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Pediatric Neurology
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January 10, 2026
The Impact of RNA Polymerase III-Related Leukodystrophy on Nonaffected Family Members: A Qualitative Study
Adam Le, Kelly-Ann Thibault, Pouneh Amir Yazdani, et al.
Neurology
|
August 3, 2014
TUBB4A de novo mutations cause isolated hypomyelination
Amy 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 spectrum
Lisa 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-correction
Nicole 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-ABC
Eline M C Hamilton, Enrico Bertini, Luba Kalaydjieva, et al.
Eneuro
|
October 20, 2015
CSF and Blood Levels of GFAP in Alexander Disease
Paige 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 Leukodystrophy
Guy 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 era
Elizabeth 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 era
Elizabeth Wells, Yael Hacohen, Amy Waldman, et al.
Pediatric Neurology
|
May 11, 2020
Phenotypic and Imaging Spectrum Associated With WDR45
Laura A Adang, Amy Pizzino, Alka Malhotra, et al.
Page
of 22
Search research articles
Search
Showing results (131-140 of 217) with videos related to
Sort By:
Page
of 22
Pediatric Neurology
|
January 10, 2026
The Impact of RNA Polymerase III-Related Leukodystrophy on Nonaffected Family Members: A Qualitative Study
Adam Le, Kelly-Ann Thibault, Pouneh Amir Yazdani, et al.
Neurology
|
August 3, 2014
TUBB4A de novo mutations cause isolated hypomyelination
Amy 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 spectrum
Lisa 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-correction
Nicole 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-ABC
Eline M C Hamilton, Enrico Bertini, Luba Kalaydjieva, et al.
Eneuro
|
October 20, 2015
CSF and Blood Levels of GFAP in Alexander Disease
Paige 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 Leukodystrophy
Guy 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 era
Elizabeth 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 era
Elizabeth Wells, Yael Hacohen, Amy Waldman, et al.
Pediatric Neurology
|
May 11, 2020
Phenotypic and Imaging Spectrum Associated With WDR45
Laura A Adang, Amy Pizzino, Alka Malhotra, et al.
Page
of 22