Novel Mutations in CLN5 of Chinese Patients With Neuronal Ceroid Lipofuscinosis.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Works matching IS 08830738 AND DT 2018 AND VI 33 AND IP 13
Results: 10
1
2
JCN Calendar of Events.
- Published in:
- 2018
- Publication type:
- Calendar
3
Evolution of Brain Glucose Metabolic Abnormalities in Children With Epilepsy and SCN1A Gene Variants.
- Published in:
- Journal of Child Neurology, 2018, v. 33, n. 13, p. 832, doi. 10.1177/0883073818796373
- By:
- Publication type:
- Article
4
Corrigendum.
- Published in:
- 2018
- Publication type:
- Correction Notice
5
Current Therapeutic Approaches in Leukodystrophies: A Review.
- Published in:
- Journal of Child Neurology, 2018, v. 33, n. 13, p. 861, doi. 10.1177/0883073818792313
- By:
- Publication type:
- Article
6
Neurology Q&A Review.
- Published in:
- 2018
- By:
- Publication type:
- Book Review
7
ST3GAL5-Related Disorders: A Deficiency in Ganglioside Metabolism and a Genetic Cause of Intellectual Disability and Choreoathetosis.
- Published in:
- Journal of Child Neurology, 2018, v. 33, n. 13, p. 825, doi. 10.1177/0883073818791099
- By:
- Publication type:
- Article
8
Multiple Sulfatase Deficiency: A Case Series With a Novel Mutation.
- Published in:
- Journal of Child Neurology, 2018, v. 33, n. 13, p. 820, doi. 10.1177/0883073818790851
- By:
- Publication type:
- Article
9
A Case of Mercury Toxicity Complicated by Acute Inflammatory Demyelinating Polyneuropathy.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
10
Imaging Brain Metabolism in the Newborn.
- Published in:
- Journal of Child Neurology, 2018, v. 33, n. 13, p. 851, doi. 10.1177/0883073818792308
- By:
- Publication type:
- Article