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CHRISTINE B HUNTER

TitleInstructor
InstitutionBaylor College of Medicine
DepartmentDepartment of Neurology
DivisionNeurology
Address7200 Cambridge Street, M.S. BCM609
9th Floor, Suite 9A
Houston TX 77030
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    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    1. A randomized clinical trial of high-dosage coenzyme Q10 in early Parkinson disease: no evidence of benefit. JAMA Neurol. 2014 May; 71(5):543-52. PMID: 24664227.
      View in: PubMed
    2. Pulliam CL, Eichenseer SR, Goetz CG, Waln O, Hunter CB, Jankovic J, Vaillancourt DE, Giuffrida JP, Heldman DA. Continuous in-home monitoring of essential tremor. Parkinsonism Relat Disord. 2014 Jan; 20(1):37-40. PMID: 24126021; PMCID: PMC3946846.
    3. Deng H, Le WD, Hunter CB, Mejia N, Xie WJ, Jankovic J. A family with Parkinson disease, essential tremor, bell palsy, and parkin mutations. Arch Neurol. 2007 Mar; 64(3):421-4. PMID: 17353387.
      View in: PubMed
    4. Deng H, Le W, Guo Y, Hunter CB, Xie W, Huang M, Jankovic J. Genetic analysis of LRRK2 mutations in patients with Parkinson disease. J Neurol Sci. 2006 Dec 21; 251(1-2):102-6. PMID: 17097110.
      View in: PubMed
    5. Ondo WG, Mejia NI, Hunter CB. A pilot study of the clinical efficacy and safety of memantine for Huntington's disease. Parkinsonism Relat Disord. 2007 Oct; 13(7):453-4. PMID: 17046312.
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    6. Deng H, Le WD, Hunter CB, Ondo WG, Guo Y, Xie WJ, Jankovic J. Heterogeneous phenotype in a family with compound heterozygous parkin gene mutations. Arch Neurol. 2006 Feb; 63(2):273-7. PMID: 16476817.
      View in: PubMed
    7. Deng H, Le W, Guo Y, Hunter CB, Xie W, Jankovic J. Genetic and clinical identification of Parkinson's disease patients with LRRK2 G2019S mutation. Ann Neurol. 2005 Jun; 57(6):933-4. PMID: 15929036.
      View in: PubMed
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