Found: 6
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Transitional Care for Young People with Movement Disorders: Consensus‐Based Recommendations from the MDS Task Force on Pediatrics.
- Published in:
- Movement Disorders Clinical Practice, 2023, v. 10, n. 5, p. 748, doi. 10.1002/mdc3.13728
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- Publication type:
- Article
Deep Brain Stimulation in Progressive Generalized Dystonia in Childhood Associated With ADAR1 Gene Variant.
- Published in:
- Movement Disorders Clinical Practice, 2022, v. 9, p. S29, doi. 10.1002/mdc3.13527
- By:
- Publication type:
- Article
Deep Brain Stimulation in Progressive Generalized Dystonia in Childhood Associated With ADAR1 Gene Variant.
- Published in:
- Movement Disorders Clinical Practice, 2022, v. 9, p. S29, doi. 10.1002/mdc3.13527
- By:
- Publication type:
- Article
The clinical and biochemical hallmarks generally associated with GLUT1DS may be caused by defects in genes other than SLC2A1.
- Published in:
- Clinical Genetics, 2022, v. 102, n. 1, p. 40, doi. 10.1111/cge.14138
- By:
- Publication type:
- Article
Childhood‐Onset Chorea Caused by a Recurrent De Novo DRD2 Variant.
- Published in:
- Movement Disorders, 2021, v. 36, n. 6, p. 1472, doi. 10.1002/mds.28634
- By:
- Publication type:
- Article
Childhood-Onset Chorea Caused by a Recurrent De Novo DRD2 Variant.
- Published in:
- 2021
- By:
- Publication type:
- letter