G.O.3 von Selcen, D

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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 myopathy: clinical, morphological and genetic studies in 63 patients von Selcen, Duygu, Ohno, Kinji, 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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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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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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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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Coexisting TIA1 and MYH7 distal myopathy von Brand, P, Dyck, P, Liu, J, Berini, S, Selcen, D, Milone, M

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LRP4 myasthenia: Investigation of a second kinship reveals impaired development and maintenance of the neuromuscular junction von Selcen, D, Ohkawara, B, Shen, X, McEvoy, K, Ohno, K, Engel, A

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Myofibrillar myopathies von Selcen, Duygu

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Online social capital: Understanding e-impulse buying in practice von de Kervenoael, Ronan, Aykac, D. Selcen O., Palmer, Mark

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G.O.3: Severe congenital actin related myofibrillar myopathy von Selcen, D.

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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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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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INV37 Cytoskeletal myopathies – an overview von Selcen, D

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Myofibrillar myopathies von Selcen, Duygu

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Mutations in ZASP define a novel form of muscular dystrophy in humans von Selcen, Duygu, Engel, Andrew G.

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Mutations in myotilin cause myofibrillar myopathy von SELCEN, Duygu, ENGEL, Andrew G

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O.23 A novel desmin mutation causes autosomal recessive limb girdle muscular dystrophy without features of myofibrillar myopathy von Cetin, N, Balci-Hayta, B, Gundesli, H, Korkusuz, P, Purali, N, Talim, B, Tan, E, Selcen, D, Erdem-Ozdamar, S, Dincer, P

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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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