A Drosophila Genetic Resource of Mutants to Study Mechanisms Underlying Human Genetic Diseases von Yamamoto, Shinya, Jaiswal, Manish, Charng, Wu-Lin, Gambin, Tomasz, Karaca, Ender, Mirzaa, Ghayda, Wiszniewski, Wojciech, Sandoval, Hector, Haelterman, Nele A., Xiong, Bo, Zhang, Ke, Bayat, Vafa, David, Gabriela, Li, Tongchao, Chen, Kuchuan, Gala, Upasana, Harel, Tamar, Pehlivan, Davut, Penney, Samantha, Vissers, Lisenka E.L.M., de Ligt, Joep, Jhangiani, Shalini N., Xie, Yajing, Tsang, Stephen H., Parman, Yesim, Sivaci, Merve, Battaloglu, Esra, Muzny, Donna, Wan, Ying-Wooi, Liu, Zhandong, Lin-Moore, Alexander T., Clark, Robin D., Curry, Cynthia J., Link, Nichole, Schulze, Karen L., Boerwinkle, Eric, Dobyns, William B., Allikmets, Rando, Gibbs, Richard A., Chen, Rui, Lupski, James R., Wangler, Michael F., Bellen, Hugo J.

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Clinical and Genetic Survey for Charcot-Marie-Tooth Neuropathy Based on the Findings in Turkey, a Country with a High Rate of Consanguineous Marriages von Candayan, Ayşe, Parman, Yeşim, Battaloğlu, Esra

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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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MCM3AP in recessive Charcot-Marie-Tooth neuropathy and mild intellectual disability von Ylikallio, Emil, Woldegebriel, Rosa, Tumiati, Manuela, Isohanni, Pirjo, Ryan, Monique M, Stark, Zornitza, Walsh, Maie, Sawyer, Sarah L, Bell, Katrina M, Oshlack, Alicia, Lockhart, Paul J, Shcherbii, Mariia, Estrada-Cuzcano, Alejandro, Atkinson, Derek, Hartley, Taila, Tetreault, Martine, Cuppen, Inge, van der Pol, W Ludo, Candayan, Ayse, Battaloglu, Esra, Parman, Yesim, van Gassen, Koen L I, van den Boogaard, Marie-José H, Boycott, Kym M, Kauppi, Liisa, Jordanova, Albena, Lönnqvist, Tuula, Tyynismaa, Henna

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The first biallelic missense mutation in the FXN gene in a consanguineous Turkish family with Charcot-Marie-Tooth-like phenotype von Candayan, Ayşe, Yunisova, Gulshan, Çakar, Arman, Durmuş, Hacer, Başak, A. Nazlı, Parman, Yeşim, Battaloğlu, Esra

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Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (canvas): an important cause of late-onset ataxia with unique clinical features von Çakar, Arman, Şahin, Erdi, Tezel, Seden, Candayan, Ayşe, Samancı, Bedia, Battaloğlu, Esra, Başak, A. Nazlı, Bilgiç, Başar, Hanağası, Haşmet, Durmuş, Hacer, Parman, Yeşim

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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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Genetic Survey of Autosomal Recessive Peripheral Neuropathy Cases Unravels High Genetic Heterogeneity in a Turkish Cohort von Candayan, Ayşe, Çakar, Arman, Yunisova, Gulshan, Özdağ Acarlı, Ayşe Nur, Atkinson, Derek, Topaloğlu, Pınar, Durmuş, Hacer, Yapıcı, Zuhal, Jordanova, Albena, Parman, Yeşim, Battaloğlu, Esra

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Low dose vincristine-induced severe polyneuropathy in a Hodgkin lymphoma patient: a case report (vincristine-induced severe polyneuropathy) von Cil, Timucin, Altintas, Abdullah, Tamam, Yusuf, Battaloğlu, Esra, Isikdogan, Abdurrahman

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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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Clinical and genetic aspects of hereditary spastic paraplegia in patients from Turkey von Akcakaya, Nihan H., Ak, Burcak Ozes, Gonzalez, Michael A., Zuchner, Stefan, Battaloglu, Esra, Parman, Yesim

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Selective Bilateral Vestibular Neuropathy in a Turkish CMT1B Family With a Novel MPZ Mutation von Akdal, Gülden, Koçoğlu, Koray, Bora, Elçin, Koç, Altuğ, Ülgenalp, Ayfer, Bedir, Mithat, Ala, Rahmi Tümay, Battaloğlu, Esra, Kırkım, Günay, Şengün, İhsan Şükrü, Halmágyi, Gábor Michael

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Motor protein mutations cause a new form of hereditary spastic paraplegia von Caballero Oteyza, Andrés, Battaloğlu, Esra, Ocek, Levent, Lindig, Tobias, Reichbauer, Jennifer, Rebelo, Adriana P, Gonzalez, Michael A, Zorlu, Yasar, Ozes, Burcak, Timmann, Dagmar, Bender, Benjamin, Woehlke, Günther, Züchner, Stephan, Schöls, Ludger, Schüle, Rebecca

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Single Center Experience of SORD Neuropathy in Turkey (P1-1.Virtual) von Çakar, Arman, Candayan, Ayse, Durmus, Hacer, Battaloglu, Esra, Parman, Yesim

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Nerve conduction studies in Charcot-Marie-Tooth disease in a cohort from Turkey von Deymeer, Feza, Matur, Zeliha, Poyraz, Muruvvet, Battaloglu, Esra, Oflazer-Serdaroglu, Piraye, Parman, Yesim

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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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Hereditary neuropathy with liability to pressure palsy (HNPP) in childhood: A case study emphasizing the relevance of detailed electrophysiological examination for suspected HNPP i... von Bayrak, Ayşe Oytun, Battaloglu, Esra, Turker, Hande, Baris, Ibrahim, Oztas, Gurkan

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Distinct Genetic Distribution of Distal Hereditary Motor Neuropathy in Turkey: A Single Centre Experience (P2-11.009) von Cakar, Arman, Candayan, Ayse, Maroofian, Reza, Durmus, Hacer, Houlden, Henry, Battaloglu, Esra, Parman, Fatma Yesim

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Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia von Zimoń, Magdalena, Baets, Jonathan, Almeida-Souza, Leonardo, De Vriendt, Els, Nikodinovic, Jelena, Parman, Yesim, Battaloǧlu, Esra, Matur, Zeliha, Guergueltcheva, Velina, Tournev, Ivailo, Auer-Grumbach, Michaela, De Rijk, Peter, Petersen, Britt-Sabina, Müller, Thomas, Fransen, Erik, Van Damme, Philip, Löscher, Wolfgang N, Barišić, Nina, Mitrovic, Zoran, Previtali, Stefano C, Topaloǧlu, Haluk, Bernert, Günther, Beleza-Meireles, Ana, Todorovic, Slobodanka, Savic-Pavicevic, Dusanka, Ishpekova, Boryana, Lechner, Silvia, Peeters, Kristien, Ooms, Tinne, Hahn, Angelika F, Züchner, Stephan, Timmerman, Vincent, Van Dijck, Patrick, Rasic, Vedrana Milic, Janecke, Andreas R, De Jonghe, Peter, Jordanova, Albena

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Genotypic And Phenotypic Features of Patients with GJB1 Mutations: Single Center Experience (P11-8.003) von Parman, Fatma Yesim, Cakar, Arman, Candayan, Ayse, Durmus, Hacer, Battaloglu, Esra

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