 casesA E HardingBrain : a Journal of Neurology|March 1, 1982
The clinical features and classification of the late onset autosomal dominant cerebellar ataxias. A study of 11 families, including descendants of the 'the Drew family of Walworth'A E HardingJournal of Neurology, Neurosurgery, and Psychiatry|August 1, 1984
Rupture of intracranial vascular lesions during arteriographyS A Tsementzis, R P Kennett, E R HitchcockJournal of Neurology, Neurosurgery, and Psychiatry|December 1, 1987
Susceptibility to pressure neuropathy distal to a constricting ligature in the guinea-pigT Shimpo, R W Gilliatt, R P Kennett, et al.Journal of Neurology, Neurosurgery, and Psychiatry|February 1, 1994
Changes in focal interictal epileptiform activity during and after the performance of verbal and visuospatial tasks in a patient with intractable partial seizuresS J Boniface, R P Kennett, J M Oxbury, et al.Pageof 21