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Christopher M Clark

Showing results (131-140 of 135) with videos related to

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Neurology|August 3, 2012
Plasma multianalyte profiling in mild cognitive impairment and Alzheimer diseaseWilliam T Hu, David M Holtzman, Anne M Fagan, et al.
Archives of Neurology|February 10, 2010
The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegenerationChang-En Yu, Thomas D Bird, Lynn M Bekris, et al.
Archives of Neurology|November 10, 2010
Temporoparietal hypometabolism in frontotemporal lobar degeneration and associated imaging diagnostic errorsKyle B Womack, Ramon Diaz-Arrastia, Howard J Aizenstein, et al.
Nature|July 16, 2025
Global terrestrial nitrogen fixation and its modification by agricultureCarla R Reis Ely, Steven S Perakis, Cory C Cleveland, et al.
The Lancet. Neurology|September 11, 2007
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiativeRosa Rademakers, Matt Baker, Jennifer Gass, et al.
Pageof 14

Showing results (131-140 of 135) with videos related to

Sort By:
Pageof 14
You have reached the last page of results.This site can display upto 135 results.
Neurology|August 3, 2012
Plasma multianalyte profiling in mild cognitive impairment and Alzheimer diseaseWilliam T Hu, David M Holtzman, Anne M Fagan, et al.
Archives of Neurology|February 10, 2010
The spectrum of mutations in progranulin: a collaborative study screening 545 cases of neurodegenerationChang-En Yu, Thomas D Bird, Lynn M Bekris, et al.
Archives of Neurology|November 10, 2010
Temporoparietal hypometabolism in frontotemporal lobar degeneration and associated imaging diagnostic errorsKyle B Womack, Ramon Diaz-Arrastia, Howard J Aizenstein, et al.
Nature|July 16, 2025
Global terrestrial nitrogen fixation and its modification by agricultureCarla R Reis Ely, Steven S Perakis, Cory C Cleveland, et al.
The Lancet. Neurology|September 11, 2007
Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiativeRosa Rademakers, Matt Baker, Jennifer Gass, et al.
Pageof 14