Cerebral cavernous malformation: novel mutation in a Chinese family and evidence for heterogeneity von Chen, Dong-Hui, Lipe, Hillary P., Qin, Zhen, Bird, Thomas D.

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The Consequences of Testing for Huntington's Disease von Bird, T D, Bennett, R L, Lipe, H P

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Severe vincristine neuropathy in charcot‐marie‐tooth disease type 1A von Graf, William D., Chance, Phillip F., Lensch, M. William, Eng, Lilly J., Lipe, Hillary P., Bird, Thomas D.

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Clinical and pathological phenotype of the original family with Charcot-Marie-Tooth type 1B: A 20-year study von Bird, Thomas D., Kraft, George H., Lipe, Hillary P., Kenney, Kimbra L., Sumi, S. Mark

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Moving the Patient in Bed: Effects on Intracranial Pressure von MITCHELL, PAMELA H, OZUNA, JUDITH, LIPE, HILLARY P

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Familial spastic paraparesis: Evaluation of locus heterogeneity, anticipation, and haplotype mapping of the SPG4 locus on the short arm of chromosome 2 von Raskind, Wendy H., Pericak-Vance, Margaret A., Lennon, Felicia, Wolff, John, Lipe, Hillary P., Bird, Thomas D.

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Charcot-Marie-Tooth type IA with 17p11.2–12 duplication predisposes to severe vincristine neuropathy von Graf, William D., Chance, Phillip F., Lensch, William, Eng, Lily J., Lipe, Hillary P., Bird, Thomas D.

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The Function of Weeping in the Adult von Lipe, Hillary P.

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Letters von Smith, Margaret, MacAuley, Cecelia, Stephany, Theresa, David, Janis H., Cooke, Richard W., Johnston, Linda, Wilkinson, Olive F., Dreves, Katharine, Zakul, Ilene, Lipe, Hillary P., Wheat, Margaret, Thomas, Betty, Cooper, Signe S., Garcia, Marjorie S., Prock, Valencia N., Trautman, Mary Jane, Brown, Amy Frances, Lamberton, Martha M., Winter, Melinda G., Kelly, Joyce W., Shockey, Carol, Scott, Kathryn Kelley, Goldstein, Nancy, Richter, Lucretia

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Missense Mutations in the Regulatory Domain of PKCγ: A New Mechanism for Dominant Nonepisodic Cerebellar Ataxia von Chen, Dong-Hui, Brkanac, Zoran, Christophe Verlinde, L.M.J., Tan, Xiao-Jian, Bylenok, Laura, Nochlin, David, Matsushita, Mark, Lipe, Hillary, Wolff, John, Fernandez, Magali, Cimino, P.J., Thomas Bird, D., Raskind, Wendy H.

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Challenges assessing clinical endpoints in early Huntington disease von Paulsen, Jane S., Wang, Chiachi, Duff, Kevin, Barker, Roger, Nance, Martha, Beglinger, Leigh, Moser, David, Williams, Janet K., Simpson, Sheila, Langbehn, Douglas, van Kammen, Daniel P.

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Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I) von Chance, P F, Bird, T D, O'Connell, P, Lipe, H, Lalouel, J M, Leppert, M

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