참고문헌 (40)

1. Polymeropoulos, Mihael H., Lavedan, Christian, Leroy, Elisabeth, Ide, Susan E., Dehejia, Anindya, Dutra, Amalia, Pike, Brian, Root, Holly, Rubenstein, Jeffrey, Boyer, Rebecca, Stenroos, Edward S., Chandrasekharappa, Settara, Athanassiadou, Aglaia, Papapetropoulos, Theodore, Johnson, William G., Lazzarini, Alice M., Duvoisin, Roger C., Di Iorio, Giuseppe, Golbe, Lawrence I., Nussbaum, Robert L.. Mutation in the α-Synuclein Gene Identified in Families with Parkinson's Disease. Science, vol.276, no.5321, 2045-2047.

   상세보기

2. Krüger, Rejko, Kuhn, Wilfried, Müller, Thomas, Woitalla, Dirk, Graeber, Manuel, Kösel, Sigfried, Przuntek, Horst, Epplen, Jörg T., Schols, Ludger, Riess, Olaf. AlaSOPro mutation in the gene encoding α-synuclein in Parkinson's disease. Nature genetics, vol.18, no.2, 106-108.

   상세보기

3. Gasser, Thomas, Müller-Myhsok, Bertram, Wszolek, Zbigniew K., Oehlmann, Ralph, Calne, Donald B., Bonifati, Vincenzo, Bereznai, Benjamin, Fabrizio, Edito, Vieregge, Peter, Horstmann, Rolf D.. A susceptibility locus for Parkinson's disease maps to chromosome 2p13. Nature genetics, vol.18, no.3, 262-265.

   상세보기

4. Farrer, M, Gwinn-Hardy, K, Muenter, M, DeVrieze, F W, Crook, R, Perez-Tur, J, Lincoln, S, Maraganore, D, Adler, C, Newman, S, MacElwee, K, McCarthy, P, Miller, C, Waters, C, Hardy, J. A chromosome 4p haplotype segregating with Parkinson's disease and postural tremor.. Human molecular genetics, vol.8, no.1, 81-85.

   상세보기

5. Abbas, N, Lücking, C B, Ricard, S, Dürr, A, Bonifati, V, De Michele, G, Bouley, S, Vaughan, J R, Gasser, T, Marconi, R, Broussolle, E, Brefel-Courbon, C, Harhangi, B S, Oostra, B A, Fabrizio, E, Böhme, G A, Pradier, L, Wood, N W, Filla, A, Meco, G, Denefle, P, Agid, Y, Brice, A. A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease.. Human molecular genetics, vol.8, no.4, 567-574.

   상세보기

6. Kitada, Tohru, Asakawa, Shuichi, Hattori, Nobutaka, Matsumine, Hiroto, Yamamura, Yasuhiro, Minoshima, Shinsei, Yokochi, Masayuki, Mizuno, Yoshikuni, Shimizu, Nobuyoshi. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature, vol.392, no.6676, 605-608.

   상세보기

7. Lücking, Christoph B., Dürr, Alexandra, Bonifati, Vincenzo, Vaughan, Jenny, De Michele, Giuseppe, Gasser, Thomas, Harhangi, Biswadjiet S., Meco, Giuseppe, Denèfle, Patrice, Wood, Nicholas W., Agid, Yves, Nicholl, D., Breteler, M.M.B., Oostra, B.A., De Mari, M., Marconi, R., Filla, A., Bonnet, A.-M., Broussolle, E., Pollak, P., Rascol, O., Rosier, M., Arnould, Brice, Alexis. Association between Early-Onset Parkinson's Disease and Mutations in theParkinGene. The New England journal of medicine, vol.342, no.21, 1560-1567.

   상세보기

8. 10.1002/1531-8249(200007)48:1<65::AID-ANA10>3.0.CO;2-L 

   상세보기

9. Neurosci News Wszolek ZK 66 2 1999 The clinical genetics of Parkinsons's disease 

10. Vieregge, P.. Genetic factors in the etiology of idiopathic Parkinson's disease. Journal of neural transmission. Parkinson's disease and dementia section, vol.8, no.1, 1-37.

    상세보기

11. Snow, B. J., Tooyama, I., McGeer, E. G., Yamada, T., Calne, D. B., Takahashi, H., Kimura, H.. Human positron emission tomographic [¹⁸F]Fluorodopa studies correlate with dopamine cell counts and levels. Annals of neurology, vol.34, no.3, 324-330.

    상세보기

12. Brooks, D. J., Ibanez, V., Sawle, G. V., Playford, E. D., Quinn, N., Mathias, C. J., Lees, A. J., Marsden, C. D., Bannister, R., Frackowiak, R. S. J.. Striatal D₂ receptor status in patients with Parkinson's disease, striatonigral degeneration, and progressive supranuclear palsy, measured with ¹¹C‐raclopride and positron emission tomography. Annals of neurology, vol.31, no.2, 184-192.

