Chromosomen-Screening bei Tourette-Syndrom (pdf) Dissertation ...

Weitere Magazine

Empfehlungen

Info

Chromosomen-Screening bei Tourette-Syndrom Robertson, M. M. and Trimble, M. R. Normal chromosomal findings in Gilles de la Tourette syndrome. Psychiatric Genetics 3. 1993. Sanberg,P.R., Silver,A.A., Shytle,R.D., Philipp,M.K., Cahill,D.W., Fogelson,H.M., and McConville,B.J. (1997). Nicotine for the treatment of Tourette's syndrome. Pharmacol. Ther. 74, 21-25. Seemuller, F., Dehning, S., Grunze, H., and Muller, N. Tourette's symptoms provoked by lamotrigine in a bipolar patient. Am J Psychiatry 163[1]. 2006. Serra-Mestres,J., Ring,H.A., Costa,D.C., Gacinovic,S., Walker,Z., Lees,A.J., Robertson,M.M., and Trimble,M.R. (2004). Dopamine transporter binding in Gilles de la Tourette syndrome: a [123I]FP- CIT/SPECT study. Acta Psychiatr. Scand. 109, 140-146. Seuchter, S. A., Hebebrand, J., Klug, B., Knapp, M., Lehmkuhl, G., Poustka, F., Schmidt, M., Remschmidt, H., and Baur, M. P. Complex segregation analysis of families ascertained through Gilles de la Tourette syndrome. Genet Epidemiol 18[1]. 2000. Shelley,B.P., Robertson,M.M., and Turk,J. (2007). An individual with Gilles de la Tourette syndrome and Smith-Magenis microdeletion syndrome: is chromosome 17p11.2 a candidate region for Tourette syndrome putative susceptibility genes? J. Intellect. Disabil. Res. 51, 620-624. Simonic, I., Gericke, G. S., Ott, J., and Weber, J. L. Identification of genetic markers associated with Gilles de la Tourette syndrome in an Afrikaner population. Am J Hum Genet 63[3]. 1998. Simonic, I., Nyholt, D. R., Gericke, G. S., Gordon, D., Matsumoto, N., Ledbetter, D. H., Ott, J., and Weber, J. L. Further evidence for linkage of Gilles de la Tourette syndrome (GTS) susceptibility loci on chromosomes 2p11, 8q22 and 11q23-24 in South African Afrikaners. Am J Med Genet 105[2]. 2001. 1908. Singer, H. S., Giuliano, J. D., Hansen, B. H., Hallett, J. J., Laurino, J. P., Benson, M., and Kiessling, L. S. Antibodies against human putamen in children with Tourette syndrome. Neurology 50[6]. 1998. Singer,H.S., Reiss,A.L., Brown,J.E., Aylward,E.H., Shih,B., Chee,E., Harris,E.L., Reader,M.J., Chase,G.A., Bryan,R.N., and . (1993). Volumetric MRI changes in basal ganglia of children with Tourette's syndrome. Neurology 43, 950-956. Singh, D. N., Howe, G. L., Jordan, H. W., and Hara, S. Tourette's syndrome in a black woman with associated triple X and 9p mosaicism. J Natl Med Assoc 74[7]. 1982. State, M. W., Greally, J. M., Cuker, A., Bowers, P. N., Henegariu, O., Morgan, T. M., Gunel, M., DiLuna, M., King, R. A., Nelson, C., Donovan, A., Anderson, G. M., Leckman, J. F., Hawkins, T., Pauls, D. L., Lifton, R. P., and Ward, D. C. Epigenetic abnormalities associated with a chromosome 18(q21-q22) inversion and a Gilles de la Tourette syndrome phenotype. Proc Natl Acad Sci U S A 100[8]. 2003. 