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- 2018
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Mark
Progressive myoclonus ataxia : Time for a new definition?
(
- Contribution to journal › Article
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Mark
Reversal of status dystonicus after relocation of pallidal electrodes in DYT6 generalized dystonia
(
- Contribution to journal › Article
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Mark
Expanding the ADCY5 phenotype toward spastic paraparesis : Amutation in the M2 domain
(
- Contribution to journal › Article
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Mark
A preliminary study of telemedicine for patients with hepatic glycogen storage disease and their healthcare providers : from bedside to home site monitoring
(
- Contribution to journal › Article
-
Mark
Fever-Induced Paroxysmal Weakness and Encephalopathy (FIPWE)—Part of a Phenotypic Continuum in Patients With ATP1A3 Mutations?
(
- Contribution to journal › Letter
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Mark
Treatable inherited rare movement disorders
(
- Contribution to journal › Scientific review
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Mark
Ketogenic Diet in Refractory Childhood Epilepsy : Starting With a Liquid Formulation in an Outpatient Setting
(
- Contribution to journal › Article
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Mark
Crossing barriers : a multidisciplinary approach to children and adults with young-onset movement disorders
(
- Contribution to journal › Article
- 2017
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Mark
Dystonia-deafness syndrome caused by a β-actin gene mutation and response to deep brain stimulation
(
- Contribution to journal › Debate/Note/Editorial
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Mark
Quality of life of Hurler syndrome patients after successful hematopoietic stem cell transplantation
(
- Contribution to journal › Article