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J C Jen

Showing results (11-20 of 21) with videos related to

Pageof 3
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Neurology|September 28, 2005
Novel CCM1 mutation in a patient with paraparesis and thoracic cord cavernous malformationM F Waters, D C Shields, N A Martin, et al.
Neurology|June 30, 2005
CACNA1A mutations causing episodic and progressive ataxia alter channel trafficking and kineticsJ Wan, R Khanna, M Sandusky, et al.
Archives of Neurology|October 21, 1998
Oculomotor phenotypes in autosomal dominant ataxiasN Buttner, D Geschwind, J C Jen, et al.
American Journal of Medical Genetics|May 9, 2001
Familial benign recurrent vertigoA K Oh, H Lee, J C Jen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 25, 2007
Episodic vertical oscillopsia with progressive gait ataxia: clinical description of a new episodic syndrome and evidence of linkage to chromosome 13qY H Cha, H Lee, J C Jen, et al.
Brain : a Journal of Neurology|June 19, 2007
Primary episodic ataxias: diagnosis, pathogenesis and treatmentJ C Jen, T D Graves, E J Hess, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 17, 2007
Prolonged hemiplegic episodes in children due to mutations in ATP1A2J C Jen, A Klein, E Boltshauser, et al.
Neurology|December 30, 2004
Suggestive linkage to chromosome 6q in families with bilateral vestibulopathyJ C Jen, H Wang, H Lee, et al.
Neurology|July 8, 2011
A randomized trial of 4-aminopyridine in EA2 and related familial episodic ataxiasM Strupp, R Kalla, J Claassen, et al.
Neurology|August 9, 2006
Diffusion tensor MRI shows abnormal brainstem crossing fibers associated with ROBO3 mutationsN L Sicotte, G Salamon, D W Shattuck, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Neurology|September 28, 2005
Novel CCM1 mutation in a patient with paraparesis and thoracic cord cavernous malformationM F Waters, D C Shields, N A Martin, et al.
Neurology|June 30, 2005
CACNA1A mutations causing episodic and progressive ataxia alter channel trafficking and kineticsJ Wan, R Khanna, M Sandusky, et al.
Archives of Neurology|October 21, 1998
Oculomotor phenotypes in autosomal dominant ataxiasN Buttner, D Geschwind, J C Jen, et al.
American Journal of Medical Genetics|May 9, 2001
Familial benign recurrent vertigoA K Oh, H Lee, J C Jen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 25, 2007
Episodic vertical oscillopsia with progressive gait ataxia: clinical description of a new episodic syndrome and evidence of linkage to chromosome 13qY H Cha, H Lee, J C Jen, et al.
Brain : a Journal of Neurology|June 19, 2007
Primary episodic ataxias: diagnosis, pathogenesis and treatmentJ C Jen, T D Graves, E J Hess, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 17, 2007
Prolonged hemiplegic episodes in children due to mutations in ATP1A2J C Jen, A Klein, E Boltshauser, et al.
Neurology|December 30, 2004
Suggestive linkage to chromosome 6q in families with bilateral vestibulopathyJ C Jen, H Wang, H Lee, et al.
Neurology|July 8, 2011
A randomized trial of 4-aminopyridine in EA2 and related familial episodic ataxiasM Strupp, R Kalla, J Claassen, et al.
Neurology|August 9, 2006
Diffusion tensor MRI shows abnormal brainstem crossing fibers associated with ROBO3 mutationsN L Sicotte, G Salamon, D W Shattuck, et al.
Pageof 3