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D Bird

Showing results (641-650 of 780) with videos related to

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The Journal of Physiology|June 10, 2025
Acute intermittent hypercapnic hypoxia augments left ventricular contractilityScott F Thrall, Alex M Williams, Philip J Millar, et al.
Science (New York, N.Y.)|September 16, 1988
Absence of linkage of chromosome 21q21 markers to familial Alzheimer's diseaseG D Schellenberg, T D Bird, E M Wijsman, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|May 18, 2023
Comparison of mild physiological effects of surgical masks and N95 respirators over 60 min at restValerie C Cates, Anthony L Marullo, Rodion Isakovich, et al.
Frontiers in Genetics|November 26, 2020
<i>C9orf72</i> Hexanucleotide Repeat in Huntington-Like Patients: Systematic Review and Meta-AnalysisCarlos Alva-Diaz, Christoper A Alarcon-Ruiz, Kevin Pacheco-Barrios, et al.
Annals of Neurology|September 8, 2000
Familial Alzheimer's disease: site of mutation influences clinical phenotypeC F Lippa, J M Swearer, K J Kane, et al.
Brain : a Journal of Neurology|April 19, 2007
A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathologyJ B Leverenz, C E Yu, T J Montine, et al.
Neurology|March 1, 1990
Transmission and age-at-onset patterns in familial Alzheimer's disease: evidence for heterogeneityL A Farrer, R H Myers, L A Cupples, et al.
Annals of Neurology|November 30, 2005
Prion protein codon 129 genotype prevalence is altered in primary progressive aphasiaXiaohong Li, Lewis P Rowland, Hiroshi Mitsumoto, et al.
Annals of the American Thoracic Society|March 31, 2023
Sex-related Differences in Loop Gain during High-Altitude Sleep-disordered BreathingJordan D Bird, Scott A Sands, Raichel M Alex, et al.
Journal of Huntington'S Disease|October 3, 2017
Enhanced retinal responses in Huntington's disease patientsJocelynn R Pearl, Laura M Heath, Dani E Bergey, et al.
Pageof 78

Showing results (641-650 of 780) with videos related to

Sort By:
Pageof 78
The Journal of Physiology|June 10, 2025
Acute intermittent hypercapnic hypoxia augments left ventricular contractilityScott F Thrall, Alex M Williams, Philip J Millar, et al.
Science (New York, N.Y.)|September 16, 1988
Absence of linkage of chromosome 21q21 markers to familial Alzheimer's diseaseG D Schellenberg, T D Bird, E M Wijsman, et al.
Journal of Applied Physiology (Bethesda, Md. : 1985)|May 18, 2023
Comparison of mild physiological effects of surgical masks and N95 respirators over 60 min at restValerie C Cates, Anthony L Marullo, Rodion Isakovich, et al.
Frontiers in Genetics|November 26, 2020
<i>C9orf72</i> Hexanucleotide Repeat in Huntington-Like Patients: Systematic Review and Meta-AnalysisCarlos Alva-Diaz, Christoper A Alarcon-Ruiz, Kevin Pacheco-Barrios, et al.
Annals of Neurology|September 8, 2000
Familial Alzheimer's disease: site of mutation influences clinical phenotypeC F Lippa, J M Swearer, K J Kane, et al.
Brain : a Journal of Neurology|April 19, 2007
A novel progranulin mutation associated with variable clinical presentation and tau, TDP43 and alpha-synuclein pathologyJ B Leverenz, C E Yu, T J Montine, et al.
Neurology|March 1, 1990
Transmission and age-at-onset patterns in familial Alzheimer's disease: evidence for heterogeneityL A Farrer, R H Myers, L A Cupples, et al.
Annals of Neurology|November 30, 2005
Prion protein codon 129 genotype prevalence is altered in primary progressive aphasiaXiaohong Li, Lewis P Rowland, Hiroshi Mitsumoto, et al.
Annals of the American Thoracic Society|March 31, 2023
Sex-related Differences in Loop Gain during High-Altitude Sleep-disordered BreathingJordan D Bird, Scott A Sands, Raichel M Alex, et al.
Journal of Huntington'S Disease|October 3, 2017
Enhanced retinal responses in Huntington's disease patientsJocelynn R Pearl, Laura M Heath, Dani E Bergey, et al.
Pageof 78