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R W Baloh

Showing results (221-230 of 257) with videos related to

Pageof 26
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Archives of Neurology|October 21, 1998
Oculomotor phenotypes in autosomal dominant ataxiasN Buttner, D Geschwind, J C Jen, et al.
The Laryngoscope|November 1, 1996
Histopathology of idiopathic chronic recurrent vertigoA Ishiyama, G P Ishiyama, I Lopez, et al.
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.
Journal of the American Geriatrics Society|April 1, 1994
Comparison of static and dynamic posturography in young and older normal peopleR W Baloh, T D Fife, L Zwerling, et al.
Investigative Ophthalmology & Visual Science|July 1, 1985
Velocities of vertical saccades with different eye movement recording methodsR D Yee, V L Schiller, V Lim, et al.
Neurology|July 17, 1999
A novel nonsense mutation in CACNA1A causes episodic ataxia and hemiplegiaJ Jen, Q Yue, S F Nelson, et al.
Neurology|December 31, 1997
Spinocerebellar ataxia type 6. Frequency of the mutation and genotype-phenotype correlationsD H Geschwind, S Perlman, K P Figueroa, et al.
American Journal of Medical Genetics|May 9, 2001
Familial benign recurrent vertigoA K Oh, H Lee, J C Jen, et al.
The Annals of Otology, Rhinology, and Laryngology|September 1, 1982
Comparison of vestibular subjective sensation and nystagmus responses during computerized harmonic acceleration testsV Honrubia, H A Jenkins, R W Baloh, et al.
Pageof 26

Showing results (221-230 of 257) with videos related to

Sort By:
Pageof 26
Archives of Neurology|October 21, 1998
Oculomotor phenotypes in autosomal dominant ataxiasN Buttner, D Geschwind, J C Jen, et al.
The Laryngoscope|November 1, 1996
Histopathology of idiopathic chronic recurrent vertigoA Ishiyama, G P Ishiyama, I Lopez, et al.
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.
Journal of the American Geriatrics Society|April 1, 1994
Comparison of static and dynamic posturography in young and older normal peopleR W Baloh, T D Fife, L Zwerling, et al.
Investigative Ophthalmology & Visual Science|July 1, 1985
Velocities of vertical saccades with different eye movement recording methodsR D Yee, V L Schiller, V Lim, et al.
Neurology|July 17, 1999
A novel nonsense mutation in CACNA1A causes episodic ataxia and hemiplegiaJ Jen, Q Yue, S F Nelson, et al.
Neurology|December 31, 1997
Spinocerebellar ataxia type 6. Frequency of the mutation and genotype-phenotype correlationsD H Geschwind, S Perlman, K P Figueroa, et al.
American Journal of Medical Genetics|May 9, 2001
Familial benign recurrent vertigoA K Oh, H Lee, J C Jen, et al.
The Annals of Otology, Rhinology, and Laryngology|September 1, 1982
Comparison of vestibular subjective sensation and nystagmus responses during computerized harmonic acceleration testsV Honrubia, H A Jenkins, R W Baloh, et al.
Pageof 26