Cortical Myoclonus in a Young Boy with GOSR2 Mutation Mimics Chorea

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MOVEMENT DISORDERS CLINICAL PRACTICE (ELECTRONIC), Vol. 2, Iss. 1, 2015-03 ,pp. : 61-63

John Wiley & Sons Inc

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SPG11 Mutations Associated With a Complex Phenotype Resembling Dopa‐Responsive Dystonia

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MOVEMENT DISORDERS CLINICAL PRACTICE (ELECTRONIC), Vol. 2, Iss. 2, 2015-06 ,pp. : 149-154

John Wiley & Sons Inc

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Myoclonus, Epilepsy, and Ataxia Resulting From Potassium Channel Gene Mutation: Expanding the Spectrum Underlying Ramsay Hunt Syndrome

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MOVEMENT DISORDERS CLINICAL PRACTICE (ELECTRONIC), Vol. 2, Iss. 3, 2015-09 ,pp. : 230-231

John Wiley & Sons Inc

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Adult‐Onset Focal Chorea in Fahr's Disease Resulting From SLC20A2 Mutation: A Novel Phenotype

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MOVEMENT DISORDERS CLINICAL PRACTICE (ELECTRONIC), Vol. 2, Iss. 1, 2015-03 ,pp. : 79-80

John Wiley & Sons Inc

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Prenatal and neonatal risk factors associated with children's developmental status at ages 4–7: lessons from the Jiangsu China birth defects prevention cohort

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CHILD: CARE, HEALTH AND DEVELOPMENT, Vol. 41, Iss. 5, 2015-09 ,pp. : 712-721

John Wiley & Sons Inc

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