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- 2015
-
Mark
A novel diagnostic approach to patients with myoclonus
(
- Contribution to journal › Scientific review
-
Mark
Myoclonus in childhood-onset neurogenetic disorders : The importance of early identification and treatment
(
- Contribution to journal › Article
- 2014
-
Mark
Rare inborn errors of metabolism with movement disorders : a case study to evaluate the impact upon quality of life and adaptive functioning
(
- Contribution to journal › Article
-
Mark
Assessment of speech in early-onset ataxia : A pilot study
(
- Contribution to journal › Article
-
Mark
Ramsay hunt syndrome : Clinical characterization of progressive myoclonus ataxia caused by GOSR2 mutation
(
- Contribution to journal › Article
- 2012
-
Mark
Neurodegeneration with brain iron accumulation on MRI : An adult case of α-mannosidosis
(
- Chapter in Book/Report/Conference proceeding › Book chapter