Epilepsy and the natural history of Rett syndrome von GLAZE, D. G, PERCY, A. K, MCNAIR, L, LEE, H.-S, SKINNER, S, MOTIL, K. J, NEUL, J. L, BARRISH, J. O, LANE, J. B, GEERTS, S. P, ANNESE, F, GRAHAM, J

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Microbial community changes in a female rat model of Rett syndrome von Gallucci, A., Patterson, K.C., Weit, A.R., Van Der Pol, W.J., Dubois, L.G., Percy, A.K., Morrow, C.D., Campbell, S.L., Olsen, M.L.

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Clinical severity and quality of life in children and adolescents with Rett syndrome von LANE, J. B, LEE, H.-S, ANNESE, F, MCNAIR, L, GRAHAM, J, KHWAJA, O, BARNES, K, KRISCHER, J. P, SMITH, L. W, CHENG, P, PERCY, A. K, GLAZE, D. G, NEUL, J. L, MOTIL, K. J, BARRISH, J. O, SKINNER, S. A

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Early progressive encephalopathy in boys and MECP2 mutations von KANKIRAWATANA, P, LEONARD, H, FABIAN, V, DAVIS, M, JACKSON, J, CHRISTODOULOU, J, KAUFMANN, W. E, RAVINE, D, PERCY, A. K, ELLAWAY, C, SCURLOCK, J, MANSOUR, A, MAKRIS, C. M, DURE, L. S, FRIEZ, M, LANE, J, KIRALY-BORRI, C

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FXYD1, a Modulator of Na+,K+-ATPase Activity, Facilitates Female Sexual Development by Maintaining Gonadotrophin-Releasing Hormone Neuronal Excitability von Garcia-Rudaz, C., Deng, V., Matagne, V., Ronnekleiv, O. K., Bosch, M., Han, V., Percy, A. K., Ojeda, S. R.

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Progressive hearing loss in infants with asymptomatic congenital cytomegalovirus infection von WILLIAMSON, W. D, DEMMLER, G. J, PERCY, A. K, CATLIN, F. I

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Clinical and genetic heterogeneity in benign hereditary chorea von BREEDVELD, G. J, PERCY, A. K, MACDONALD, M. E, DE VRIES, B. B. A, YAPIJAKIS, C, DURE, L. S, IPPEL, E. F, SANDKUIJL, L. A, HEUTINK, P, ARTS, W. F. M

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Mutations in exon 1 of MECP2 are a rare cause of Rett syndrome von Amir, R E, Fang, P, Yu, Z, Glaze, D G, Percy, A K, Zoghbi, H Y, Roa, B B, Van den Veyver, I B

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P.045 Trofinetide for the treatment of Rett syndrome: long-term safety and efficacy results from the open-label LILAC and LILAC-2 studies von Percy, AK, Neul, JL, Benke, TA, Berry-Kravis, EM, Glaze, DG, Marsh, ED, Lamontagne, A, An, D, Bishop, KM, Youakim, JM

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Enlarged parietal foramina : Association with cerebral venous and cortical anomalies von REDDY, A. T, HEDLUND, G. L, PERCY, A. K

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Occipital horn syndrome and a mild Menkes phenotype associated with splice site mutations at the MNK locus von Kaler, Stephen G, Gallo, Linda K, Proud, Virginia K, Percy, Alan K, Mark, Yvonne, Segal, Neil A, Goldstein, David S, Holmes, Courtney S, Gahl, William A

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Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes von Amir, Ruthie E., Van Den Veyver, Ignatia B., Schultz, Rebecca, Malicki, Denise M., Tran, Charles Q., Dahle, E. J., Philippi, Anne, Timar, László, Percy, Alan K., Motil, Kathleen J., Lichtarge, Olivier, O'Brian Smith, E., Glaze, Daniel G., Zoghbi, Huda Y.

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Epidemiology of Rett syndrome : a population-based registry von KOZINETZ, C. A, SKENDER, M. L, MACNAUGHTON, N, ALMES, M. J, SCHULTZ, R. J, PERCY, A. K, GLAZE, D. G

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Electrocardiographic findings in Rett syndrome: An explanation for sudden death? von Sekul, Elizabeth A., Moak, Jeffrey P., Schultz, Rebecca J., Glaze, Daniel G., Dunn, J.Kay, Percy, Alan K.

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Neuropathology of Rett syndrome von JELLINGER, K, ARMSTRONG, D, ZOGHBI, H. Y, PERCY, A. K

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Decreased cerebrospinal fluid levels of β-phenylethylamine in patients with Rett syndrome von Satoi, Mika, Matsuishi, Toyojiro, Yamada, Shigeto, Yamashita, Yushiro, Ohtaki, Etsuo, Mori, Kenji, Riikonen, Raili, Kato, Hirohisa, Percy, Alan K.

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Decreased cerebrospinal fluid levels of substance P in patients with Rett syndrome von Matsuishi, Toyojiro, Nagamitsu, Shinichiro, Yamashita, Yushiro, Murakami, Yoshihiko, Kato, Hirohisa, Kimura, Akihiko, Sakai, Tetsuo, Kimura, Akihiko, Percy, Alan K., Shoji, Hiroshi

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Eliminating institutional child abuse : A road too well traveled von PERCY, A. K

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Rett syndrome: Controlled study of an oral opiate antagonist, naltrexone von Percy, Alan K., Glaze, Daniel G., Schultz, Rebecca J., Zoghbi, Huda Y., Williamson, Daniel, Frost Jr, James D., Jankovic, Joseph J., del Junco, Deborah, Skender, Martha, Waring, Steve, Myer, Edwin C.

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Neurobiology and neurochemistry of Rett syndrome von Percy, A K

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