    상세보기

13. Samii, A., Markopoulou, K., Wszolek, Z.K., Sossi, V., Dobko, T., Mak, E., Calne, D.B., Stoessl, A.J.. PET studies of parkinsonism associated with mutation in the α-synuclein gene. Neurology, vol.53, no.9, 2097-2097.

    상세보기

14. Gibb, W R, Lees, A J. The relevance of the Lewy body to the pathogenesis of idiopathic Parkinson's disease.. Journal of neurology, neurosurgery, and psychiatry, vol.51, no.6, 745-752.

    상세보기

15. Hoehn, Margaret M., Yahr, Melvin D.. Parkinsonism : onset, progression, and mortality. Neurology, vol.17, no.5, 427-427.

    상세보기

16. Sikk, K., Taba, P., Haldre, S., Bergquist, J., Nyholm, D., Zjablov, G., Asser, T., Aquilonius, S.-M.. Irreversible motor impairment in young addicts – ephedrone, manganism or both?. Acta neurologica Scandinavica, vol.115, no.6, 385-389.

    상세보기

17. Wienhard, Klaus, Dahlbom, Magnus, Eriksson, Lars, Michel, Christian, Bruckbauer, Thomas, Pietrzyk, Uwe, Heiss, Wolf-Dieter. The ECAT EXACT HR : Performance of a New High Resolution Positron Scanner. Journal of computer assisted tomography, vol.18, no.1, 110-118.

    상세보기

18. Patlak, Clifford S., Blasberg, Ronald G.. Graphical Evaluation of Blood-to-Brain Transfer Constants from Multiple-Time Uptake Data. Generalizations. Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism, vol.5, no.4, 584-590.

    상세보기

19. Hume, Susan P., Myers, Ralph, Bloomfield, Peter M., Opacka‐Juffry, Jolanta, Cremer, Jill E., Ahier, Randall G., Luthra, Sajinda K., Brooks, David J., Lammertsma, Adriaan A.. Quantitation of Carbon‐11‐labeled raclopride in rat striatum using positron emission tomography. Synapse, vol.12, no.1, 47-54.

    상세보기

20. Lammertsma, A.A., Hume, S.P.. Simplified Reference Tissue Model for PET Receptor Studies. NeuroImage, vol.4, no.3, 153-158.

    상세보기

21. Brooks, D. J., Ibanez, V., Sawle, G. V., Quinn, N., Lees, A. J., Mathias, C. J., Bannister, R., Marsden, C. D., Frackowiak, R. S. J.. Differing patterns of striatal ¹⁸F‐dopa uptake in Parkinson's disease, multiple system atrophy, and progressive supranuclear palsy. Annals of neurology, vol.28, no.4, 547-555.

    상세보기

22. Fearnley, J M, Lees, A J. Ageing and Parkinson's disease: substantia nigra regional selectivity.. Brain : a journal of neurology, vol.114, no.5, 2283-2301.

    상세보기

23. Firnau, G., Sood, S., Chirakal, R., Nahmias, C., Garnett, E. S.. Cerebral Metabolism of 6-[¹⁸F]Fluoro‐l‐3,4‐Dihydroxyphenylalanine in the Primate. Journal of neurochemistry, vol.48, no.4, 1077-1082.

    상세보기

24. Mori, H., Kondo, T., Yokochi, M., Matsumine, H., Nakagawa-Hattori, Y., Miyake, T., Suda, K., Mizuno, Y.. Pathologic and biochemical studies of juvenile parkinsonism linked to chromosome 6q. Neurology, vol.51, no.3, 890-892.

    상세보기

25. Quantitative imaging: neuroreceptors, neurotransmitters, and enzymes Martin WRW 167 1990 

26. Sawle, G. V., Leenders, K. L., Brooks, D. J., Harwood, G., Lees, A. J., Frackowiak, R. S. J., Marsden, C. D.. Dopa‐responsive dystonia: [¹⁸F]dopa positron emission tomography. Annals of neurology, vol.30, no.1, 24-30.

    상세보기

27. Ichinose, Hiroshi, Ohye, Tamae, Takahashi, Ei-ichi, Seki, Naohiko, Hori, Tada-aki, Segawa, Masaya, Nomura, Yoshiko, Endo, Kotaro, Tanaka, Hajime, Tsuji, Shoji, Fujita, Keisuke, Nagatsu, Toshiharu. Hereditary progressive dystonia with marked diurnal fluctuation caused by mutations in the GTP cyclohydrolase I gene. Nature genetics, vol.8, no.3, 236-242.

