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Brain Research
|
May 4, 2007
"Therapeutic time window" duration decreases with increasing severity of cerebral hypoxia-ischaemia under normothermia and delayed hypothermia in newborn piglets
Osuke Iwata, Sachiko Iwata, John S Thornton, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences
|
October 14, 2008
Central and peripheral pathology of kuru: pathological analysis of a recent case and comparison with other forms of human prion disease
Sebastian Brandner, Jerome Whitfield, Ken Boone, et al.
Annals of Neurology
|
September 1, 2005
Lewy body Parkinson's disease in a large pedigree with 77 Parkin mutation carriers
Peter P Pramstaller, Michael G Schlossmacher, Thomas S Jacques, et al.
Magnetic Resonance in Medicine
|
January 30, 2008
Quantitative magnetic resonance of postmortem multiple sclerosis brain before and after fixation
Klaus Schmierer, Claudia A M Wheeler-Kingshott, Daniel J Tozer, et al.
Annals of Neurology
|
February 26, 2005
Fewer thymic changes in MuSK antibody-positive than in MuSK antibody-negative MG
Maria Isabel Leite, Philipp Ströbel, Margaret Jones, et al.
The American Journal of Pathology
|
August 7, 2007
Myasthenia gravis thymus: complement vulnerability of epithelial and myoid cells, complement attack on them, and correlations with autoantibody status
Maria I Leite, Margaret Jones, Philipp Ströbel, et al.
Critical Care (London, England)
|
October 24, 2017
Translational evidence for two distinct patterns of neuroaxonal injury in sepsis: a longitudinal, prospective translational study
Johannes Ehler, Lucinda K Barrett, Valerie Taylor, et al.
Annals of Neurology
|
June 29, 2005
Depth of delayed cooling alters neuroprotection pattern after hypoxia-ischemia
Osuke Iwata, John S Thornton, Mark W Sellwood, et al.
Human Molecular Genetics
|
July 23, 2003
Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4 ) gene
Ming-Jen Lee, Dennis A Stephenson, Michael J Groves, et al.
Page
of 4
Search research articles
Search
Showing results (31-40 of 39) with videos related to
Sort By:
Page
of 4
You have reached the last page of results.
This site can display upto 39 results.
Brain Research
|
May 4, 2007
"Therapeutic time window" duration decreases with increasing severity of cerebral hypoxia-ischaemia under normothermia and delayed hypothermia in newborn piglets
Osuke Iwata, Sachiko Iwata, John S Thornton, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences
|
October 14, 2008
Central and peripheral pathology of kuru: pathological analysis of a recent case and comparison with other forms of human prion disease
Sebastian Brandner, Jerome Whitfield, Ken Boone, et al.
Annals of Neurology
|
September 1, 2005
Lewy body Parkinson's disease in a large pedigree with 77 Parkin mutation carriers
Peter P Pramstaller, Michael G Schlossmacher, Thomas S Jacques, et al.
Magnetic Resonance in Medicine
|
January 30, 2008
Quantitative magnetic resonance of postmortem multiple sclerosis brain before and after fixation
Klaus Schmierer, Claudia A M Wheeler-Kingshott, Daniel J Tozer, et al.
Annals of Neurology
|
February 26, 2005
Fewer thymic changes in MuSK antibody-positive than in MuSK antibody-negative MG
Maria Isabel Leite, Philipp Ströbel, Margaret Jones, et al.
The American Journal of Pathology
|
August 7, 2007
Myasthenia gravis thymus: complement vulnerability of epithelial and myoid cells, complement attack on them, and correlations with autoantibody status
Maria I Leite, Margaret Jones, Philipp Ströbel, et al.
Critical Care (London, England)
|
October 24, 2017
Translational evidence for two distinct patterns of neuroaxonal injury in sepsis: a longitudinal, prospective translational study
Johannes Ehler, Lucinda K Barrett, Valerie Taylor, et al.
Annals of Neurology
|
June 29, 2005
Depth of delayed cooling alters neuroprotection pattern after hypoxia-ischemia
Osuke Iwata, John S Thornton, Mark W Sellwood, et al.
Human Molecular Genetics
|
July 23, 2003
Hereditary sensory neuropathy is caused by a mutation in the delta subunit of the cytosolic chaperonin-containing t-complex peptide-1 (Cct4 ) gene
Ming-Jen Lee, Dennis A Stephenson, Michael J Groves, et al.
Page
of 4