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AJNR. American Journal of Neuroradiology
|
January 29, 2011
Correlating quantitative MR imaging with histopathology in X-linked adrenoleukodystrophy
J P van der Voorn, P J W Pouwels, J M Powers, et al.
Neuroscience
|
April 18, 2003
Expression and cellular distribution of multidrug transporter proteins in two major causes of medically intractable epilepsy: focal cortical dysplasia and glioneuronal tumors
E Aronica, J A Gorter, G H Jansen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 1, 1997
Autosomal dominant cerebellar ataxia with retinal degeneration (ADCA II): clinical and neuropathological findings in two pedigrees and genetic linkage to 3p12-p21.1
G J Jöbsis, J W Weber, P G Barth, et al.
Epilepsy Research
|
July 13, 2004
Alternative splicing of glutamate transporter EAAT2 RNA in neocortex and hippocampus of temporal lobe epilepsy patients
G Hoogland, R J van Oort, E A Proper, et al.
Neuroscience
|
December 21, 2007
Gene expression profile analysis of epilepsy-associated gangliogliomas
E Aronica, K Boer, A Becker, et al.
Neuropediatrics
|
June 10, 2005
Neonatal lactic acidosis, complex I/IV deficiency, and fetal cerebral disruption
H L M van Straaten, J P van Tintelen, J M F Trijbels, et al.
Neurobiology of Disease
|
April 7, 2007
Complement activation in experimental and human temporal lobe epilepsy
E Aronica, K Boer, E A van Vliet, et al.
Neuroscience
|
March 12, 2010
Tissue plasminogen activator and urokinase plasminogen activator in human epileptogenic pathologies
A M Iyer, E Zurolo, K Boer, et al.
Brain Pathology (Zurich, Switzerland)
|
October 30, 2016
ALS-Associated Endoplasmic Reticulum Proteins in Denervated Skeletal Muscle: Implications for Motor Neuron Disease Pathology
C M Jesse, E Bushuven, P Tripathi, et al.
Clinical Genetics
|
January 26, 2011
Childhood brain tumours due to germline bi-allelic mismatch repair gene mutations
P C Johannesma, H M van der Klift, N C T van Grieken, et al.
Page
of 15
Search research articles
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Showing results (131-140 of 141) with videos related to
Sort By:
Page
of 15
AJNR. American Journal of Neuroradiology
|
January 29, 2011
Correlating quantitative MR imaging with histopathology in X-linked adrenoleukodystrophy
J P van der Voorn, P J W Pouwels, J M Powers, et al.
Neuroscience
|
April 18, 2003
Expression and cellular distribution of multidrug transporter proteins in two major causes of medically intractable epilepsy: focal cortical dysplasia and glioneuronal tumors
E Aronica, J A Gorter, G H Jansen, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
April 1, 1997
Autosomal dominant cerebellar ataxia with retinal degeneration (ADCA II): clinical and neuropathological findings in two pedigrees and genetic linkage to 3p12-p21.1
G J Jöbsis, J W Weber, P G Barth, et al.
Epilepsy Research
|
July 13, 2004
Alternative splicing of glutamate transporter EAAT2 RNA in neocortex and hippocampus of temporal lobe epilepsy patients
G Hoogland, R J van Oort, E A Proper, et al.
Neuroscience
|
December 21, 2007
Gene expression profile analysis of epilepsy-associated gangliogliomas
E Aronica, K Boer, A Becker, et al.
Neuropediatrics
|
June 10, 2005
Neonatal lactic acidosis, complex I/IV deficiency, and fetal cerebral disruption
H L M van Straaten, J P van Tintelen, J M F Trijbels, et al.
Neurobiology of Disease
|
April 7, 2007
Complement activation in experimental and human temporal lobe epilepsy
E Aronica, K Boer, E A van Vliet, et al.
Neuroscience
|
March 12, 2010
Tissue plasminogen activator and urokinase plasminogen activator in human epileptogenic pathologies
A M Iyer, E Zurolo, K Boer, et al.
Brain Pathology (Zurich, Switzerland)
|
October 30, 2016
ALS-Associated Endoplasmic Reticulum Proteins in Denervated Skeletal Muscle: Implications for Motor Neuron Disease Pathology
C M Jesse, E Bushuven, P Tripathi, et al.
Clinical Genetics
|
January 26, 2011
Childhood brain tumours due to germline bi-allelic mismatch repair gene mutations
P C Johannesma, H M van der Klift, N C T van Grieken, et al.
Page
of 15