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Archives of Neurology
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June 19, 2001
Cellular distribution of torsin A and torsin B in normal human brain
M Konakova, D P Huynh, W Yong, et al.
Human Genetics
|
January 1, 1996
Identification of three neurofibromatosis type 2 (NF2) gene mutations in vestibular schwannomas
J Sainz, K Figueroa, M E Baser, et al.
Human Genetics
|
April 1, 1995
A 163-bp deletion in the neurofibromatosis 2 (NF2) gene associated with variant phenotypes [corrected]
L Kluwe, S M Pulst, J Köppen, et al.
Nature Genetics
|
September 6, 2000
Nuclear localization or inclusion body formation of ataxin-2 are not necessary for SCA2 pathogenesis in mouse or human
D P Huynh, K Figueroa, N Hoang, et al.
Neurology
|
December 1, 1991
Familial spinal neurofibromatosis: clinical and DNA linkage analysis
S M Pulst, V M Riccardi, P Fain, et al.
Genomics
|
July 1, 1989
The Alzheimer amyloid precursor protein maps to human chromosome 21 bands q21.105-q21.05
J R Korenberg, S M Pulst, R L Neve, et al.
Cell Growth & Differentiation : the Molecular Biology Journal of the American Association for Cancer Research
|
November 1, 1996
Expression of neurofibromatosis 2 transcript and gene product during mouse fetal development
D P Huynh, T M Tran, T Nechiporuk, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
August 24, 1999
Electrical inexcitability of nerves and muscles in severe infantile spinal muscular atrophy
A A Kuo, S M Pulst, D S Eliashiv, et al.
Genomics
|
April 16, 1998
Genomic structure of the human gene for spinocerebellar ataxia type 2 (SCA2) on chromosome 12q24.1
S Sahba, A Nechiporuk, K P Figueroa, et al.
Neurosurgery
|
July 1, 1993
Neurofibromatosis 2 in the pediatric age group
V F Mautner, M Tatagiba, R Guthoff, et al.
Page
of 11
Search research articles
Search
Showing results (41-50 of 106) with videos related to
Sort By:
Page
of 11
Archives of Neurology
|
June 19, 2001
Cellular distribution of torsin A and torsin B in normal human brain
M Konakova, D P Huynh, W Yong, et al.
Human Genetics
|
January 1, 1996
Identification of three neurofibromatosis type 2 (NF2) gene mutations in vestibular schwannomas
J Sainz, K Figueroa, M E Baser, et al.
Human Genetics
|
April 1, 1995
A 163-bp deletion in the neurofibromatosis 2 (NF2) gene associated with variant phenotypes [corrected]
L Kluwe, S M Pulst, J Köppen, et al.
Nature Genetics
|
September 6, 2000
Nuclear localization or inclusion body formation of ataxin-2 are not necessary for SCA2 pathogenesis in mouse or human
D P Huynh, K Figueroa, N Hoang, et al.
Neurology
|
December 1, 1991
Familial spinal neurofibromatosis: clinical and DNA linkage analysis
S M Pulst, V M Riccardi, P Fain, et al.
Genomics
|
July 1, 1989
The Alzheimer amyloid precursor protein maps to human chromosome 21 bands q21.105-q21.05
J R Korenberg, S M Pulst, R L Neve, et al.
Cell Growth & Differentiation : the Molecular Biology Journal of the American Association for Cancer Research
|
November 1, 1996
Expression of neurofibromatosis 2 transcript and gene product during mouse fetal development
D P Huynh, T M Tran, T Nechiporuk, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
August 24, 1999
Electrical inexcitability of nerves and muscles in severe infantile spinal muscular atrophy
A A Kuo, S M Pulst, D S Eliashiv, et al.
Genomics
|
April 16, 1998
Genomic structure of the human gene for spinocerebellar ataxia type 2 (SCA2) on chromosome 12q24.1
S Sahba, A Nechiporuk, K P Figueroa, et al.
Neurosurgery
|
July 1, 1993
Neurofibromatosis 2 in the pediatric age group
V F Mautner, M Tatagiba, R Guthoff, et al.
Page
of 11