Voltage-Gated Sodium Channel Expression and Potentiation of Human Breast Cancer Metastasis von FRASER, Scott P, DISS, James K. J, BRACKENBURY, William J, THEODOROU, Dimis, KOYUTURK, Meral, KAYA, Handan, BATTALOGLU, Esra, DE BELLA, Manuela Tamburo, SLADE, Martin J, TOLHURST, Robert, PALMIERI, Carlo, JIE JIANG, CHIONI, Athina-Myrto, LATCHMAN, David S, COOMBES, R. Charles, DJAMGOZ, Mustafa B. A, MYCIELSKA, Maria E, HUIYAN PAN, YAMACI, Rezan F, PANI, Filippo, BIWY, Zuzanna, KRASOWSKA, Monika, GRZYWNA, Zbigniew

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Warfarin maintenance dose associated with genetic polymorphisms of CYP2C9 von Khaleqsefat, E, Khalaj-Kondori, M, Jabbarpour, Bonyadi, Battaloğlu, E

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PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia von Ozes, B., Karagoz, N., Schüle, R., Rebelo, A., Sobrido, M.‐J., Harmuth, F., Synofzik, M., Pascual, S.I.P., Colak, M., Ciftci‐Kavaklioglu, B., Kara, B., Ordóñez‐Ugalde, A., Quintáns, B., Gonzalez, M.A., Soysal, A., Zuchner, S., Battaloglu, E.

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A Novel Missense Mutation in Human TTF-2 (FKHL15) Gene Associated with Congenital Hypothyroidism But Not Athyreosis von Barış, İ., Arısoy, A. E., Smith, A., Agostini, M., Mitchell, C. S., Park, S. M., Halefoğlu, A. M., Zengin, E., Chatterjee, V. K., Battaloğlu, E.

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An autosomal recessive CMT family with a new mutation in the NDRG1 gene von Goksungur, M.T, Okamoto, Y, Pehlivan, D, Akyüz, K, Battaloglu, E, Deymeer, F, Serdaroglu, P, Lupski, J.R, Parman, Y

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High frequency of GJA12/GJC2 mutations in Turkish patients with Pelizaeus-Merzbacher disease von Bilir, B, Yapici, Z, Yalcinkaya, C, Baris, I, Carvalho, CMB, Bartnik, M, Ozes, B, Eraksoy, M, Lupski, JR, Battaloglu, E

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Deletion pattern in the dystrophin gene in Turks and a comparison with Europeans and Indians von ÖNENGÜT, S., KAVASLAR, G. N., BATTALOĞLU, E., SERDAROĞLU, P., DEYMEER, F., ÖZDEMİR, C., CALAFELL, F., TOLUN, A.

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X-linked Charcot-Marie-Tooth disease and multiple sclerosis von Parman, Y, Ciftci, F, Poyraz, M, Halefoglu, A M, Oge, A E, Eraksoy, M, Saruhan-Direskeneli, G, Deymeer, F, Battaloglu, E

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Genetic spectrum of hereditary neuropathies with onset in the first year of life von Baets, Jonathan, Deconinck, Tine, De Vriendt, Els, Zimo, Magdalena, Yperzeele, Laetitia, Van Hoorenbeeck, Kim, Peeters, Kristien, Spiegel, Ronen, Parman, Yesim, Ceulemans, Berten, Van Bogaert, Patrick, Pou-Serradell, Adolf, Bernert, Günther, Dinopoulos, Argirios, Auer-Grumbach, Michaela, Sallinen, Satu-Leena, Fabrizi, Gian Maria, Pauly, Fernand, Van den Bergh, Peter, Bilir, Birdal, Battaloglu, Esra, Madrid, Ricardo E., Kabzi ska, Dagmara, Kochanski, Andrzej, Topaloglu, Haluk, Miller, Geoffrey, Jordanova, Albena, Timmerman, Vincent, De Jonghe, Peter

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G.P.1.10 Clinicopathological and genetic study of CMT2 von Shugaiv, E, Senergin, B, Battaloglu, E, Serdaroglu, P, Deymeer, F, Akalin, M.A, Parman, Y

