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Adeline Vanderver

Showing results (131-140 of 217) with videos related to

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Pediatric Neurology|January 10, 2026
The Impact of RNA Polymerase III-Related Leukodystrophy on Nonaffected Family Members: A Qualitative StudyAdam Le, Kelly-Ann Thibault, Pouneh Amir Yazdani, et al.
Neurology|August 3, 2014
TUBB4A de novo mutations cause isolated hypomyelinationAmy Pizzino, Tyler Mark Pierson, Yiran Guo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2018
Microdeletions excluding YWHAE and PAFAH1B1 cause a unique leukoencephalopathy: further delineation of the 17p13.3 microdeletion spectrumLisa T Emrick, Jill A Rosenfeld, Seema R Lalani, et al.
Annals of Clinical and Translational Neurology|January 23, 2020
Metachromatic leukodystrophy and transplantation: remyelination, no cross-correctionNicole I Wolf, Marjolein Breur, Bonnie Plug, et al.
Neurology|September 22, 2017
<i>UFM1</i> founder mutation in the Roma population causes recessive variant of H-ABCEline M C Hamilton, Enrico Bertini, Luba Kalaydjieva, et al.
Eneuro|October 20, 2015
CSF and Blood Levels of GFAP in Alexander DiseasePaige L Jany, Guillermo E Agosta, William S Benko, et al.
Pediatric Neurology|June 10, 2021
Further Delineation of the Clinical and Pathologic Features of HIKESHI-Related Hypomyelinating LeukodystrophyGuy Helman, Ayelet Zerem, Akshata Almad, et al.
Nature Reviews. Neurology|June 22, 2018
Neuroimmune disorders of the central nervous system in children in the molecular eraElizabeth Wells, Yael Hacohen, Amy Waldman, et al.
Nature Reviews. Neurology|November 17, 2018
Author Correction: Neuroimmune disorders of the central nervous system in children in the molecular eraElizabeth Wells, Yael Hacohen, Amy Waldman, et al.
Pediatric Neurology|May 11, 2020
Phenotypic and Imaging Spectrum Associated With WDR45Laura A Adang, Amy Pizzino, Alka Malhotra, et al.
Pageof 22

Showing results (131-140 of 217) with videos related to

Sort By:
Pageof 22
Pediatric Neurology|January 10, 2026
The Impact of RNA Polymerase III-Related Leukodystrophy on Nonaffected Family Members: A Qualitative StudyAdam Le, Kelly-Ann Thibault, Pouneh Amir Yazdani, et al.
Neurology|August 3, 2014
TUBB4A de novo mutations cause isolated hypomyelinationAmy Pizzino, Tyler Mark Pierson, Yiran Guo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 21, 2018
Microdeletions excluding YWHAE and PAFAH1B1 cause a unique leukoencephalopathy: further delineation of the 17p13.3 microdeletion spectrumLisa T Emrick, Jill A Rosenfeld, Seema R Lalani, et al.
Annals of Clinical and Translational Neurology|January 23, 2020
Metachromatic leukodystrophy and transplantation: remyelination, no cross-correctionNicole I Wolf, Marjolein Breur, Bonnie Plug, et al.
Neurology|September 22, 2017
<i>UFM1</i> founder mutation in the Roma population causes recessive variant of H-ABCEline M C Hamilton, Enrico Bertini, Luba Kalaydjieva, et al.
Eneuro|October 20, 2015
CSF and Blood Levels of GFAP in Alexander DiseasePaige L Jany, Guillermo E Agosta, William S Benko, et al.
Pediatric Neurology|June 10, 2021
Further Delineation of the Clinical and Pathologic Features of HIKESHI-Related Hypomyelinating LeukodystrophyGuy Helman, Ayelet Zerem, Akshata Almad, et al.
Nature Reviews. Neurology|June 22, 2018
Neuroimmune disorders of the central nervous system in children in the molecular eraElizabeth Wells, Yael Hacohen, Amy Waldman, et al.
Nature Reviews. Neurology|November 17, 2018
Author Correction: Neuroimmune disorders of the central nervous system in children in the molecular eraElizabeth Wells, Yael Hacohen, Amy Waldman, et al.
Pediatric Neurology|May 11, 2020
Phenotypic and Imaging Spectrum Associated With WDR45Laura A Adang, Amy Pizzino, Alka Malhotra, et al.
Pageof 22