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Autor:
Li, Yi-Ju, Oliveira, Sofia A., Xu, Puting, Martin, Eden R., Stenger, Judith E., Scherzer, Clemens R., Hauser, Michael A., Scott, William K., Small, Gary W., Nance, Martha A., Watts, Ray L., Hubble, Jean P., Koller, William C., Pahwa, Rajesh, Stern, Mathew B., Hiner, Bradley C., Jankovic, Joseph, Goetz, Christopher G., Mastaglia, Frank, Middleton, Lefkos T.
Publikováno v:
Human Molecular Genetics; Dec2003, Vol. 12 Issue 24, p3259-3267, 9p
Autor:
Shigeru Koyano, Masatoyo Nishizawa, Masashi Aoki, Ryuji Kaji, Paola Sandroni, Yasuo Nakahara, Eliezer Masliah, Yuishin Izumi, Sid Gilman, Akio Kikuchi, Masaaki Matsushima, Susumu Kusunoki, Hiroyuki Ishiura, Yaeko Ichikawa, Miho Murata, Mizuki Ito, Tatsuhiko Yuasa, Takeo Kato, Takamichi Hattori, Ullrich Wüllner, Mitsunori Yamada, Atsushi Iwata, Kenju Hara, Caroline M. Tanner, Alexis Brice, Laurie J. Ozelius, Yoshiyuki Kuroiwa, Kazuaki Kanai, Walter A. Kukull, Garth A. Nicholson, Alexandra Durr, Kinya Ishikawa, Tomoyoshi Kondo, Jun Mitsui, Hidenao Sasaki, Hidehiro Mizusawa, Akiyoshi Kakita, Kenji Nakashima, Phillip A. Low, Masahiro Horiuchi, Thomas Klockgether, Shoji Tsuji, Jun Goto, Satoshi Kuwabara, Ichiro Yabe, John Q. Trojanowski, Shigeo Murayama, Hidetoshi Date, Alessandro Filla, Mathew B. Stern, Hiroshi Takashima, Tsutomu Yasuda, Tatiana Foroud, Yuji Takahashi, Hitoshi Takahashi, Gen Sobue, Yasushi Osaki, Osamu Onodera, Nobutaka Hattori, Tatsushi Toda, Virginia M.-Y. Lee, Kazuko Hasegawa, Kimihito Arai, Takashi Matsukawa, Hirohisa Watanabe, Yoshio Momose, Mitsutoshi Yamamoto, Kenichi Yasui, Wataru Satake, Budrul Ahsan, Hijiri Ito
Publikováno v:
Annals of Clinical and Translational Neurology 2(4), 417-426 (2015). doi:10.1002/acn3.185
Annals of Clinical and Translational Neurology
Annals of Clinical and Translational Neurology, Wiley, 2015, 2 (4), pp.417-426 ⟨10.1002/acn3.185⟩
Annals of Clinical and Translational Neurology, 2015, 2 (4), pp.417-426 ⟨10.1002/acn3.185⟩
Annals of Clinical and Translational Neurology
Annals of Clinical and Translational Neurology, Wiley, 2015, 2 (4), pp.417-426 ⟨10.1002/acn3.185⟩
Annals of Clinical and Translational Neurology, 2015, 2 (4), pp.417-426 ⟨10.1002/acn3.185⟩
International audience; Objective : Glucocerebrosidase gene (GBA) variants that cause Gaucher disease are associated with Parkinson disease (PD) and dementia with Lewy bodies (DLB). To investigate the role of GBA variants in multiple system atrophy (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e586c67e40726301ea115b0caa95d74b
https://doi.org/10.1002/acn3.185
https://doi.org/10.1002/acn3.185
Autor:
Li YJ; Department of Medicine, Center for Human Genetics, Institute for Genome Science and Policy, Duke University Medical Center, Box 3445, Durham, NC 27710, USA. yiju.li@duke.edu, Oliveira SA, Xu P, Martin ER, Stenger JE, Scherzer CR, Hauser MA, Scott WK, Small GW, Nance MA, Watts RL, Hubble JP, Koller WC, Pahwa R, Stern MB, Hiner BC, Jankovic J, Goetz CG, Mastaglia F, Middleton LT, Roses AD, Saunders AM, Schmechel DE, Gullans SR, Haines JL, Gilbert JR, Vance JM, Pericak-Vance MA, Hulette C, Welsh-Bohmer KA
Publikováno v:
Human molecular genetics [Hum Mol Genet] 2003 Dec 15; Vol. 12 (24), pp. 3259-67. Date of Electronic Publication: 2003 Oct 21.