1915. Sultana, R., Yu, C. E., Yu, J., Munson, J., Chen, D., Hua, W., Estes, A., Cortes, F., de la Barra, F., Yu, D., Haider, S. T., Trask, B. J., Green, E. D., Raskind, W. H., Disteche, C. M., Wijsman, E., Dawson, G., Storm, D. R., Schellenberg, G. D., and Villacres, E. C. Identification of a novel gene on chromosome 7q11.2 interrupted by a translocation breakpoint in a pair of autistic twins. Genomics 80[2]. 2002. Swedo, S. E., Leonard, H. L., Mittleman, B. B., Allen, A. J., Rapoport, J. L., Dow, S. P., Kanter, M. E., Chapman, F., and Zabriskie, J. Identification of children with pediatric autoimmune neuropsychiatric disorders associated with streptococcal infections by a marker associated with rheumatic fever. Am J Psychiatry 154[1]. 1997. Taylor, J. R., Morshed, S. A., Parveen, S., Mercadante, M. T., Scahill, L., Peterson, B. S., King, R. A., Leckman, J. F., and Lombroso, P. J. An animal model of Tourette's syndrome. Am J Psychiatry 159[4]. 2002. 48
Chromosomen-Screening bei Tourette-Syndrom Taylor, L. D., Krizman, D. B., Jankovic, J., Hayani, A., Steuber, P. C., Greenberg, F., Fenwick, R. G., and Caskey, C. T. 9p monosomy in a patient with Gilles de la Tourette's syndrome. Neurology 41[9]. 1991. Tentler,D., Johannesson,T., Johansson,M., Rastam,M., Gillberg,C., Orsmark,C., Carlsson,B., Wahlstrom,J., and Dahl,N. (2003). A candidate region for Asperger syndrome defined by two 17p breakpoints. Eur. J. Hum. Genet. 11, 189-195. Tourette. Étude sur une affection nerveuse caracterisée par de l`incoordination motrice accompagnée d`écholalie et de coprolalie. Arch Neurol 9[19-42]. 1885. Trousseau, A. Des diverses espèces de chorées. Clinique médicale de l`hotel-dieu de Paris t.II[5 e édit.]. 1873. Vandenbergh, D. J., Thompson, M. D., Cook, E. H., Bendahhou, E., Nguyen, T., Krasowski, M. D., Zarrabian, D., Comings, D., Sellers, E. M., Tyndale, R. F., George, S. R., O'Dowd, B. F., and Uhl, G. R. Human dopamine transporter gene: coding region conservation among normal, Tourette's disorder, alcohol dependence and attention-deficit hyperactivity disorder populations. Mol Psychiatry 5[3]. 2000. Verkerk, A. J., Mathews, C. A., Joosse, M., Eussen, B. H., Heutink, P., and Oostra, B. A. CNTNAP2 is disrupted in a family with Gilles de la Tourette syndrome and obsessive compulsive disorder. Genomics 82[1]. 2003. Walkup, J. T., LaBuda, M. C., Singer, H. S., Brown, J., Riddle, M. A., and Hurko, O. Family study and segregation analysis of Tourette syndrome: evidence for a mixed model of inheritance. Am J Hum Genet 59[3]. 1996. Williams,N.M., Norton,N., Williams,H., Ekholm,B., Hamshere,M.L., Lindblom,Y., Chowdari,K.V., Cardno,A.G., Zammit,S., Jones,L.A., Murphy,K.C., Sanders,R.D., McCarthy,G., Gray,M.Y., Jones,G., Holmans,P., Nimgaonkar,V., Adolfson,R., Osby,U., Terenius,L., Sedvall,G., O'Donovan,M.C., and O- wen,M.J. (2003). A systematic genomewide linkage study in 353 sib pairs with schizophrenia. Am. J. Hum. Genet. 73, 1355-1367. 49
Seite 1 und 2: Aus der Klinik und Poliklinik für
Seite 3 und 4: Chromosomen-Screening bei Tourette-
Seite 47: Chromosomen-Screening bei Tourette-

Chromosomen-Screening bei Tourette-Syndrom (pdf) Dissertation ...

Sie wollen auch ein ePaper? Erhöhen Sie die Reichweite Ihrer Titel.

Template löschen?

Als Template speichern?