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Cerebellum (London, England)|August 24, 2012
Spinocerebellar ataxia type 7: clinical course, phenotype-genotype correlations, and neuropathologyLaura C Horton, Matthew P Frosch, Mark G Vangel, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|August 14, 1998
A unique familial leukodystrophy with adult onset dementia and abnormal glycolipid storage: a new lysosomal disease?D K Simon, M L Rodriguez, M P Frosch, et al.
Neurobiology of Disease|April 7, 2007
Effects of gender on nigral gene expression and parkinson diseaseIppolita Cantuti-Castelvetri, Christine Keller-McGandy, Bérengère Bouzou, et al.
Acta Neuropathologica Communications|October 22, 2014
Frequent and symmetric deposition of misfolded tau oligomers within presynaptic and postsynaptic terminals in Alzheimer's diseaseHwan-Ching Tai, Bo Y Wang, Alberto Serrano-Pozo, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|March 18, 2005
Familial Alzheimer's disease presenilin 1 mutations cause alterations in the conformation of presenilin and interactions with amyloid precursor proteinOksana Berezovska, Alberto Lleo, Lauren D Herl, et al.
The American Journal of Tropical Medicine and Hygiene|October 30, 2020
Antibody Profiles to P. falciparum Antigens Over Time Characterize Acute and Long-Term Malaria Exposure in an Area of Low and Unstable TransmissionBartholomew N Ondigo, Karen E S Hamre, Anne E P Frosch, et al.
The American Journal of Clinical Nutrition|August 1, 2014
Decline in childhood iron deficiency after interruption of malaria transmission in highland KenyaAnne E P Frosch, Bartholomew N Ondigo, George A Ayodo, et al.
Frontiers in Neuroanatomy|February 27, 2023
Pentad: A reproducible cytoarchitectonic protocol and its application to parcellation of the human hippocampusEmily M Williams, Emma W Rosenblum, Nicole Pihlstrom, et al.
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