Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Eric T Quach"'
Autor:
Eric T. Quach, Amir R. Dehdashti
Publikováno v:
32nd Annual Meeting North American Skull Base Society.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9847572c6c1178494a343f01b3337d70
https://doi.org/10.1055/s-0043-1762524
https://doi.org/10.1055/s-0043-1762524
Autor:
Eric T. Quach, Amir R. Dehdashti
Publikováno v:
32nd Annual Meeting North American Skull Base Society.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::deb3f5f6a489407e6758366adae10c24
https://doi.org/10.1055/s-0043-1762529
https://doi.org/10.1055/s-0043-1762529
Autor:
Eric T. Quach, Amir R. Dehdashti
Publikováno v:
32nd Annual Meeting North American Skull Base Society.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2cb1ae4168581e04162b153a1225eae
https://doi.org/10.1055/s-0043-1762531
https://doi.org/10.1055/s-0043-1762531
Autor:
Eric T. Quach, Amir R. Dehdashti
Publikováno v:
32nd Annual Meeting North American Skull Base Society.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c33afab57c290c3f29c55fba0a3c41d8
https://doi.org/10.1055/s-0043-1762544
https://doi.org/10.1055/s-0043-1762544
Autor:
Eleanor M. Donnelly, Eric T. Quach, Terence M. Hillery, Brenten L. Heeke, Brooke R. Snyder, Chalonda R. Handy, Deirdre M. O'Connor, Nicholas M. Boulis, Thais Federici
Publikováno v:
Neurobiology of Disease, Vol 45, Iss 3, Pp 992-998 (2012)
Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disease, which is the leading genetic cause of mortality in children. To date no effective treatment exists for SMA. The genetic basis for SMA has been well documented as a mutatio
Externí odkaz:
https://doaj.org/article/8b865ceb2cc341f8b50a0739c7a8b385
Autor:
Eric T, Quach, Rami O, Almefty
Publikováno v:
Operative Neurosurgery. 22:e262-e263
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e2276777d6a96421b716f5eef7f59b53
https://doi.org/10.1227/ons.0000000000000203
https://doi.org/10.1227/ons.0000000000000203
A conditioning lesion provides selective protection in a rat model of Amyotrophic Lateral Sclerosis.
Autor:
Colin K Franz, Eric T Quach, Christina A Krudy, Thais Federici, Michele A Kliem, Brooke R Snyder, Bethwel Raore, Nicholas M Boulis
Publikováno v:
PLoS ONE, Vol 4, Iss 10, p e7357 (2009)
BACKGROUND:Amyotrophic Lateral Sclerosis (ALS) is neurodegenerative disease characterized by muscle weakness and atrophy due to progressive motoneuron loss. The death of motoneuron is preceded by the failure of neuromuscular junctions (NMJs) and axon
Externí odkaz:
https://doaj.org/article/90b32f7c00244afcb29f10012761057f
Publikováno v:
Journal of Clinical Neuroscience. 22:1515-1518
We present the first report, to our knowledge, in which revascularization of the middle cerebral artery (MCA) with a high flow extracranial-intracranial procedure resulted in symptomatic hyperemia of the posterior circulation. Cerebral hyperperfusion
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8630d5cede531344eca4ad4add3d00d3
https://doi.org/10.1016/j.jocn.2015.03.022
https://doi.org/10.1016/j.jocn.2015.03.022
Autor:
Eric T. Quach, Thais Federici, Nicholas M. Boulis, Chalonda R. Handy, Eleanor M. Donnelly, Brooke R. Snyder, Brenten L. Heeke, Deirdre M. O’Connor, Terence M. Hillery
Publikováno v:
Neurobiology of Disease, Vol 45, Iss 3, Pp 992-998 (2012)
Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disease, which is the leading genetic cause of mortality in children. To date no effective treatment exists for SMA. The genetic basis for SMA has been well documented as a mutatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ee5215143faed197d6e55950fa4c593
http://www.sciencedirect.com/science/article/pii/S0969996111003937
http://www.sciencedirect.com/science/article/pii/S0969996111003937
Comparison of adeno-associated viral vector serotypes for spinal cord and motor neuron gene delivery
Autor:
Thais Federici, Steven J. Gray, R. Jude Samulski, Jeremiah W. Huang, Cary H. Leung, Brooke R. Snyder, Eric T. Quach, Nicholas M. Boulis
Publikováno v:
Human gene therapy. 22(9)
Gene therapy for motor neuron diseases requires efficient gene delivery to motor neurons (MNs) throughout the spinal cord and brainstem. The present study compared adeno-associated viral (AAV) vector serotypes 1, 6, 8, and 9 for spinal cord delivery
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e00f64f1361707947738ccfcc6c66a33
https://pubmed.ncbi.nlm.nih.gov/21443428
https://pubmed.ncbi.nlm.nih.gov/21443428