P036Exploring us obstetrician-gynecologists’ characterization of periviable pregnancy-ending interventions: A mixed methods study by Flink-Bochacki, R, McLeod, C, Lipe, H, Rapkin, RB, Rubin, S, Heuser, C

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Charcot–Marie–Tooth neuropathy: clinical phenotypes of four novel mutations in the MPZ and Cx 32 genes by Street, V.A., Meekins, G., Lipe, H.P., Seltzer, W.K., Carter, G.T., Kraft, G.H., Bird, T.D.

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Familial Aggregation of Psychotic Symptoms in Huntington's Disease by Tsuang, Debby, Almqvist, Elisabeth W., Lipe, Hillary, Strgar, Franc, DiGiacomo, Lilly, Hoff, David, Eugenio, Charisma, Hayden, Michael R., Bird, Thomas D.

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Missense Mutations in the Regulatory Domain of PKCγ: A New Mechanism for Dominant Nonepisodic Cerebellar Ataxia by 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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Late-Onset Huntington’s Disease: A Review of 41 Cases by Lipe, H., Bird, T.D.

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

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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 by Raskind, Wendy H., Pericak-Vance, Margaret A., Lennon, Felicia, Wolff, John, Lipe, Hillary P., Bird, Thomas D.

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Familial dyskinesia and facial myokymia (FDFM): A novel movement disorder by Fernandez, Magali, Raskind, Wendy, Wolff, John, Matsushita, Mark, Yuen, Eric, Graf, William, Lipe, Hillary, Bird, Thomas

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

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Further localization of a gene for paroxysmal dystonic choreoathetosis to a 5-cM region on chromosome 2q34 by RASKIND, W. H, BOLIN, T, WOLFF, J, FINK, J, MATSUSHITA, M, LITT, M, LIPE, H, BIRD, T. D

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Inaugural Huntington Disease Clinical Research Symposium Organized by the Huntington Study Group by 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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Familial aggregation of schizophrenia-like symptoms in huntington's disease by Tsuang, Debby, DiGiacomo, Lilly, Lipe, Hillary, Bird, Thomas D.

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

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A reevaluation of the NIST low-frequency standards for AC-DC difference in the voltage range 0.6-100 V by Lipe, T.E.

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Severe vincristine neuropathy in Charcot-Marie-Tooth diseae type 1A by GRAF, W. D, CHANCE, P. F, LENSCH, M. W, ENG, L. J, LIPE, H. P, BIRD, T. D

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Genetic linkage and heterogenity in type I charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I) by CHANCE, P. F, BIRD, T. D, O'CONNELL, P, LIPE, H, LALOUEL, J.-M, LEPPERT, M

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Immune checkpoint inhibitor-associated myasthenia gravis, myositis, and myocarditis overlap syndrome by Lipe, Demis N., Galvis-Carvajal, Elkin, Rajha, Eva, Wechsler, Adriana H., Gaeta, Susan

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EHRA/EAPCI expert consensus statement on catheter-based left atrial appendage occlusion by Meier, Bernhard, Blaauw, Yuri, Khattab, Ahmed A, Lewalter, Torsten, Sievert, Horst, Tondo, Claudio, Glikson, Michael

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Cardiotoxicity associated with immune checkpoint inhibitors and CAR T-cell therapy by Lipe, Demis N., Rajha, Eva, Wechsler, Adriana H., Gaeta, Susan, Palaskas, Nicolas L., Alhajji, Zahra, Viets-Upchurch, Jayne, Chaftari, Patrick

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Evaluation and management of acute high-grade immunotherapy-related neurotoxicity by Sandoval, Marcelo, Wechsler, Adriana H., Alhajji, Zahra, Viets-Upchurch, Jayne, Brock, Patricia, Lipe, Demis N., Al-breiki, Aisha, Yeung, Sai-Ching J.

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