High prevalence of CACNA1A truncations and broader clinical spectrum in episodic ataxia type 2 von DENIER, C, DUCROS, A, GAYOU, A, PERROUTY, B, SOISSON, T, AUTRET, A, WARTER, J. M, VIGHETTO, A, VAN BOGAERT, P, ALAMOWITCH, S, ROULLET, E, TOURNIER-LASSERVE, E, VAHEDI, K, JOUTEL, A, THIERRY, P, RITZ, A, CASTELNOVO, G, DEONNA, T, GERARD, P, DEVOIZE, J. L

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Phenotypic variability of Aprataxin gene mutations von TRANCHANT, C, FLEURY, M, MOREIRA, M. C, KOENIG, M, WARTER, J. M

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Homozygosity mapping of Marinesco-Sjögren syndrome to 5q31 von LAGIER-TOURENNE, C, TRANEBJAERG, L, CHAIGNE, D, GRIBAA, M, DOLLFUS, H, SILVESTRI, G, BETARD, C, WARTER, J. M, KOENIG, M

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Clinical and molecular features of spinocerebellar ataxia type 6 von STEVANIN, G, DÜRR, A, DAVID, G, DIDIERJEAN, O, CANCEL, G, RIVAUD, S, TOURBAH, A, WARTER, J.-M, AGID, Y, BRICE, A

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Homogeneous phenotype of the gypsy limb-girdle MD with the γ-sarcoglycan C283Y mutation von MERLINI, L, KAPLAN, J.-C, KALAYDJIEVA, L, LETURCQ, F, LEVI-GOMES, A, TOUTAIN, A, TOURNEV, I, URTIZBEREA, A, VALLAT, J.-M, VOIT, T, WARTER, J.-M, NAVARRO, C, BAROIS, A, BONNEAU, D, BRASA, J, ECHENNE, B, GALLANO, P, JARRE, L, JEANPIERRE, M

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Unusual Phenotypic Alteration of β Amyloid Precursor Protein (β APP) Maturation by a New Val-715 → Met β APP-770 Mutation Responsible for Probable Early-Onset Alzheimer's Disease... von Ancolio, K., Dumanchin, C., Barelli, H., Warter, J. M., Brice, A., Campion, D., Frébourg, T., Checler, F.

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Factors associated to hypermanganesemia in patients receiving home parenteral nutrition von REIMUND, J.-M., DIETEMANN, J.-L., WARTER, J.-M., BAUMANN, R., DUCLOS, B.

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Novel muscle chloride channel (CLCN1) mutations in myotonia congenita with various modes of inheritance including incomplete dominance and penetrance von PLASSART-SCHIESS, E, GERVAIS, A, EYMARD, B, LAGUENY, A, POUGET, J, WARTER, J. M, FARDEAU, M, JENTSCH, T. J, FONTAINE, B

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Characterization of new polyclonal antibodies specific for 40 and 42 amino acid-long amyloid beta peptides: their use to examine the cell biology of presenilins and the immunohisto... von Barelli, H, Lebeau, A, Vizzavona, J, Delaere, P, Chevallier, N, Drouot, C, Marambaud, P, Ancolio, K, Buxbaum, J D, Khorkova, O, Heroux, J, Sahasrabudhe, S, Martinez, J, Warter, J M, Mohr, M, Checler, F

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Constitutive muscular abnormalities in culture in spinal muscular atrophy von Braun, S., Warter, J.M., Poindron, P., Croizat, B., Lagrange, M.C.

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Is clonidine growth hormone stimulation a good test to differentiate multiple system atrophy from idiopathic Parkinson's disease? von TRANCHANT, C, GUIRAUD-CHAUMEIL, C, ECHANIZ-LAGUNA, A, WARTER, J. M

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Basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease von TRANCHANT, C, GERANTON, L, GUIRAND-CHAUMEIL, C, MOHR, M, WARTER, J. M

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Mapk Activation Via 5-Hydroxytryptamine 1A Receptor is Involved in the Neuroprotective Effects of Xaliproden von Appert-Collin, A., Duong, F.H.T., Degrace, P. Passilly, Warter, J.-M., Poindron, P., Gies, J.-P.

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Effect of the nonpeptide neurotrophic compound SR 57746A on the phenotypic survival of purified mouse motoneurons von Duong, F H T, Warter, J M, Poindron, P, Passilly, P

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Prednisolone enhances myogenesis and dystrophin-related protein in skeletal muscle cell cultures from mdx mouse von Passaquin, A. C., Metzinger, L., Léger, J. J., Warter, J.-M., Poindron, P.

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Muscle could be the therapeutic target in SMA treatment von Guettier-Sigrist, Séverine, Coupin, Gilliane, Braun, Serge, Warter, Jean-Marie, Poindron, Philippe

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A 7-kDa Prion Protein (PrP) Fragment, an Integral Component of the PrP Region Required for Infectivity, Is the Major Amyloid Protein in Gerstmann-Sträussler-Scheinker Disease A117V... von Tagliavini, Fabrizio, Lievens, Patricia M.-J., Tranchant, Christine, Warter, Jean-Marie, Mohr, Michel, Giaccone, Giorgio, Perini, Francesco, Rossi, Giacomina, Salmona, Mario, Piccardo, Pedro, Ghetti, Bernardino, Beavis, Ronald C., Bugiani, Orso, Frangione, Blas, Prelli, Frances

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Neurotrophins increase motoneurons' ability to innervate skeletal muscle fibers in rat spinal cord-human muscle cocultures von Braun, Serge, Croizat, Bernard, Lagrange, Marie-Claude, Warter, Jean-Marie, Poindron, Philippe

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Spontaneous spike and wave discharges in thalamus and cortex in a rat model of genetic petit mal-like seizures von Vergnes, M., Marescaux, C., Depaulis, A., Micheletti, G., Warter, J.M.

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Neurofibrillary tangles in Gerstmann-Sträussler-Scheinker syndrome with the A117V prion gene mutation von Tranchant, C, Sergeant, N, Wattez, A, Mohr, M, Warter, J M, Delacourte, A

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