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Peripheral Nerve Demyelination Caused by a Mutant Rho GTPase Guanine Nucleotide Exchange Factor, Frabin/FGD4 von Stendel, Claudia, Roos, Andreas, Deconinck, Tine, Pereira, Jorge, Castagner, François, Niemann, Axel, Kirschner, Janbernd, Korinthenberg, Rudolf, Ketelsen, Uwe-Peter, Battaloglu, Esra, Parman, Yesim, Nicholson, Garth, Ouvrier, Robert, Seeger, Jürgen, De Jonghe, Peter, Weis, Joachim, Krüttgen, Alexander, Rudnik-Schöneborn, Sabine, Bergmann, Carsten, Suter, Ueli, Zerres, Klaus, Timmerman, Vincent, Relvas, João B., Senderek, Jan

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DNA ANALYSIS IN TURKISH DUCHENNE BECKER MUSCULAR-DYSTROPHY FAMILIES von BATTALOGLU, E, TELATAR, M, DEYMEER, F, SERDAROGLU, P, KUSEYRI, F, OZDEMIR, C, APAK, M, TOLUN, A

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Mutations in a Gene Encoding a Novel SH3/TPR Domain Protein Cause Autosomal Recessive Charcot-Marie-Tooth Type 4C Neuropathy von Senderek, Jan, Bergmann, Carsten, Stendel, Claudia, Kirfel, Jutta, Verpoorten, Nathalie, De Jonghe, Peter, Timmerman, Vincent, Chrast, Roman, Verheijen, Mark H.G., Lemke, Greg, Battaloglu, Esra, Parman, Yesim, Erdem, Sevim, Tan, Ersin, Topaloglu, Haluk, Hahn, Andreas, Müller-Felber, Wolfgang, Rizzuto, Nicolò, Fabrizi, Gian Maria, Stuhrmann, Manfred, Rudnik-Schöneborn, Sabine, Züchner, Stephan, Michael Schröder, J., Buchheim, Eckhard, Straub, Volker, Klepper, Jörg, Huehne, Kathrin, Rautenstrauss, Bernd, Büttner, Reinhard, Nelis, Eva, Zerres, Klaus

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Clinicopathological and genetic study of early-onset demyelinating neuropathy von Parman, Yeşim, Battaloğlu, Esra, Barış, Ibrahim, Bilir, Birdal, Poyraz, Mürüvvet, Bissar-Tadmouri, Nisrine, Williams, Anna, Ammar, Nadia, Nelis, Eva, Timmerman, Vincent, De Jonghe, Peter, Necefov, Ayaz, Deymeer, Feza, Serdaroğlu, Piraye, Brophy, Peter J., Said, G.

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Absence of KIF1B mutation in a large Turkish CMT2A family suggests involvement of a second gene von BISSAR-TADMOURI, N, NELIS, E, BATTALOGLU, E, ZÜCHNER, S, PARMAN, Y, DEYMEER, F, SERDAROGLU, P, DE JONGHE, P, VAN GERWEN, V, TIMMERMAN, V, SCHRÖDER, J. M

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Mutational analysis and genotype/phenotype correlation in Turkish Charcot-Marie-Tooth Type 1 and HNPP patients von Bissar-Tadmouri, N, Parman, Y, Boutrand, L, Deymeer, F, Serdaroglu, P, Vandenberghe, A, Battaloglu, E

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Charcot-Marie-Tooth disease associated with Type 2 diabetes mellitus von Çelik, M., Forta, H., Parman, Y., Bissar-Tadmouri, N., Demirkirkan, K., Battaloglu, E.

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Reply von Deymeer, F., Matur, Z., Poyraz, M., Battaloglu, E., Oflazer‐Serdaroglu, P., Parman, Y.

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Reply von Deymeer, F., Matur, Z., Poyraz, M., Battaloglu, E., Oflazer-Serdaroglu, P., Parman, Y.

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Reply von Deymeer, F., Matur, Z., Poyraz, M., Battaloglu, E., Oflazer‐Serdaroglu, P., Parman, Y.

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