    상세보기

28. Nygaard, Torbjoern G., Takahashi, Hirohide, Heiman, Gary A., Snow, Barry J., Fahn, Stanley, Calne, Donald B.. Long‐term treatment response and fluorodopa positron emission tomographic scanning of parkinsonism in a family with dopa‐responsive dystonia. Annals of neurology, vol.32, no.5, 603-608.

    상세보기

29. Tassin, J, Dürr, A, Bonnet, A M, Gil, R, Vidailhet, M, Lücking, C B, Goas, J Y, Durif, F, Abada, M, Echenne, B, Motte, J, Lagueny, A, Lacomblez, L, Jedynak, P, Bartholomé, B, Agid, Y, Brice, A. Levodopa-responsive dystonia. GTP cyclohydrolase I or parkin mutations?. Brain : a journal of neurology, vol.123, no.6, 1112-1121.

    상세보기

30. Kishore, A., Nygaard, T. G., de la Fuente-Fernandez, R., Naini, A. B., Schulzer, M., Mak, E., Ruth, T. J., Calne, D. B., Snow, B. J., Stoessl, A. J.. Striatal D2 receptors in symptomatic and asymptomatic carriers of dopa-responsive dystonia measured with [ ¹¹ C]-raclopride and positron-emission tomography. Neurology, vol.50, no.4, 1028-1032.

    상세보기

31. Künig, Gabriella, Leenders, Klaus L., Antonini, Angelo, Vontobel, Peter, Weindl, Adolf, Meinck, Hans M.. D₂ receptor binding in dopa‐responsive dystonia. Annals of neurology, vol.44, no.5, 758-762.

    상세보기

32. Rinne, U. K., Laihinen, A., Rinne, J. O., Naågren, K., Bergman, J., Ruotsalainen, U.. Positron emission tomography demonstrates dopamine D₂ receptor supersensitivity in the striatum of patients with early Parkinson's disease. Movement disorders : official journal of the Movement Disorder Society, vol.5, no.1, 55-59.

    상세보기

33. Antonini, A, Vontobel, P, Psylla, M, Günther, I, Maguire, P R, Missimer, J, Leenders, K L. Complementary positron emission tomographic studies of the striatal dopaminergic system in Parkinson's disease.. Archives of neurology, vol.52, no.12, 1183-1190.

    상세보기

34. Graham, W.C., Sambrook, M.A., Crossman, A.R.. Differential effect of chronic dopaminergic treatment on dopamine D₁ and D₂ receptors in the monkey brain in MPTP-induced parkinsonism. Brain research, vol.602, no.2, 290-303.

    상세보기

35. Boyce, S., Rupniak, N. M. J., Steventon, M. J., Iversen, S. D.. Nigrostriatal Damage is Required for Induction of Dyskinesias by l-DOPA in Squirrel Monkeys :. Clinical neuropharmacology, vol.13, no.5, 448-458.

    상세보기

36. Volkow, Nora D., Wang, Gene‐Jack, Fowler, Joanna S., Logan, Jean, Schlyer, David, Hitzemann, Robert, Lieberman, Jeffrey, Angrist, Burton, Pappas, Naomi, MacGregor, Robert, Burr, Gail, Cooper, Thomas, Wolf, Alfred P.. Imaging endogenous dopamine competition with [¹¹C]raclopride in the human brain. Synapse, vol.16, no.4, 255-262.

    상세보기

37. Drevets, Wayne C., Price, Julie C., Kupfer, David J., Kinahan, Paul E., Lopresti, Brian, Holt, Daniel, Mathis, Chester. PET Measures of Amphetamine-Induced Dopamine Release in Ventral versus Dorsal Striatum. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, vol.21, no.6, 694-709.

    상세보기

38. Holthoff, V. A., Vieregge, P., Kessler, J., Pietrzyk, U., Herholz, K., Bönner, J., Wagner, R., Wienhard, K., Pawlik, G., Heiss, W.‐D.. Discordant twins with Parkinson's disease: Positron emission tomography and early signs of impaired cognitive circuits. Annals of neurology, vol.36, no.2, 176-182.

    상세보기

39. Piccini, P., Morrish, P. K., Turjanski, N., Sawle, G. V., Burn, D. J., Weeks, R. A., Mark, M. H., Maraganore, D. M., Lees, A. J., Brooks, D. J.. Dopaminergic function in familial Parkinson's disease: A clinical and ¹⁸F‐dopa positron emission tomography study. Annals of neurology, vol.41, no.2, 222-229.

    상세보기

40. Neurology Leenders KL A348 52 2 1999 Investigation of the nigrostriatal dopaminergic system in two brothers with autosomal recessive young‐onset parkinsonism