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Magnetic Resonance in Medicine
|
July 27, 2007
T(1) relaxation in in vivo mouse brain at ultra-high field
Rob C G van de Ven, Bianca Hogers, Arn M J M van den Maagdenberg, et al.
Journal of Lipid Research
|
December 22, 2016
Quantitative profiling of endocannabinoids and related <i>N</i>-acylethanolamines in human CSF using nano LC-MS/MS
Vasudev Kantae, Shinji Ogino, Marek Noga, et al.
The Journal of Clinical Investigation
|
April 3, 2012
Hepatocyte-specific mutation of both NF-κB RelA and STAT3 abrogates the acute phase response in mice
Lee J Quinton, Matthew T Blahna, Matthew R Jones, et al.
Strahlentherapie Und Onkologie : Organ Der Deutschen Rontgengesellschaft ... [Et Al]
|
December 24, 2011
Prospective phase II trial of cetuximab plus VMAT-SIB in locally advanced head and neck squamous cell carcinoma. Feasibility and tolerability in elderly and chemotherapy-ineligible patients
F Alongi, M Bignardi, I Garassino, et al.
Archives of Neurology
|
May 21, 2003
Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraine
E E Kors, J Haan, N J Giffin, et al.
Neurology
|
August 5, 2018
RVCL-S and CADASIL display distinct impaired vascular function
Irene de Boer, Anine H Stam, Linde Buntinx, et al.
Journal of the American Society for Mass Spectrometry
|
April 17, 2015
Large-scale mass spectrometry imaging investigation of consequences of cortical spreading depression in a transgenic mouse model of migraine
Ricardo J Carreira, Reinald Shyti, Benjamin Balluff, et al.
Neuropediatrics
|
November 10, 2004
Alternating hemiplegia of childhood: no mutations in the second familial hemiplegic migraine gene ATP1A2
E E Kors, K R J Vanmolkot, J Haan, et al.
Cephalalgia : an International Journal of Headache
|
November 25, 2005
The 3p21.1-p21.3 hereditary vascular retinopathy locus increases the risk for Raynaud's phenomenon and migraine
J J Hottenga, K R J Vanmolkot, E E Kors, et al.
Annals of Neurology
|
December 21, 2005
Migraine and MTHFR C677T genotype in a population-based sample
Ann I Scher, Gisela M Terwindt, W M Monique Verschuren, et al.
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of 82
Search research articles
Search
Showing results (711-720 of 818) with videos related to
Sort By:
Page
of 82
Magnetic Resonance in Medicine
|
July 27, 2007
T(1) relaxation in in vivo mouse brain at ultra-high field
Rob C G van de Ven, Bianca Hogers, Arn M J M van den Maagdenberg, et al.
Journal of Lipid Research
|
December 22, 2016
Quantitative profiling of endocannabinoids and related <i>N</i>-acylethanolamines in human CSF using nano LC-MS/MS
Vasudev Kantae, Shinji Ogino, Marek Noga, et al.
The Journal of Clinical Investigation
|
April 3, 2012
Hepatocyte-specific mutation of both NF-κB RelA and STAT3 abrogates the acute phase response in mice
Lee J Quinton, Matthew T Blahna, Matthew R Jones, et al.
Strahlentherapie Und Onkologie : Organ Der Deutschen Rontgengesellschaft ... [Et Al]
|
December 24, 2011
Prospective phase II trial of cetuximab plus VMAT-SIB in locally advanced head and neck squamous cell carcinoma. Feasibility and tolerability in elderly and chemotherapy-ineligible patients
F Alongi, M Bignardi, I Garassino, et al.
Archives of Neurology
|
May 21, 2003
Expanding the phenotypic spectrum of the CACNA1A gene T666M mutation: a description of 5 families with familial hemiplegic migraine
E E Kors, J Haan, N J Giffin, et al.
Neurology
|
August 5, 2018
RVCL-S and CADASIL display distinct impaired vascular function
Irene de Boer, Anine H Stam, Linde Buntinx, et al.
Journal of the American Society for Mass Spectrometry
|
April 17, 2015
Large-scale mass spectrometry imaging investigation of consequences of cortical spreading depression in a transgenic mouse model of migraine
Ricardo J Carreira, Reinald Shyti, Benjamin Balluff, et al.
Neuropediatrics
|
November 10, 2004
Alternating hemiplegia of childhood: no mutations in the second familial hemiplegic migraine gene ATP1A2
E E Kors, K R J Vanmolkot, J Haan, et al.
Cephalalgia : an International Journal of Headache
|
November 25, 2005
The 3p21.1-p21.3 hereditary vascular retinopathy locus increases the risk for Raynaud's phenomenon and migraine
J J Hottenga, K R J Vanmolkot, E E Kors, et al.
Annals of Neurology
|
December 21, 2005
Migraine and MTHFR C677T genotype in a population-based sample
Ann I Scher, Gisela M Terwindt, W M Monique Verschuren, et al.
Page
of 82