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Showing results (1261-1270 of 1,434) with videos related to
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Hepatology (Baltimore, Md.)
|
January 22, 2011
Quantitation of pretreatment serum interferon-γ-inducible protein-10 improves the predictive value of an IL28B gene polymorphism for hepatitis C treatment response
Jama M Darling, Jeroen Aerssens, Gregory Fanning, et al.
Hepatology (Baltimore, Md.)
|
January 29, 2011
Inosine triphosphatase genetic variants are protective against anemia during antiviral therapy for HCV2/3 but do not decrease dose reductions of RBV or increase SVR
Alexander J Thompson, Rosanna Santoro, Valeria Piazzolla, et al.
Circulation
|
March 15, 2006
Guidelines for prevention of stroke in patients with ischemic stroke or transient ischemic attack: a statement for healthcare professionals from the American Heart Association/American Stroke Association Council on Stroke: co-sponsored by the Council on Cardiovascular Radiology and Intervention: the American Academy of Neurology affirms the value of this guideline
Ralph L Sacco, Robert Adams, Greg Albers, et al.
Kidney International
|
June 9, 2000
Comparative hospitalization of hemodialysis and peritoneal dialysis patients in Canada
S W Murphy, R N Foley, B J Barrett, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
December 25, 2018
Statin Safety and Associated Adverse Events: A Scientific Statement From the American Heart Association
Connie B Newman, David Preiss, Jonathan A Tobert, et al.
Epilepsy Research
|
November 4, 2008
No major role of common SV2A variation for predisposition or levetiracetam response in epilepsy
J M Lynch, S K Tate, P Kinirons, et al.
JAMA Network Open
|
April 5, 2023
Major Cardiovascular Events After Spontaneous Intracerebral Hemorrhage by Hematoma Location
Nils Jensen Boe, Stine Munk Hald, Mie Micheelsen Jensen, et al.
Frontiers in Cellular Neuroscience
|
June 5, 2023
Epilepsy in a mouse model of GNB1 encephalopathy arises from altered potassium (GIRK) channel signaling and is alleviated by a GIRK inhibitor
Sophie Colombo, Haritha P Reddy, Sabrina Petri, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
November 7, 2015
TECPR2 mutations cause a new subtype of familial dysautonomia like hereditary sensory autonomic neuropathy with intellectual disability
Gali Heimer, Danit Oz-Levi, Eran Eyal, et al.
Plos Computational Biology
|
October 2, 2018
meaRtools: An R package for the analysis of neuronal networks recorded on microelectrode arrays
Sahar Gelfman, Quanli Wang, Yi-Fan Lu, et al.
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of 144
Search research articles
Search
Showing results (1261-1270 of 1,434) with videos related to
Sort By:
Page
of 144
Hepatology (Baltimore, Md.)
|
January 22, 2011
Quantitation of pretreatment serum interferon-γ-inducible protein-10 improves the predictive value of an IL28B gene polymorphism for hepatitis C treatment response
Jama M Darling, Jeroen Aerssens, Gregory Fanning, et al.
Hepatology (Baltimore, Md.)
|
January 29, 2011
Inosine triphosphatase genetic variants are protective against anemia during antiviral therapy for HCV2/3 but do not decrease dose reductions of RBV or increase SVR
Alexander J Thompson, Rosanna Santoro, Valeria Piazzolla, et al.
Circulation
|
March 15, 2006
Guidelines for prevention of stroke in patients with ischemic stroke or transient ischemic attack: a statement for healthcare professionals from the American Heart Association/American Stroke Association Council on Stroke: co-sponsored by the Council on Cardiovascular Radiology and Intervention: the American Academy of Neurology affirms the value of this guideline
Ralph L Sacco, Robert Adams, Greg Albers, et al.
Kidney International
|
June 9, 2000
Comparative hospitalization of hemodialysis and peritoneal dialysis patients in Canada
S W Murphy, R N Foley, B J Barrett, et al.
Arteriosclerosis, Thrombosis, and Vascular Biology
|
December 25, 2018
Statin Safety and Associated Adverse Events: A Scientific Statement From the American Heart Association
Connie B Newman, David Preiss, Jonathan A Tobert, et al.
Epilepsy Research
|
November 4, 2008
No major role of common SV2A variation for predisposition or levetiracetam response in epilepsy
J M Lynch, S K Tate, P Kinirons, et al.
JAMA Network Open
|
April 5, 2023
Major Cardiovascular Events After Spontaneous Intracerebral Hemorrhage by Hematoma Location
Nils Jensen Boe, Stine Munk Hald, Mie Micheelsen Jensen, et al.
Frontiers in Cellular Neuroscience
|
June 5, 2023
Epilepsy in a mouse model of GNB1 encephalopathy arises from altered potassium (GIRK) channel signaling and is alleviated by a GIRK inhibitor
Sophie Colombo, Haritha P Reddy, Sabrina Petri, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
November 7, 2015
TECPR2 mutations cause a new subtype of familial dysautonomia like hereditary sensory autonomic neuropathy with intellectual disability
Gali Heimer, Danit Oz-Levi, Eran Eyal, et al.
Plos Computational Biology
|
October 2, 2018
meaRtools: An R package for the analysis of neuronal networks recorded on microelectrode arrays
Sahar Gelfman, Quanli Wang, Yi-Fan Lu, et al.
Page
of 144