Statins and the neuromuscular system: a neurologist's perspective von Argov, Z.

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EFNS/ENS Guidelines for the treatment of ocular myasthenia von Kerty, E., Elsais, A., Argov, Z., Evoli, A., Gilhus, N. E.

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T.I.2 von Argov, Z

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IN58-TH-02 Hereditary inclusions body myopathies (HIBM) von Argov, Z

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Characterization of Blood Glucose & Glycosuria following IV Trehalose (Cabaletta) administration for OPMD von Vornovitzki, H, Blotnick, S, Gliko-Kabir, I, Argov, Z, Caraco, Y

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T.I.2: Therapeutic efforts in GNE myopathy von Argov, Z.

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Treatment of human myasthenia gravis with oral antisense suppression of acetylcholinesterase von ARGOV, Z, MCKEE, D, AGUS, S, BRAWER, S, SHLOMOWITZ, N, BEN YOSEPH, O, SOREQ, H, SUSSMAN, J. D

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Hereditary inclusion body myopathy: The Middle Eastern genetic cluster von ARGOV, Z, EISENBERG, I, GRABOV-NARDINI, G, SADEH, M, WIRGUIN, I, SOFFER, D, MITRANI-ROSENBAUM, S

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P.3.4 In vivo GNE interactions von Argov, Z, Harazi, A, Becker Cohen, M, Hinderlich, S, Mitrani Rosenbaum, S

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G.O.27 von Lau, H, Argov, Z, Caraco, Y, Pestronk, A, Shieh, P, Skrinar, A.M, Mayhew, J, Martinisi, J, Kakkis, E

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G.P.55 von Mitrani-Rosenbaum, S, Yakovlev, L, Cohen, M. Becker, Rivni, O, Harazi, A, Noguchi, S, Nishino, I, Fellig, Y, Argov, Z

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Congenital myasthenic syndromes in Israel: Genetic and clinical characterization von Aharoni, S, Sadeh, M, Sagi, L, Rabie, M, Daana, M, Argov, Z, Edvardson, S, Shapira, Y, Dor, T, Bloch, A, Engel, A, Nevo, Y

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G.P.153 von Tajsharghi, H, Hammans, S, Lindberg, C, Lossos, A, Clarke, N.F, Mazanti, I, Waddell, L.B, Fellig, Y, Foulds, N, Katifi, H, Raheem, O, Udd, B, Argov, Z, Oldfors, A

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Dysferlin is a Plasma Membrane Protein and is Expressed Early in Human Development von Anderson, Louise V. B., Davison, Keith, Moss, Jennifer A., Young, Carol, Cullen, Michael J., Walsh, John, Johnson, Margaret A., Bashir, Rumaisa, Britton, Stephen, Keers, Sharon, Argov, Zohar, Mahjneh, Ibrahim, Fougerousse, Françoise, Beckmann, Jacques S., Bushby, Kate M. D.

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P2.01 Phenotypic variability of knock in mice carrying the M712T mutation in GNE von Salama, I, Argov, Z, Mitrani-Rosenbaum, S

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GNE protein expression and subcellular distribution are unaltered in HIBM von KRAUSE, S, ALEO, A, HINDERLICH, S, MERLINI, L, TOURNEV, I, WALTER, M. C, ARGOV, Z, MITRANI-ROSENBAUM, S, LOCHMÜLLER, H

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68P Induced muscle and liver absence of Gne in postnatal mice does not result in structural or functional muscle impairment von Mitrani-Rosenbaum, S., Harazi, A., Yakovlev, L., Ilouz, N., Selke, P., Horstkorte, R., Argov, Z.

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P4.47 Hereditary inclusion body myopathy therapy: Assessment of an adeno associated virus AAV2/8 based GNE gene delivery system von Mitrani-Rosenbaum, S, Yakovlev, L, Becker-Cohen, M, Felig, Y, Argov, Z, Sela, I

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P.3.1 GNE myopathy functional activity scale (GNEM-FAS): Development of a disease-specific instrument for measuring function and independence von Skrinar, A.M, Argov, Z, Caraco, Y, Kolodny, E, Lau, H, Pestronk, A, Shieh, P, Bronstein, F, Esposito, A, Feinsod-Meiri, Y, Florence, J, Fowler, E, Greenberg, M, Malkus, E, Rebibo, O, Siener, C, Mayhew, J.E

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P.3.2 Characterization of strength and function in adults with inclusion body myopathy (HIBM)/GNE myopathy von Mayhew, J.E, Skrinar, A.M, Bronstein, F, Esposito, A, Feinsod-Meiri, Y, Florence, J, Fowler, E, Greenberg, M, Malkus, E, Rebibo, O, Siener, C, Caraco, Y, Kolodny, E, Lau, H, Pestronk, A, Shieh, P, Argov, Z

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