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W W Shaw

Showing results (171-180 of 177) with videos related to

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Orphanet Journal of Rare Diseases|March 14, 2023
Correction: Ketogenic diet as a glycine lowering therapy in nonketotic hyperglycinemia and impact on brain glycine levelsEmily Shelkowitz, Russell P Saneto, Walla Al-Hertani, et al.
Journal of Medical Genetics|September 13, 2005
AHI1 mutations cause both retinal dystrophy and renal cystic disease in Joubert syndromeM A Parisi, D Doherty, M L Eckert, et al.
Human Molecular Genetics|January 25, 2024
Regional and bilateral MRI and gene signatures in facioscapulohumeral dystrophy: implications for clinical trial design and mechanisms of disease progressionChao-Jen Wong, Seth D Friedman, Lauren Snider, et al.
Biorxiv : the Preprint Server for Biology|March 3, 2023
Validation of the association between MRI and gene signatures in facioscapulohumeral dystrophy muscle: implications for clinical trial designChao-Jen Wong, Seth D Friedman, Lauren Snider, et al.
Stroke|December 18, 2019
Risk of Intracranial Hemorrhage Following Intravenous tPA (Tissue-Type Plasminogen Activator) for Acute Stroke Is Low in ChildrenCatherine Amlie-Lefond, Dennis W W Shaw, Andrew Cooper, et al.
Nature Medicine|November 8, 2016
Fetal brain lesions after subcutaneous inoculation of Zika virus in a pregnant nonhuman primateKristina M Adams Waldorf, Jennifer E Stencel-Baerenwald, Raj P Kapur, et al.
Nature Medicine|February 6, 2018
Congenital Zika virus infection as a silent pathology with loss of neurogenic output in the fetal brainKristina M Adams Waldorf, Branden R Nelson, Jennifer E Stencel-Baerenwald, et al.
Pageof 18

Showing results (171-180 of 177) with videos related to

Sort By:
Pageof 18
You have reached the last page of results.This site can display upto 177 results.
Orphanet Journal of Rare Diseases|March 14, 2023
Correction: Ketogenic diet as a glycine lowering therapy in nonketotic hyperglycinemia and impact on brain glycine levelsEmily Shelkowitz, Russell P Saneto, Walla Al-Hertani, et al.
Journal of Medical Genetics|September 13, 2005
AHI1 mutations cause both retinal dystrophy and renal cystic disease in Joubert syndromeM A Parisi, D Doherty, M L Eckert, et al.
Human Molecular Genetics|January 25, 2024
Regional and bilateral MRI and gene signatures in facioscapulohumeral dystrophy: implications for clinical trial design and mechanisms of disease progressionChao-Jen Wong, Seth D Friedman, Lauren Snider, et al.
Biorxiv : the Preprint Server for Biology|March 3, 2023
Validation of the association between MRI and gene signatures in facioscapulohumeral dystrophy muscle: implications for clinical trial designChao-Jen Wong, Seth D Friedman, Lauren Snider, et al.
Stroke|December 18, 2019
Risk of Intracranial Hemorrhage Following Intravenous tPA (Tissue-Type Plasminogen Activator) for Acute Stroke Is Low in ChildrenCatherine Amlie-Lefond, Dennis W W Shaw, Andrew Cooper, et al.
Nature Medicine|November 8, 2016
Fetal brain lesions after subcutaneous inoculation of Zika virus in a pregnant nonhuman primateKristina M Adams Waldorf, Jennifer E Stencel-Baerenwald, Raj P Kapur, et al.
Nature Medicine|February 6, 2018
Congenital Zika virus infection as a silent pathology with loss of neurogenic output in the fetal brainKristina M Adams Waldorf, Branden R Nelson, Jennifer E Stencel-Baerenwald, et al.
Pageof 18