Flaw Detection of Cast-Steel Safety Parts in Automotive Application von Dizdar, K C, Sahin, H, Ardicli, M, Dispinar, D

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Flaw Detection of Cast-Steel Safety Parts in Automotive Application von Dizdar, K.C., Sahin, H., Ardicli, M., Dispinar, D.

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The impact of LEP gene polymorphisms located at exon 2 ( LEP - Hin fI) and intron 2 ( LEP-Sau 3AI) on growth and reproductive traits in Saanen goats von Senturk, Nursen, Selvi, Tugce Necla, Demir, Mustafa, Ustuner, Hakan, Samli, Hale, Ardicli, Sena

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348P A national plan of action to raise awareness and improve medical care of Duchenne muscular Dystrophy (AIM-DMD) von Akinci, G., Coskun, A., Koken, O., Ardicli, D., Cinar, E., Okur, T., Ayanoglu, C., Bektas Ontas, H., Ontas, E., Cakir, T., Komur, M., Yuksel, D., Yis, U., Topaloglu, H.

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P440 A new nationwide initiative to explore genetic variants in a large Turkish hereditary neuropathy cohort von Akinci, G., Ozyilmaz, B., Parlar, O., Unalp, A., Polat, I., Baydan, F., Karaoglu, P., Gazeteci, P., Dundar, N Olgac, Ardicli, D., Koken, O Yayici, Aksoy, A., Komurcu, M., Cavusoglu, D., Yis, U., Topaloglu, H.

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Nonsense mutation dystrophinopathy: How mutation-specific treatments changed our clinical practice? von Ardicli, D, Konuskan, B, Haliloglu, G, Alikasifoglu, M, Topaloğlu, H

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Neuroimaging signatures of alpha-dystroglycanopathies (ADG): A pictorial review von Ardicli, D, Gocmen, R, Cirak, S, Karakaya, M, Haliloglu, G, Topaloglu, H

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Solving a puzzle: Incidentally detected high creatine kinase level combined with a family history of cardiomyopathy and sudden unexplained death leading to diagnosis of LMNA mutati... von Genc, H. Maras, Ardicli, D, Haliloglu, G, Talim, B, Alikasifoglu, M, Topaloglu, H

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Evaluation of some environmental and genetic factors (CSN3 and AGPAT6 gene) on milk yield and composition in Saanen goats von Dincel, Deniz, Ardicli, Sena, Samli, Hale, Ogan, M. Mustafa, Balci, Faruk

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G.P.222 - Nonsense mutation dystrophinopathy: How mutation-specific treatments changed our clinical practice? von Ardicli, D., Konuskan, B., Haliloglu, G., Alikasifoglu, M., Topaloğlu, H.

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Utility of a next-generation sequencing (NGS)-based neuromuscular disease gene panel in an investigation of 30 families with early-onset presentation from a tertiary pediatric neur... von Ardicli, D., Nowak, K., Haliloglu, G., Goullee, H., Davis, M., Talim, B., Laing, N., Topaloğlu, H.

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P.331 - Utility of a next-generation sequencing (NGS)-based neuromuscular disease gene panel in an investigation of 30 families with early-onset presentation from a tertiary pediat... von Ardicli, D., Nowak, K., Haliloglu, G., Goullee, H., Davis, M., Talim, B., Laing, N., Topaloğlu, H.

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The profile and natural history of congenital muscular dystrophies von Ardicli, D, Maras Genc, H, Seyhan, K, Kahraman, A, Akcil, M, Talim, B, Haliloglu, G, Tunca Yilmaz, O, Alemdaroglu, I, Topaloglu, H, Karaduman, A

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P.172 - Solving a puzzle: Incidentally detected high creatine kinase level combined with a family history of cardiomyopathy and sudden unexplained death leading to diagnosis of LMN... von Genc, H. Maras, Ardicli, D., Haliloglu, G., Talim, B., Alikasifoglu, M., Topaloglu, H.

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P.252 - Neuroimaging signatures of alpha-dystroglycanopathies (ADG): A pictorial review von Ardicli, D., Gocmen, R., Cirak, S., Karakaya, M., Haliloglu, G., Topaloglu, H.

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P.387A novel in situ hybridisation (ISH) assay mapping the in-frame pseudoexon 11 (pE11) expression in cultured dermal fibroblasts (CDF) and skeletal muscle in patients with severe... von Beck, M., Aguti, S., Ala, P., Richard-Loendt, A., Chambers, D., Scaglioni, D., Ardicli, D., Feng, L., Mein, R., Zhou, H., Sewry, C., Sarkozy, A., Torelli, S., Muntoni, F., Phadke, R.

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CONGENITAL MUSCULAR DYSTROPHIES von Silwal, A., Scoto, M., Ridout, D., Schmidt, A., Laverty, A., Henriques, M., D'Argenzio, L., Main, M., Mein, R., Sarkozy, A., Manzur, A., Al-Ghamdi, F., Genetti, C., Abel, F., Haliloglu, G., Ardicli, D., Topaloğlu, H., Beggs, A., Muntoni, F.

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CONGENITAL MUSCULAR DYSTROPHIES: P.324Clinical characteristics and long-term course of selenoprotein N1 related myopathy in a large multi-centric cohort von Silwal, A., Scoto, M., Ridout, D., Schmidt, A., Laverty, A., Henriques, M., D'Argenzio, L., Main, M., Mein, R., Sarkozy, A., Manzur, A., Al-Ghamdi, F., Genetti, C., Abel, F., Haliloglu, G., Ardicli, D., Topaloğlu, H., Beggs, A., Muntoni, F.

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P.348 - The profile and natural history of congenital muscular dystrophies von Ardicli, D., Maras Genc, H., Seyhan, K., Kahraman, A., Akcil, M., Talim, B., Haliloglu, G., Tunca Yilmaz, O., Alemdaroglu, I., Topaloglu, H., Karaduman, A.

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Ureterovesical junction obstruction causes increment in smooth muscle contractility, and cholinergic and adrenergic activity in distal ureter of rabbits von Yalcin, Sule, Ertunc, Mert, Ardicli, Burak, Kabakus, Ismail M, Tas, Taskin S, Sara, Yildirim, Onur, Rustu, Karnak, Ibrahim

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