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Annals of Neurology
|
February 24, 2001
Variable phenotype of Alzheimer's disease with spastic paraparesis
M J Smith, J B Kwok, C A McLean, et al.
Nanomedicine : Nanotechnology, Biology, and Medicine
|
May 24, 2011
Sizing and phenotyping of cellular vesicles using Nanoparticle Tracking Analysis
Rebecca A Dragovic, Christopher Gardiner, Alexandra S Brooks, et al.
Neuroscience Letters
|
October 29, 1998
No association of presenilin-1 intronic polymorphism and Alzheimer's disease in Australia
K Taddei, D Yang, C Fisher, et al.
European Journal of Human Genetics : EJHG
|
January 9, 2014
Structural and numerical changes of chromosome X in patients with esophageal atresia
Erwin Brosens, Elisabeth M de Jong, Tahsin Stefan Barakat, et al.
BMC Neurology
|
August 30, 2008
Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9
Agnes A Luty, John B J Kwok, Elizabeth M Thompson, et al.
Physical Review Letters
|
March 5, 2009
Chemical pressure induced spin freezing phase transition in kagome pr langasites
H D Zhou, C R Wiebe, Y-J Jo, et al.
Neurology
|
June 20, 2020
Longitudinal changes of brain microstructure and function in nonconcussed female rugby players
Kathryn Y Manning, Jeffrey S Brooks, James P Dickey, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology
|
May 13, 2015
Neuropathologic assessment of participants in two multi-center longitudinal observational studies: the Alzheimer Disease Neuroimaging Initiative (ADNI) and the Dominantly Inherited Alzheimer Network (DIAN)
Nigel J Cairns, Richard J Perrin, Erin E Franklin, et al.
European Journal of Human Genetics : EJHG
|
January 10, 2019
Biallelic sequence variants in INTS1 in patients with developmental delays, cataracts, and craniofacial anomalies
Max Krall, Stephanie Htun, Rhonda E Schnur, et al.
The Journal of Biological Chemistry
|
December 21, 2002
Presenilin-1 mutation L271V results in altered exon 8 splicing and Alzheimer's disease with non-cored plaques and no neuritic dystrophy
John B J Kwok, Glenda M Halliday, William S Brooks, et al.
Page
of 73
Search research articles
Search
Showing results (591-600 of 728) with videos related to
Sort By:
Page
of 73
Annals of Neurology
|
February 24, 2001
Variable phenotype of Alzheimer's disease with spastic paraparesis
M J Smith, J B Kwok, C A McLean, et al.
Nanomedicine : Nanotechnology, Biology, and Medicine
|
May 24, 2011
Sizing and phenotyping of cellular vesicles using Nanoparticle Tracking Analysis
Rebecca A Dragovic, Christopher Gardiner, Alexandra S Brooks, et al.
Neuroscience Letters
|
October 29, 1998
No association of presenilin-1 intronic polymorphism and Alzheimer's disease in Australia
K Taddei, D Yang, C Fisher, et al.
European Journal of Human Genetics : EJHG
|
January 9, 2014
Structural and numerical changes of chromosome X in patients with esophageal atresia
Erwin Brosens, Elisabeth M de Jong, Tahsin Stefan Barakat, et al.
BMC Neurology
|
August 30, 2008
Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9
Agnes A Luty, John B J Kwok, Elizabeth M Thompson, et al.
Physical Review Letters
|
March 5, 2009
Chemical pressure induced spin freezing phase transition in kagome pr langasites
H D Zhou, C R Wiebe, Y-J Jo, et al.
Neurology
|
June 20, 2020
Longitudinal changes of brain microstructure and function in nonconcussed female rugby players
Kathryn Y Manning, Jeffrey S Brooks, James P Dickey, et al.
Neuropathology : Official Journal of the Japanese Society of Neuropathology
|
May 13, 2015
Neuropathologic assessment of participants in two multi-center longitudinal observational studies: the Alzheimer Disease Neuroimaging Initiative (ADNI) and the Dominantly Inherited Alzheimer Network (DIAN)
Nigel J Cairns, Richard J Perrin, Erin E Franklin, et al.
European Journal of Human Genetics : EJHG
|
January 10, 2019
Biallelic sequence variants in INTS1 in patients with developmental delays, cataracts, and craniofacial anomalies
Max Krall, Stephanie Htun, Rhonda E Schnur, et al.
The Journal of Biological Chemistry
|
December 21, 2002
Presenilin-1 mutation L271V results in altered exon 8 splicing and Alzheimer's disease with non-cored plaques and no neuritic dystrophy
John B J Kwok, Glenda M Halliday, William S Brooks, et al.
Page
of 73