Search research articles
Contact Us
Filters
Showing results (231-240 of 257) with videos related to
Page
of 26
Sort By:
Neurology
|
December 25, 2003
Presynaptic failure of neuromuscular transmission and synaptic remodeling in EA2
R A Maselli, J Wan, V Dunne, et al.
Investigative Ophthalmology & Visual Science
|
February 1, 1987
Eye movements in schizophrenia
R D Yee, R W Baloh, S R Marder, 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 13q
Y H Cha, H Lee, J C Jen, et al.
Lancet (London, England)
|
March 29, 1975
Neuropsychological dysfunction in children with chronic low-level lead absorption
P J Landrigan, R H Whitworth, R W Baloh, et al.
Neurology
|
December 31, 1997
Hereditary endotheliopathy with retinopathy, nephropathy, and stroke (HERNS)
J Jen, A H Cohen, Q Yue, et al.
Brain : a Journal of Neurology
|
June 19, 2007
Primary episodic ataxias: diagnosis, pathogenesis and treatment
J C Jen, T D Graves, E J Hess, et al.
Neurology
|
February 16, 2006
Pontine and cerebellar atrophy correlate with clinical disability in SCA2
S H Ying, S I Choi, S L Perlman, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 17, 2007
Prolonged hemiplegic episodes in children due to mutations in ATP1A2
J C Jen, A Klein, E Boltshauser, et al.
Neurology
|
May 29, 2003
Nodulus infarction mimicking acute peripheral vestibulopathy
H Lee, H A Yi, Y W Cho, et al.
Neurology
|
August 15, 2002
Familial horizontal gaze palsy with progressive scoliosis maps to chromosome 11q23-25
Joanna Jen, C J Coulin, T M Bosley, et al.
Page
of 26
Search research articles
Search
Showing results (231-240 of 257) with videos related to
Sort By:
Page
of 26
Neurology
|
December 25, 2003
Presynaptic failure of neuromuscular transmission and synaptic remodeling in EA2
R A Maselli, J Wan, V Dunne, et al.
Investigative Ophthalmology & Visual Science
|
February 1, 1987
Eye movements in schizophrenia
R D Yee, R W Baloh, S R Marder, 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 13q
Y H Cha, H Lee, J C Jen, et al.
Lancet (London, England)
|
March 29, 1975
Neuropsychological dysfunction in children with chronic low-level lead absorption
P J Landrigan, R H Whitworth, R W Baloh, et al.
Neurology
|
December 31, 1997
Hereditary endotheliopathy with retinopathy, nephropathy, and stroke (HERNS)
J Jen, A H Cohen, Q Yue, et al.
Brain : a Journal of Neurology
|
June 19, 2007
Primary episodic ataxias: diagnosis, pathogenesis and treatment
J C Jen, T D Graves, E J Hess, et al.
Neurology
|
February 16, 2006
Pontine and cerebellar atrophy correlate with clinical disability in SCA2
S H Ying, S I Choi, S L Perlman, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 17, 2007
Prolonged hemiplegic episodes in children due to mutations in ATP1A2
J C Jen, A Klein, E Boltshauser, et al.
Neurology
|
May 29, 2003
Nodulus infarction mimicking acute peripheral vestibulopathy
H Lee, H A Yi, Y W Cho, et al.
Neurology
|
August 15, 2002
Familial horizontal gaze palsy with progressive scoliosis maps to chromosome 11q23-25
Joanna Jen, C J Coulin, T M Bosley, et al.
Page
of 26