Search Results - "Ozes, B."

PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia by 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.

“…PLA2G6‐associated neurodegeneration (PLAN) and hereditary spastic paraplegia (HSP) are 2 groups of heterogeneous neurodegenerative diseases. In this study, we…”
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High frequency of GJA12/GJC2 mutations in Turkish patients with Pelizaeus-Merzbacher disease by Bilir, B, Yapici, Z, Yalcinkaya, C, Baris, I, Carvalho, CMB, Bartnik, M, Ozes, B, Eraksoy, M, Lupski, JR, Battaloglu, E

“…Bilir B, Yapici Z, Yalcinkaya C, Baris I, Carvalho CMB, Bartnik M, Ozes B, Eraksoy M, Lupski JR, Battaloglu E. High frequency of GJA12/GJC2 mutations in…”
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MUSCLE FUNCTION & HOMEOSTASIS / MOLECULAR THERAPEUTIC APPROACHES: P.63 AAV.CAPN3 gene therapy for Limb-girdle muscular dystrophy type 2A (LGMD2A): Phenotypic improvements in the calpain3 (CAPN3)-null mouse by Ozes, B., Murrey, D., Myers, M., Chen, L., Moss, K., Ridgley, A., Wier, C., Sahenk, Z.

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MUSCLE FUNCTION & HOMEOSTASIS / MOLECULAR THERAPEUTIC APPROACHES by Ozes, B., Murrey, D., Myers, M., Chen, L., Moss, K., Ridgley, A., Wier, C., Sahenk, Z.

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P56 Preliminary study of anti-AAVrh74 seroprevalence following gene transfer by D'Ambrosio, E., Tong, L., Ozes Ak, B., Lehman, K., Sahenk, Z., Mendell, J.

“…The increasing number of gene therapy studies and exclusion of candidates from clinical trials highlights the potential importance of pre-existing antibodies…”
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