Transmitter concentration profiles in the synaptic cleft: an analytical model of release and diffusion von Kleinle, J., Vogt, K., Lüscher, H.R., Müller, L., Senn, W., Wyler, K., Streit, J.

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Pattern Generation by Two Coupled Time-Discrete Neural Networks with Synaptic Depression von Senn, W., Wannier, Th, Kleinle, J., Lüscher, H.-R., Müller, L., Streit, J., Wyler, K.

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Size principle and information theory von Senn, W, Wyler, K, Clamann, H P, Kleinle, J, Lüscher, H R, Müller, L

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Structural and physiological properties of connections between individual reticulospinal axons and lumbar motoneurons of the frog von Dityatev, Alexander E., Chmykhova, Nadejda M., Dityateva, Galina V., Babalian, Alexander L., Kleinle, Josef, Clamann, H. Peter

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Recruitment by size and principle of least action von Senn, Walter, Wyler, K., Clamann, Hans Peter, Kleinle, J., Larkum, M., Lüscher, H.-R., Müller, L., Streit, J., Vogt, K., Wannier, T.

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Delineating MT-ATP6-associated disease: From isolated neuropathy to early onset neurodegeneration von Stendel, Claudia, Neuhofer, Christiane, Floride, Elisa, Yuqing, Shi, Ganetzky, Rebecca D., Park, Joohyun, Freisinger, Peter, Kornblum, Cornelia, Kleinle, Stephanie, Schöls, Ludger, Distelmaier, Felix, Stettner, Georg M., Büchner, Boriana, Falk, Marni J., Mayr, Johannes A., Synofzik, Matthis, Abicht, Angela, Haack, Tobias B., Prokisch, Holger, Wortmann, Saskia B., Murayama, Kei, Fang, Fang, Klopstock, Thomas

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Delineating MT-ATP6-associated disease. From isolated neuropathy to early onset neurodegeneration von Stendel, Claudia, Neuhofer, Christiane, Floride, Elisa, Yuqing, Shi, Ganetzky, Rebecca D, Park, Joohyun, Freisinger, Peter, Kornblum, Cornelia, Kleinle, Stephanie, Schöls, Ludger, Distelmaier, Felix, Stettner, Georg M, Büchner, Boriana, Falk, Marni J, Mayr, Johannes A, Synofzik, Matthis, Abicht, Angela, Haack, Tobias B, Prokisch, Holger, Wortmann, Saskia B, Murayama, Kei, Fang, Fang, Klopstock, Thomas

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Progressive myoclonus epilepsy and mitochondrial myopathy associated with mutations in the tRNA(Ser(UCN)) gene von Jaksch, M, Klopstock, T, Kurlemann, G, Dörner, M, Hofmann, S, Kleinle, S, Hegemann, S, Weissert, M, Müller-Höcker, J, Pongratz, D, Gerbitz, K D

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Respiratory chain deficiency in nonmitochondrial disease von Pyle, Angela, Nightingale, Helen J, Griffin, Helen, Abicht, Angela, Kirschner, Janbernd, Baric, Ivo, Cuk, Mario, Douroudis, Konstantinos, Feder, Lea, Kratz, Markus, Czermin, Birgit, Kleinle, Stephanie, Santibanez-Koref, Mauro, Karcagi, Veronika, Holinski-Feder, Elke, Chinnery, Patrick F, Horvath, Rita

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A systematic mutation screen of 10 nuclear and 25 mitochondrial candidate genes in 21 patients with cytochrome c oxidase (COX) deficiency shows tRNA(Ser)(UCN) mutations in a subgro... von Jaksch, M, Hofmann, S, Kleinle, S, Liechti-Gallati, S, Pongratz, D E, Müller-Höcker, J, Jedele, K B, Meitinger, T, Gerbitz, K D

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Frequency of mitochondrial transfer RNA mutations and deletions in 225 patients presenting with respiratory chain deficiencies von Jaksch, Michaela, Kleinle, Stephanie, Scharfe, Curt, Klopstock, Thomas, Pongratz, Dieter, Müller-Höcker, Josef, Gerbitz, Klaus-D, Liechti-Gallati, Sabina, Lochmuller, Hanns, Horvath, Rita

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Molekulare Autopsie nach plötzlichem Herztod: Ergänzende Untersuchungen nach unauffälligen Sektionsbefunden von Diebold, I., Pickl, J., Schön, U., Kleinle, S., Laner, A., Benet-Pages, A., Abicht, A., Skopp, G., Musshoff, F., Holinski-Feder, E.

