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A Schultz

Showing results (841-850 of 867) with videos related to

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The Lancet. Neurology|July 29, 2024
γ-Secretase activity, clinical features, and biomarkers of autosomal dominant Alzheimer's disease: cross-sectional and longitudinal analysis of the Dominantly Inherited Alzheimer Network observational study (DIAN-OBS)Stephanie A Schultz, Lei Liu, Aaron P Schultz, et al.
Journal of AOAC International|July 9, 2005
Evaluation of the VIDAS Listeria (LIS) immunoassay for the detection of Listeria in foods using demi-Fraser and Fraser enrichment broths, as modification of AOAC Official Method 999.06 (AOAC Official Method 2004.06)Karen M Silbernagel, Robert P Jechorek, Amanda L Kaufer, et al.
Nature Medicine|January 22, 2019
Serum neurofilament dynamics predicts neurodegeneration and clinical progression in presymptomatic Alzheimer's diseaseOliver Preische, Stephanie A Schultz, Anja Apel, et al.
Ecology Letters|January 27, 2021
The influence of vector-borne disease on human history: socio-ecological mechanismsTejas S Athni, Marta S Shocket, Lisa I Couper, et al.
Molecular Neurodegeneration|December 19, 2023
Advanced structural brain aging in preclinical autosomal dominant Alzheimer diseasePeter R Millar, Brian A Gordon, Julie K Wisch, et al.
Sensors (Basel, Switzerland)|May 11, 2024
Nanoscale Three-Dimensional Imaging of Integrated Circuits Using a Scanning Electron Microscope and Transition-Edge Sensor SpectrometerNathan Nakamura, Paul Szypryt, Amber L Dagel, et al.
Nature Communications|November 18, 2024
Comparative neurofilament light chain trajectories in CSF and plasma in autosomal dominant Alzheimer's diseaseAnna Hofmann, Lisa M Häsler, Marius Lambert, et al.
Human Mutation|February 1, 2012
Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic featuresAllen N Lamb, Jill A Rosenfeld, Nicholas J Neill, et al.
The Lancet. Neurology|January 22, 2022
Variant-dependent heterogeneity in amyloid β burden in autosomal dominant Alzheimer's disease: cross-sectional and longitudinal analyses of an observational studyJasmeer P Chhatwal, Stephanie A Schultz, Eric McDade, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 26, 2025
BiomarkersJulie K Wisch, Nicole S McKay, Matthew D Zammit, et al.
Pageof 87

Showing results (841-850 of 867) with videos related to

Sort By:
Pageof 87
The Lancet. Neurology|July 29, 2024
γ-Secretase activity, clinical features, and biomarkers of autosomal dominant Alzheimer's disease: cross-sectional and longitudinal analysis of the Dominantly Inherited Alzheimer Network observational study (DIAN-OBS)Stephanie A Schultz, Lei Liu, Aaron P Schultz, et al.
Journal of AOAC International|July 9, 2005
Evaluation of the VIDAS Listeria (LIS) immunoassay for the detection of Listeria in foods using demi-Fraser and Fraser enrichment broths, as modification of AOAC Official Method 999.06 (AOAC Official Method 2004.06)Karen M Silbernagel, Robert P Jechorek, Amanda L Kaufer, et al.
Nature Medicine|January 22, 2019
Serum neurofilament dynamics predicts neurodegeneration and clinical progression in presymptomatic Alzheimer's diseaseOliver Preische, Stephanie A Schultz, Anja Apel, et al.
Ecology Letters|January 27, 2021
The influence of vector-borne disease on human history: socio-ecological mechanismsTejas S Athni, Marta S Shocket, Lisa I Couper, et al.
Molecular Neurodegeneration|December 19, 2023
Advanced structural brain aging in preclinical autosomal dominant Alzheimer diseasePeter R Millar, Brian A Gordon, Julie K Wisch, et al.
Sensors (Basel, Switzerland)|May 11, 2024
Nanoscale Three-Dimensional Imaging of Integrated Circuits Using a Scanning Electron Microscope and Transition-Edge Sensor SpectrometerNathan Nakamura, Paul Szypryt, Amber L Dagel, et al.
Nature Communications|November 18, 2024
Comparative neurofilament light chain trajectories in CSF and plasma in autosomal dominant Alzheimer's diseaseAnna Hofmann, Lisa M Häsler, Marius Lambert, et al.
Human Mutation|February 1, 2012
Haploinsufficiency of SOX5 at 12p12.1 is associated with developmental delays with prominent language delay, behavior problems, and mild dysmorphic featuresAllen N Lamb, Jill A Rosenfeld, Nicholas J Neill, et al.
The Lancet. Neurology|January 22, 2022
Variant-dependent heterogeneity in amyloid β burden in autosomal dominant Alzheimer's disease: cross-sectional and longitudinal analyses of an observational studyJasmeer P Chhatwal, Stephanie A Schultz, Eric McDade, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|December 26, 2025
BiomarkersJulie K Wisch, Nicole S McKay, Matthew D Zammit, et al.
Pageof 87