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Annals of the New York Academy of Sciences
|
December 10, 1999
Correlation between weakness and axonal loss in patients with CMT1A
K Krajewski, C Turansky, R Lewis, et al.
Acta Neuropathologica
|
January 28, 2004
Age-related axonal and myelin changes in the rumpshaker mutation of the Plp gene
J M Edgar, M McLaughlin, J A Barrie, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
September 1, 1997
Evidence that the homeodomain protein Gtx is involved in the regulation of oligodendrocyte myelination
R Awatramani, S Scherer, J Grinspan, et al.
Journal of Neuroscience Research
|
August 10, 2000
Gtx, an oligodendrocyte-specific homeodomain protein, has repressor activity
R Awatramani, J Beesley, H Yang, et al.
Neurology
|
January 21, 2009
X-linked distal hereditary motor neuropathy maps to the DSMAX locus on chromosome Xq13.1-q21
M Kennerson, G Nicholson, B Kowalski, et al.
Brain : a Journal of Neurology
|
June 27, 2000
Neurological dysfunction and axonal degeneration in Charcot-Marie-Tooth disease type 1A
K M Krajewski, R A Lewis, D R Fuerst, et al.
Brain : a Journal of Neurology
|
January 29, 2000
Charcot-Marie-Tooth disease type 1: molecular pathogenesis to gene therapy
J Kamholz, D Menichella, A Jani, et al.
AJNR. American Journal of Neuroradiology
|
November 26, 2011
Assessing abnormal iron content in the deep gray matter of patients with multiple sclerosis versus healthy controls
C A Habib, M Liu, N Bawany, et al.
Journal of Neurobiology
|
July 6, 2000
Proteolipid protein mRNA stability is regulated by axonal contact in the rodent peripheral nervous system
H Jiang, C S Duchala, R Awatramani, et al.
Journal of Lipid Research
|
May 16, 2001
Sterols in blood of normal and Smith-Lemli-Opitz subjects
B Ruan, W K Wilson, J Pang, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 20) with videos related to
Sort By:
Page
of 2
You have reached the last page of results.
This site can display upto 20 results.
Annals of the New York Academy of Sciences
|
December 10, 1999
Correlation between weakness and axonal loss in patients with CMT1A
K Krajewski, C Turansky, R Lewis, et al.
Acta Neuropathologica
|
January 28, 2004
Age-related axonal and myelin changes in the rumpshaker mutation of the Plp gene
J M Edgar, M McLaughlin, J A Barrie, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
September 1, 1997
Evidence that the homeodomain protein Gtx is involved in the regulation of oligodendrocyte myelination
R Awatramani, S Scherer, J Grinspan, et al.
Journal of Neuroscience Research
|
August 10, 2000
Gtx, an oligodendrocyte-specific homeodomain protein, has repressor activity
R Awatramani, J Beesley, H Yang, et al.
Neurology
|
January 21, 2009
X-linked distal hereditary motor neuropathy maps to the DSMAX locus on chromosome Xq13.1-q21
M Kennerson, G Nicholson, B Kowalski, et al.
Brain : a Journal of Neurology
|
June 27, 2000
Neurological dysfunction and axonal degeneration in Charcot-Marie-Tooth disease type 1A
K M Krajewski, R A Lewis, D R Fuerst, et al.
Brain : a Journal of Neurology
|
January 29, 2000
Charcot-Marie-Tooth disease type 1: molecular pathogenesis to gene therapy
J Kamholz, D Menichella, A Jani, et al.
AJNR. American Journal of Neuroradiology
|
November 26, 2011
Assessing abnormal iron content in the deep gray matter of patients with multiple sclerosis versus healthy controls
C A Habib, M Liu, N Bawany, et al.
Journal of Neurobiology
|
July 6, 2000
Proteolipid protein mRNA stability is regulated by axonal contact in the rodent peripheral nervous system
H Jiang, C S Duchala, R Awatramani, et al.
Journal of Lipid Research
|
May 16, 2001
Sterols in blood of normal and Smith-Lemli-Opitz subjects
B Ruan, W K Wilson, J Pang, et al.
Page
of 2