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- 2023
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Mark
Parkinsonism in Genetic Neurodevelopmental Disorders : A Systematic Review
(
- Contribution to journal › Scientific review
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Mark
Novel Genetic and Phenotypic Expansion in GOSR2-Related Progressive Myoclonus Epilepsy
(
- Contribution to journal › Article
- 2022
-
Mark
Developmental neurobiology of cerebellar and Basal Ganglia connections
(
- Contribution to journal › Article
-
Mark
Serotonergic system in vivo with [11C]DASB PET scans in GTP-cyclohydrolase deficient dopa-responsive dystonia patients
(
- Contribution to journal › Article
-
Mark
Eye movement disorders in inborn errors of metabolism : A quantitative analysis of 37 patients
(
- Contribution to journal › Article
-
Mark
Amino Acid Synthesis Deficiencies
2022) p.453-467(
- Chapter in Book/Report/Conference proceeding › Book chapter
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Mark
Methylation of the serotonin reuptake transporter gene and non-motor symptoms in dystonia patients
(
- Contribution to journal › Article
-
Mark
The Mitochondrial Epigenome : An Unexplored Avenue to Explain Unexplained Myopathies?
(
- Contribution to journal › Article
- 2021
-
Mark
The neurological and neuropsychiatric spectrum of adults with late-treated phenylketonuria
(
- Contribution to journal › Article
-
Mark
Treatment of ARS deficiencies with specific amino acids
(
- Contribution to journal › Article