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Detection and characterization of mitochondrial DNA rearrangements in Pearson and Kearns-Sayre syndromes by long PCR von KLEINLE, S, WIESMANN, U, SUPERTI-FURGA, A, KRÄHENBÜHL, S, BOLTSHAUSER, E, REICHEN, J, LIECHTI-GALLATI, S

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Problems in detecting mosaic DNA methylation in Angelman syndrome von HORSTHEMKE, Bernhard, LICH, Christina, JANSSEN, Bart, KLEINLE, Stephanie, KOCHHAN, Lothar, KRASEMANN, Ernst, KRAUS, Cornelia, KROISEL, Peter, PLENDL, Hansjörg, PURMANN, Sabine, SANDER, Gabriele, SKLADNY, Heyko, BUITING, Karin, SPITZER, Eva, THAMM-MÜCKE, Barbara, VARON-MATEEVA, Raymonda, WEINHÄUSEL, Andreas, WEIRICH, Helga, ACHMANN, Roland, AULEHLA-SCHOLZ, Christa, BAUMER, Alessandra, BÜRGER, Joachim, DWORNICZAK, Bernd, GLÄSER, Dieter, HOLINSKI-FEDER, Elke

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Reconstruction and subsurface lattice distortions in the (2 × 1)O-Ni(110) structure: A LEED analysis von Kleinle, G., Wintterlin, J., Ertl, G., Behm, R.J., Jona, F., Moritz, W.

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Structure determination of an adsorbate-induced multilayer reconstruction: (1×2)-H/Ni(110) von KLEINLE, G, PENKA, V, BEHM, R. J, ERTL, G, MORITZ, W

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Delineating MT-ATP6-associated disease von Stendel, Claudia, Neuhofer, Christiane, Floride, Elisa, Shi, Yuqing, Ganetzky, Rebecca D, Park, Joohyun, Freisinger, Peter, Kornblum, Cornelia, Kleinle, Stephanie, Schoels, Ludger, Distelmaier, Felix, Stettner, Georg M, Buechner, Boriana, Falk, Marni J, Mayr, Johannes A, Synofzik, Matthis, Abicht, Angela, Haack, Tobias B, Prokisch, Holger, Wortmann, Saskia B, Murayama, Kei, Fang, Fang, Klopstock, Thomas

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Mechanistic and energetic aspects of the H-induced (1×2) reconstructed structures on Ni(110) and Pd(110) von Kleinle, G., Skottke, M., Penka, V., Ertl, G., Behm, R.J., Moritz, W.

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Progressive myoclonus epilepsy and mitochondrial myopathy associated with mutations in the tRNAser(UCN) gene von Jaksch, Michaela, Klopstock, Thomas, Kurlemann, Gerd, Dörner, Marion, Hofmann, Sabine, Kleinle, Stephanie, Hegemann, Stephan, Weissert, Markus, MüLler-Höcker, Josef, Pongratz, Dieter, Gerbitz, Klus-Dieter

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Respiratory chain deficiency in nonmitochondrial disease von Pyle, Angela, Nightingale, Helen J, Griffin, Helen, Abicht, Angela, Kirschner, Janbernd, Baric, Ivo, Cuk, Mario, Douroudis, Konstantinos, Feder, Lea, Kratz, Markus, Czermin, Birgit, Kleinle, Stephanie, Santibanez-Koref, Mauro, Karcagi, Veronika, Holinski-Feder, Elke, Chinnery, Patrick F, Horvath, Rita

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