Mutation of a putative protein degradation gene LITAF/SIMPLE in Charcot-Marie-Tooth disease 1C von STREET, V. A, BENNETT, C. L, GOLDY, J. D, SHIRK, A. J, KLEOPA, K. A, TEMPEL, B. L, LIPE, H. P, SCHERER, S. S, BIRD, T. D, CHANCE, P. F

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The clinical and genetic spectrum of spinocerebellar ataxia 14 von CHEN, D.-H, CIMINO, P. J, WOLFF, J, MORGAN, C, LAU, D, FERNANDEZ, M, SASAKI, H, RASKIND, W. H, BIRD, T. D, RANUM, L. P. W, ZOGHBI, H. Y, YABE, I, SCHUT, L, MARGOLIS, R. L, LIPE, H. P, FELEKE, A, MATSUSHITA, M

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Late-onset hereditary axonal neuropathies von BENNETT, C. L, LAWSON, V. H, BIRD, T. D, BRICKELL, K. L, ISAACS, K, SELTZER, W, LIPE, H. P, WEISS, M. D, CARTER, G. T, FLANIGAN, K. M, CHANCE, P. F

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Charcot–Marie–Tooth neuropathy: clinical phenotypes of four novel mutations in the MPZ and Cx 32 genes von Street, V.A., Meekins, G., Lipe, H.P., Seltzer, W.K., Carter, G.T., Kraft, G.H., Bird, T.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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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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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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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 diseae type 1A von GRAF, W. D, CHANCE, P. F, LENSCH, M. W, ENG, L. J, LIPE, H. P, BIRD, T. D

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

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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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Bisphosphonates for delivering drugs to bone von Sun, Shuting, Tao, Jianguo, Sedghizadeh, Parish P., Cherian, Philip, Junka, Adam F., Sodagar, Esmat, Xing, Lianping, Boeckman, Robert K., Srinivasan, Venkatesan, Yao, Zhenqiang, Boyce, Brendan F., Lipe, Brea, Neighbors, Jeffrey D., Russell, R. Graham G., McKenna, Charles E., Ebetino, Frank H.

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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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Severe renal failure and thrombotic microangiopathy induced by malignant hypertension successfully treated with spironolactone von Villafuerte Ledesma, H.M., Peña Porta, J.M., Iñigo Gil, P., Martin Azara, P., Ruiz Lalglesia, J.E, Tomás LaTorre, A., Martínez Burillo, A., Vernet Perna, P., Álvarez Lipe, R.

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Thermoelectric transfer difference of thermal converters measured with a Josephson source von Burroughs, C.J., Benz, S.P., Hamilton, C.A., Harvey, T.E., Kinard, J.R., Lipe, T.E., Sasaki, H.

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Course of Vascular Access and Relationship with Treatment of Anemia von Portole[Combining Acute Accent]s, Jose[Combining Acute Accent], Lo[Combining Acute Accent]pez-Go[Combining Acute Accent]mez, Juan Manuel, Gruss, Enrique, Aljama, Pedro

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Inaugural Huntington Disease Clinical Research Symposium Organized by the Huntington Study Group von Ross, C. A., Beglinger, L. J., Tomusk, A., Lifer, S., Hastings, S., Dawson, J., Walker, B., Whitlock, K., Johnson, S., Pacifici, Robert, Hersch, S., Katz, Russell, Wheelock, V., Schwartz, G., Mattis, P., Young, P., McArthur, D. L., Chirieac, M. C., Shinaman, A., Shoulson, I., Kane, A. E., Peavy, G. M., Jacobson, M. W., Wasserman, L., Tang, C., Zgaljardic, D., Ma, Y., Dhawan, V., Guttman, M., Eidelberg, D., Peng, S., Rosas, H. D., Gevorkian, S., Oakes, D., Latourelle, J., Fossale, E., Gillis, T., Gusella, J. F., MacDonald, M. E., Myers, R. H., Yastrubetskaya, O., Chiu, E., Goh, A., Kayson, E., Quaid, K., Sims, S., Swenson, M., Harrison, J., Moskowitz, C., Stepanov, N., Suter, G., Johnson, S. A., Nopoulos, P., Beglinger, L., Pierson, R., Lipe, H., Bird, T. D., McCusker, E. A., Lechich, A. J., Duckett, A., Klager, J., Sandler, S., Pae, A., Apostol, B. L., Zuccato, C., Illes, K., Marsh, J. L., Thompson, L. Michels, Patzke, H., Chesworth, R., Li, Z., Rahil, G., Shapiro, G., Leit, S., Beaulieu, P., Fournel, M., Barbier, A., Besterman, J., Deziel, R., Aubeeluck, A., Ross, C., Landwehrmeyer, B., Whitlock, K. B., Lee, J., Kim, R. Y., Cahill, T., Johnson, D., Jacobson, M., Goodman, L. Veatch, Cha, J. H., Adams, M., de Blieck, E. A., McCallum, C., Clarke, A., Stewart, R., Adams, W. H., Paulson, H., Hanson, J. M., Priller, J., Ecker, D.

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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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Tracheal TDx Fetal Lung Maturity Test for Assessing Lung Maturity in Newborns With Respiratory Distress von Giacoia, George P., Lipe, Bill H., Kelly, Cynthia, West, Kerstin

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