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S R Hammans

Showing results (1-10 of 31) with videos related to

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Essays in Biochemistry|January 1, 1994
Mitochondrial DNA and diseaseS R Hammans
Journal of Neurology, Neurosurgery, and Psychiatry|October 1, 1996
The inherited ataxias and the new geneticsS R Hammans
Journal of Neurology, Neurosurgery, and Psychiatry|February 1, 1989
Superior sagittal sinus thrombosis in Wegener's granulomatosisS R Hammans, L Ginsberg
British Journal of Hospital Medicine|July 1, 1991
Mitochondrial disease and mitochondrial DNAS R Hammans, A E Harding
Journal of Neurology, Neurosurgery, and Psychiatry|April 4, 1998
Ataxia with isolated vitamin E deficiency presenting as mutation negative Friedreich's ataxiaS R Hammans, C R Kennedy
Journal of Inherited Metabolic Disease|January 1, 1992
Deletions of the mitochondrial genomeA E Harding, S R Hammans
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1988
Chronic relapsing inflammatory polyneuropathy complicating sicca syndromeD Barnes, S R Hammans, N J Legg
European Journal of Neurology|April 4, 2001
Palatal palsy in dermatomyositisC J Price, J P Frankel, S R Hammans
Journal of Neurology|March 1, 1994
Cortical reflex myoclonus in patients with the mitochondrial DNA transfer RNA(Lys)(8344) (MERRF) mutationP D Thompson, S R Hammans, A E Harding
Journal of Neurology, Neurosurgery, and Psychiatry|April 18, 2003
Allgrove or 4 "A" syndrome: an autosomal recessive syndrome causing multisystem neurological diseaseJ Kimber, B N McLean, M Prevett, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
Essays in Biochemistry|January 1, 1994
Mitochondrial DNA and diseaseS R Hammans
Journal of Neurology, Neurosurgery, and Psychiatry|October 1, 1996
The inherited ataxias and the new geneticsS R Hammans
Journal of Neurology, Neurosurgery, and Psychiatry|February 1, 1989
Superior sagittal sinus thrombosis in Wegener's granulomatosisS R Hammans, L Ginsberg
British Journal of Hospital Medicine|July 1, 1991
Mitochondrial disease and mitochondrial DNAS R Hammans, A E Harding
Journal of Neurology, Neurosurgery, and Psychiatry|April 4, 1998
Ataxia with isolated vitamin E deficiency presenting as mutation negative Friedreich's ataxiaS R Hammans, C R Kennedy
Journal of Inherited Metabolic Disease|January 1, 1992
Deletions of the mitochondrial genomeA E Harding, S R Hammans
Journal of Neurology, Neurosurgery, and Psychiatry|January 1, 1988
Chronic relapsing inflammatory polyneuropathy complicating sicca syndromeD Barnes, S R Hammans, N J Legg
European Journal of Neurology|April 4, 2001
Palatal palsy in dermatomyositisC J Price, J P Frankel, S R Hammans
Journal of Neurology|March 1, 1994
Cortical reflex myoclonus in patients with the mitochondrial DNA transfer RNA(Lys)(8344) (MERRF) mutationP D Thompson, S R Hammans, A E Harding
Journal of Neurology, Neurosurgery, and Psychiatry|April 18, 2003
Allgrove or 4 "A" syndrome: an autosomal recessive syndrome causing multisystem neurological diseaseJ Kimber, B N McLean, M Prevett, et al.
Pageof 4