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Zanni

Showing results (701-710 of 943) with videos related to

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Physical Therapy|March 17, 2012
Neuromuscular electrical stimulation for intensive care unit-acquired weakness: protocol and methodological implications for a randomized, sham-controlled, phase II trialMichelle E Kho, Alexander D Truong, Roy G Brower, et al.
Cerebellum (London, England)|March 6, 2019
Correction to: Biallelic Variants in the Nuclear Pore Complex Protein NUP93 Are Associated with Non-progressive Congenital AtaxiaGinevra Zanni, P De Magistris, M Nardella, et al.
AIDS (London, England)|March 3, 2017
Effects of pitavastatin and pravastatin on markers of immune activation and arterial inflammation in HIVMabel Toribio, Kathleen V Fitch, Laura Sanchez, et al.
Scientific Reports|September 17, 2017
Influenza D in Italy: towards a better understanding of an emerging viral infection in swineEmanuela Foni, Chiara Chiapponi, Laura Baioni, et al.
Neurogenetics|October 2, 2009
A novel mutation in the DLG3 gene encoding the synapse-associated protein 102 (SAP102) causes non-syndromic mental retardationGinevra Zanni, Hilde van Esch, Anissa Bensalem, et al.
The Journal of Physical Chemistry. B|August 16, 2021
Application of 2D IR Bioimaging: Hyperspectral Images of Formalin-Fixed Pancreatic Tissues and Observation of Slow Protein DegradationSidney S Dicke, Ariel M Alperstein, Kathryn L Schueler, et al.
Open Forum Infectious Diseases|July 12, 2017
Aspartame Intake Relates to Coronary Plaque Burden and Inflammatory Indices in Human Immunodeficiency VirusLeangelo N Hall, Laura R Sanchez, Jane Hubbard, et al.
Neurology|October 14, 2005
Oligophrenin 1 mutations frequently cause X-linked mental retardation with cerebellar hypoplasiaG Zanni, Y Saillour, M Nagara, et al.
Neurology|January 24, 2020
Age and sex prevalence estimate of Joubert syndrome in ItalySara Nuovo, Ilaria Bacigalupo, Monia Ginevrino, et al.
International Journal of Molecular Sciences|June 2, 2021
Novel <i>KCND3</i> Variant Underlying Nonprogressive Congenital Ataxia or SCA19/22 Disrupt K<sub>V</sub>4.3 Protein Expression and K+ Currents with Variable Effects on Channel PropertiesGinevra Zanni, Cheng-Tsung Hsiao, Ssu-Ju Fu, et al.
Pageof 95

Showing results (701-710 of 943) with videos related to

Sort By:
Pageof 95
Physical Therapy|March 17, 2012
Neuromuscular electrical stimulation for intensive care unit-acquired weakness: protocol and methodological implications for a randomized, sham-controlled, phase II trialMichelle E Kho, Alexander D Truong, Roy G Brower, et al.
Cerebellum (London, England)|March 6, 2019
Correction to: Biallelic Variants in the Nuclear Pore Complex Protein NUP93 Are Associated with Non-progressive Congenital AtaxiaGinevra Zanni, P De Magistris, M Nardella, et al.
AIDS (London, England)|March 3, 2017
Effects of pitavastatin and pravastatin on markers of immune activation and arterial inflammation in HIVMabel Toribio, Kathleen V Fitch, Laura Sanchez, et al.
Scientific Reports|September 17, 2017
Influenza D in Italy: towards a better understanding of an emerging viral infection in swineEmanuela Foni, Chiara Chiapponi, Laura Baioni, et al.
Neurogenetics|October 2, 2009
A novel mutation in the DLG3 gene encoding the synapse-associated protein 102 (SAP102) causes non-syndromic mental retardationGinevra Zanni, Hilde van Esch, Anissa Bensalem, et al.
The Journal of Physical Chemistry. B|August 16, 2021
Application of 2D IR Bioimaging: Hyperspectral Images of Formalin-Fixed Pancreatic Tissues and Observation of Slow Protein DegradationSidney S Dicke, Ariel M Alperstein, Kathryn L Schueler, et al.
Open Forum Infectious Diseases|July 12, 2017
Aspartame Intake Relates to Coronary Plaque Burden and Inflammatory Indices in Human Immunodeficiency VirusLeangelo N Hall, Laura R Sanchez, Jane Hubbard, et al.
Neurology|October 14, 2005
Oligophrenin 1 mutations frequently cause X-linked mental retardation with cerebellar hypoplasiaG Zanni, Y Saillour, M Nagara, et al.
Neurology|January 24, 2020
Age and sex prevalence estimate of Joubert syndrome in ItalySara Nuovo, Ilaria Bacigalupo, Monia Ginevrino, et al.
International Journal of Molecular Sciences|June 2, 2021
Novel <i>KCND3</i> Variant Underlying Nonprogressive Congenital Ataxia or SCA19/22 Disrupt K<sub>V</sub>4.3 Protein Expression and K+ Currents with Variable Effects on Channel PropertiesGinevra Zanni, Cheng-Tsung Hsiao, Ssu-Ju Fu, et al.
Pageof 95