G.O.3 von Selcen, D

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237P Advancing the understanding of VAMP1-related congenital myasthenic syndrome: phenotypic insights, favorable response to 3,4-diaminopyridine, and clinical characterization of f... von Natera De Benito, D., Pugliese, A., Polavarapu, K., Guergueltcheva, V., Tournev, I., Todorova, A., Ribeiro, J., Fernández-Mayoralas, D.M., Ortez, C., Martorell, L., Estévez-Arias, B., Matalonga, L., Laurie, S., Jou, C., Lau, J., Thompson, R., Shen, X., Engel, A., Nascimento, A., Lochmuller, H., Selcen, D.

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Myofibrillar myopathy: clinical, morphological and genetic studies in 63 patients von Selcen, Duygu, Ohno, Kinji, Engel, Andrew G.

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Congenital myasthenic syndromes: pathogenesis, diagnosis, and treatment von Engel, A G, Shen, X-M, Selcen, D, Sine, S M

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Myofibrillar myopathies von Selcen, Duygu

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Myofibrillar myopathy caused by novel dominant negative αB-crystallin mutations von Selcen, Duygu, Engel, Andrew G.

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O.21 Congenital Myasthenic Syndrome (CMS), autophagic myopathy, and cognitive dysfunction caused by mutations in DPAGT1 von Selcen, D, Shen, X.M, Li, Y, Wieben, E.D, Engel, A.G

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Myofibrillar myopathies von Selcen, Duygu

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Sporadic late onset nemaline myopathy von CHAHIN, Nizar, SELCEN, Duygu, ENGEL, Andrew G

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Myasthenic syndrome caused by plectinopathy von SELCEN, D, JUEL, V. C, HOBSON-WEBB, L. D, SMITH, E. C, STICKLER, D. E, BITE, A. V, OHNO, K, ENGEL, A. G

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A 49-year-old man with contractures, weakness, and cardiac arrhythmia von KISSEL, J. T, DIMBERG, E. L, EMSLIE-SMITH, A. M, SELCEN, D, KEEGAN, B. M

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Zaspopathy in a large classic late-onset distal myopathy family von Griggs, R., Vihola, A., Hackman, P., Talvinen, K., Haravuori, H., Faulkner, G., Eymard, B., Richard, I., Selcen, D., Engel, A., Carpen, O., Udd, B.

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P5.52 Reducing bodies and myofibrillar myopathy features in FHL1 muscular dystrophy von Selcen, D, Bromberg, M.B, Chin, S.S, Engel, A.G

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INV37 Cytoskeletal myopathies – an overview von Selcen, D

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Recurrent respiratory failure in a patient with nemaline and myofibrillar myopathy features von Braksick, S, Fugate, J, Hocker, S, Engel, A, Selcen, D

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62. Congenital myasthenic syndrome due to defects in rapsyn: A large cohort von Milone, M, Shen, X, Selcen, D, Ohno, K, Brengman, J, Iannaccone, S, Harper, C.M, Engel, A

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C.I.4 Myofibrillar myopathies von Selcen, D, Engel, A

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73P Peripheral neuropathy in myofibrillar myopathies (MFM) and MFM gene-related myopathies von Wannarong, T., Milone, M., Selcen, D., Dyck, P., Liewluck, T.

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G.P.11.11 Myasthenic syndrome due to defects in rapsyn: Clinical and molecular findings in 39 patients von Milone, M, Shen, X.M, Selcen, D, Ohno, K, Brengman, J, Iannaccone, S.T, Harper, C.M, Engel, A.G

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A 12-Year Review of Clinical Practice Patterns in Dupuytren Contracture Based on Continuous Certification by the American Board of Plastic Surgery von Yuksel, Selcen S., Shah, Nikhil D., Sasson, Daniel C., Kearney, Aaron M., Dzwierzynski, William, Gosain, Arun K.

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