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Pediatric Neurology
|
March 24, 2009
Newborn screening for Krabbe disease: the New York State model
Patricia K Duffner, Michele Caggana, Joseph J Orsini, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
September 28, 2021
Current directions in tau research: Highlights from Tau 2020
Claire Sexton, Heather Snyder, Dirk Beher, et al.
The Journal of Clinical Investigation
|
January 9, 2019
Loss of the sphingolipid desaturase DEGS1 causes hypomyelinating leukodystrophy
Devesh C Pant, Imen Dorboz, Agatha Schluter, et al.
Molecular Genetics and Metabolism
|
July 3, 2024
Frontiers in congenital disorders of glycosylation consortium, a cross-sectional study report at year 5 of 280 individuals in the natural history cohort
Christina Lam, Fernando Scaglia, Gerard T Berry, et al.
Human Mutation
|
March 1, 2019
SLC35A2-CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported Individuals
Bobby G Ng, Paulina Sosicka, Satish Agadi, et al.
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of 12
Search research articles
Search
Showing results (111-120 of 115) with videos related to
Sort By:
Page
of 12
You have reached the last page of results.
This site can display upto 115 results.
Pediatric Neurology
|
March 24, 2009
Newborn screening for Krabbe disease: the New York State model
Patricia K Duffner, Michele Caggana, Joseph J Orsini, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
September 28, 2021
Current directions in tau research: Highlights from Tau 2020
Claire Sexton, Heather Snyder, Dirk Beher, et al.
The Journal of Clinical Investigation
|
January 9, 2019
Loss of the sphingolipid desaturase DEGS1 causes hypomyelinating leukodystrophy
Devesh C Pant, Imen Dorboz, Agatha Schluter, et al.
Molecular Genetics and Metabolism
|
July 3, 2024
Frontiers in congenital disorders of glycosylation consortium, a cross-sectional study report at year 5 of 280 individuals in the natural history cohort
Christina Lam, Fernando Scaglia, Gerard T Berry, et al.
Human Mutation
|
March 1, 2019
SLC35A2-CDG: Functional characterization, expanded molecular, clinical, and biochemical phenotypes of 30 unreported Individuals
Bobby G Ng, Paulina Sosicka, Satish Agadi, et al.
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of 12