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JNNP 84:748-755, Hacohen, Y.,et al, 2013
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Neurol 73:430-437, Verhagen,M.M.M.,et al, 2009
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Neurol 68:1710-1717, Langbehn,D.R.,et al, 2007
Saccades in Presymptomatic and Early Stages of Huntington Disease
Neurol 67:394-399, Blekher,T.,et al, 2006
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Neurol 67:485-487, Golding,C.V.P.,et al, 2006
Functional Brain Changes in Presymptomatic Hunington's Disease
Ann Neurol 55:879-883, Reading,S.A.,et al, 2004
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Pediatrics 113:883-886, Kurlan,R. &Kaplan,E., 2004
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JNNP 69: 5-12, Gray,R.G.F. et al, 2000
Family History and DNA Analysis in Patients With Suspected Huntington's Disease
JNNP 69:54-59, Siesling,S. et al, 2000
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Neurol 51:215-220, Rosenblatt,A.,et al, 1998
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JNNP 65:436-445, Janavs,J.L.&Aminoff,M.J., 1998
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Neurol 49:1048-1053, Nance,M.A.,et al, 1997
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Neurol 47:1578-1580, Nance,M.A.,et al, 1996
Hereditary Late-Onset Chorea Without Significant Dementia:Genetic Evid for Phenotypic Variation in Huntington's Disease
Neurol 45:443-447, Britton,J.W.,et al, 1995
Psychosis as the Initial Manifestation of Adult-Onset Niemann-Pick Disease Type C
Neurol 45:1739-1743, Shulman,L.M.,et al, 1995
A Worldwide Study of the Huntington's Disease Mutation, The Sensitivity & Specificity of Measuring CAG Repeats
NEJM 330:1401-1406, 14501994., Kremer,B.,et al, 1994
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Lancet 344:714-717, Davis,M.B.,et al, 1994
Trinucleotide Repeat Expansion in Neurological Disease
Ann Neurol 36:814-822, LaSpada,A.R.,et al, 1994
Clinical Consequences of Isolating the Gene for Huntington's Disease
BMJ 307:397-398, Harper,P.S., 1993
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Ann Neurol 34:757-773, Martin,J.B., 1993
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Ann Neurol 31:293-298, Bateman,D.,et al, 1992
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JNNP 55:692-696, Walshe,J.M.&Yealland,M., 1992
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JAMA 268:1451-1453, Lockshin,M.D., 1992
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