Fragile X syndrome-From genes to cognition von Schneider, A., Hagerman, R.J., Hessl, D.

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Prevalence of restless legs syndrome and sleep quality in carriers of the fragile X premutation von Summers, S.M., Cogswell, J., Goodrich, J.E., Mu, Y., Nguyen, D.V., Brass, S.D., Hagerman, R.J.

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Germinal mosaicism for a deletion of the FMR1 gene leading to fragile X syndrome von Jiraanont, Poonnada, Hagerman, R.J, Neri, G, Zollino, M, Murdolo, M, Tassone, F

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Altered hypothalamus–pituitary–adrenal gland axis regulation in the expanded CGG-repeat mouse model for fragile X-associated tremor/ataxia syndrome von Brouwer, J.R, Severijnen, E, de Jong, F.H, Hessl, D, Hagerman, R.J, Oostra, B.A, Willemsen, R

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Characterising repetitive behaviours in young boys with fragile X syndrome von Oakes, A., Thurman, A. J., McDuffie, A., Bullard, L. M., Hagerman, R. J., Abbeduto, L.

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FMR1 CGG repeat length predicts motor dysfunction in premutation carriers von LEEHEY, M. A, BERRY-KRAVIS, E, GANE, L, JACQUEMONT, S, TASSONE, F, GRIGSBY, J, HAGERMAN, R. J, HAGERMAN, P. J, GOETZ, C. G, ZHANG, L, HALL, D. A, LI, L, RICE, C. D, LARA, R, COGSWELL, J, REYNOLDS, A

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Fragile-X–Associated Tremor/Ataxia Syndrome (FXTAS) in Females with the FMR1 Premutation von Hagerman, R.J., Leavitt, B.R., Farzin, F., Jacquemont, S., Greco, C.M., Brunberg, J.A., Tassone, F., Hessl, D., Harris, S.W., Zhang, L., Jardini, T., Gane, L.W., Ferranti, J., Ruiz, L., Leehey, M.A., Grigsby, J., Hagerman, P.J.

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Open-Label Allopregnanolone Treatment of Men with Fragile X-Associated Tremor/Ataxia Syndrome von Wang, J. Y., Trivedi, A. M., Carrillo, N. R., Yang, J., Schneider, A., Giulivi, C., Adams, P., Tassone, F., Kim, K., Rivera, S. M., Lubarr, N., Wu, C.-Y., Irwin, R. W., Brinton, R. D., Olichney, J. M., Rogawski, M. A., Hagerman, R. J.

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Psychological symptoms correlate with reduced hippocampal volume in fragile X premutation carriers von Adams, P.E., Adams, J.S., Nguyen, D.V., Hessl, D., Brunberg, J.A., Tassone, F., Zhang, W., Koldewyn, K., Rivera, S.M., Grigsby, J., Zhang, L., DeCarli, C., Hagerman, P.J., Hagerman, R.J.

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A white paper on a neurodevelopmental framework for drug discovery in autism and other neurodevelopmental disorders von Diaz-Caneja, C.M, State, M.W, Hagerman, R.J, Jacquemont, S, Marin, O, Bagni, C, Umbricht, D, Simonoff, E, de Andres-Trelles, F, Kaale, A, Pandina, G, Gomez-Mancilla, B, Wang, P.P, Cusak, J, Siafis, S, Leucht, S, Parellada, M, Loth, E, Charman, T, Buitelaar, J.K, Murphy, D, Arango, C

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Contrast detection in infants with fragile X syndrome von Farzin, F., Whitney, D., Hagerman, R.J., Rivera, S.M.

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A family with two female siblings with compound heterozygous FMR1 premutation alleles von Basuta, K., Lozano, R., Schneider, A., Yrigollen, C.M., Hessl, D., Hagerman, R.J., Tassone, F.

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An fMRI Study of Working Memory Deficits in Premutation Carriers of the Fragile × Mental Retardation 1 Gene With and Without Fragile X-Associated Tremor/Ataxia Syndrome von Hashimoto, R., Backer, K., Hagerman, R.J., Rivera, S.M.

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A cerebellar tremor/ataxia syndrome among fragile X premutation carriers von Hagerman, P.J., Greco, C.M., Hagerman, R.J.

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Clinical involvement and protein expression in individuals with the FMR1 premutation von Tassone, F., Hagerman, R.J., Taylor, A.K., Mills, J.B., Harris, S.W., Gane, L.W., Hagerman, P.J.

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Genetic and clinical characterization of patients with an interstitial duplication 15q11-q13, emphasizing behavioral phenotype and response to treatment von Thomas, J.A., Johnson, J., Peterson Kraai, T.L., Wilson, R., Tartaglia, N., LeRoux, J., Beischel, L., McGavran, L., Hagerman, R.J.

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Effect of fragile X status categories and FMRP deficits on cognitive profiles estimated by robust pedigree analysis von Loesch, D.Z., Huggins, R.M., Bui, Q.M., Taylor, A.K., Pratt, C., Epstein, J., Hagerman, R.J.

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Prevalence of FMR1 Repeat Expansions in Movement Disorders von Hall, D.A., Hagerman, R.J., Hagerman, P.J., Jacquemont, S., Leehey, M.A.

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O-46 von Cronister, A., Abrams, L., Mcconkie-Rosell, A., Gane, L., Finucane, B., Hagerman, R.J.

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O-46: Fragile X cascade testing and genetic counseling guidelines for patients seen in the infertility setting: A center for disease control and prevention, M.I.N.D Institute and N... von Cronister, A., Abrams, L., Mcconkie-Rosell, A., Gane, L., Finucane, B., Hagerman, R.J.

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