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Glenn W Anderson

Showing results (1-10 of 7) with videos related to

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Biochimica Et Biophysica Acta|December 4, 2012
Human pathology in NCLGlenn W Anderson, Hans H Goebel, Alessandro Simonati
Acta Neuropathologica|February 2, 2012
Neuropathology of neurocutaneous melanosis: histological foci of melanotic neurones and glia may be undetectable on MRIVeronica A Kinsler, Simon M L Paine, Glenn W Anderson, et al.
Journal of Neuroscience Research|January 15, 2016
The Chihuahua dog: A new animal model for neuronal ceroid lipofuscinosis CLN7 disease?Kiterie M E Faller, Jose Bras, Samuel J Sharpe, et al.
Acta Neuropathologica|June 4, 2013
mTOR-dependent abnormalities in autophagy characterize human malformations of cortical development: evidence from focal cortical dysplasia and tuberous sclerosisShireena A Yasin, Abu M Ali, Mathew Tata, et al.
Neurology|July 15, 2016
Diagnosis and misdiagnosis of adult neuronal ceroid lipofuscinosis (Kufs disease)Samuel F Berkovic, John F Staropoli, Stirling Carpenter, et al.
JAMA Ophthalmology|May 26, 2017
Detailed Clinical Phenotype and Molecular Genetic Findings in CLN3-Associated Isolated Retinal DegenerationCristy A Ku, Sarah Hull, Gavin Arno, et al.
Annals of Neurology|October 9, 2018
KCTD7 deficiency defines a distinct neurodegenerative disorder with a conserved autophagy-lysosome defectKyle A Metz, Xinchen Teng, Isabelle Coppens, et al.
Pageof 1

Showing results (1-10 of 7) with videos related to

Sort By:
Pageof 1
Biochimica Et Biophysica Acta|December 4, 2012
Human pathology in NCLGlenn W Anderson, Hans H Goebel, Alessandro Simonati
Acta Neuropathologica|February 2, 2012
Neuropathology of neurocutaneous melanosis: histological foci of melanotic neurones and glia may be undetectable on MRIVeronica A Kinsler, Simon M L Paine, Glenn W Anderson, et al.
Journal of Neuroscience Research|January 15, 2016
The Chihuahua dog: A new animal model for neuronal ceroid lipofuscinosis CLN7 disease?Kiterie M E Faller, Jose Bras, Samuel J Sharpe, et al.
Acta Neuropathologica|June 4, 2013
mTOR-dependent abnormalities in autophagy characterize human malformations of cortical development: evidence from focal cortical dysplasia and tuberous sclerosisShireena A Yasin, Abu M Ali, Mathew Tata, et al.
Neurology|July 15, 2016
Diagnosis and misdiagnosis of adult neuronal ceroid lipofuscinosis (Kufs disease)Samuel F Berkovic, John F Staropoli, Stirling Carpenter, et al.
JAMA Ophthalmology|May 26, 2017
Detailed Clinical Phenotype and Molecular Genetic Findings in CLN3-Associated Isolated Retinal DegenerationCristy A Ku, Sarah Hull, Gavin Arno, et al.
Annals of Neurology|October 9, 2018
KCTD7 deficiency defines a distinct neurodegenerative disorder with a conserved autophagy-lysosome defectKyle A Metz, Xinchen Teng, Isabelle Coppens, et al.
Pageof 1