Works matching IS 00016322 AND DT 2010 AND VI 119 AND IP 4

Results: 13

Autopsy study of cerebellar degeneration in siblings with ataxia-telangiectasia-like disorder.

Published in:

2010

By:

Oba, Daiju;
Hayashi, Masaharu;
Minamitani, Motoyuki;
Hamano, Shinichiro;
Uchisaka, Naoki;
Kikuchi, Akira;
Kishimoto, Hiroshi;
Takagi, Masatoshi;
Morio, Tomohiro;
Mizutani, Shuki

Publication type:

Report

The prognostic IDH1 R132 mutation is associated with reduced NADP+-dependent IDH activity in glioblastoma.

Published in:

Acta Neuropathologica, 2010, v. 119, n. 4, p. 487, doi. 10.1007/s00401-010-0645-6

By:

Bleeker, Fonnet E.;
Atai, Nadia A.;
Lamba, Simona;
Jonker, Ard;
Rijkeboer, Denise;
Bosch, Klazien S.;
Tigchelaar, Wikky;
Troost, Dirk;
Vandertop, W. Peter;
Bardelli, Alberto;
Van Noorden, Cornelis J. F.

Publication type:

Article

Novel myosin heavy chain immunohistochemical double staining developed for the routine diagnostic separation of I, IIA and IIX fibers.

Published in:

Acta Neuropathologica, 2010, v. 119, n. 4, p. 495, doi. 10.1007/s00401-010-0643-8

By:

Raheem, Olayinka;
Huovinen, Sanna;
Suominen, Tiina;
Haapasalo, Hannu;
Udd, Bjarne

Publication type:

Article

Differences in aberrant expression and splicing of sarcomeric proteins in the myotonic dystrophies DM1 and DM2.

Published in:

Acta Neuropathologica, 2010, v. 119, n. 4, p. 465, doi. 10.1007/s00401-010-0637-6

By:

Vihola, Anna;
Bachinski, Linda L.;
Sirito, Mario;
Olufemi, Shodimu-Emmanuel;
Hajibashi, Shohrae;
Baggerly, Keith A.;
Raheem, Olayinka;
Haapasalo, Hannu;
Suominen, Tiina;
Holmlund-Hampf, Jeanette;
Paetau, Anders;
Cardani, Rosanna;
Meola, Giovanni;
Kalimo, Hannu;
Edström, Lars;
Krahe, Ralf;
Udd, Bjarne

Publication type:

Article

Rapid and sensitive assessment of the IDH1 and IDH2 mutation status in cerebral gliomas based on DNA pyrosequencing.

Published in:

Acta Neuropathologica, 2010, v. 119, n. 4, p. 501, doi. 10.1007/s00401-010-0647-4

By:

Felsberg, Jörg;
Wolter, Marietta;
Seul, Heike;
Friedensdorf, Britta;
Göppert, Matthias C.;
Sabel, Michael C.;
Reifenberger, Guido

Publication type:

Article

Mutant IDH1-specific immunohistochemistry distinguishes diffuse astrocytoma from astrocytosis.

Published in:

2010

By:

Camelo-Piragua, Sandra;
Jansen, Michael;
Ganguly, Aniruddha;
Kim, J. ChulMin;
Louis, David N.;
Nutt, Catherine L.

Publication type:

Letter

Prevalence of dementia disorders in the oldest-old: an autopsy study.

Published in:

Acta Neuropathologica, 2010, v. 119, n. 4, p. 421, doi. 10.1007/s00401-010-0654-5

By:

Jellinger, Kurt A.;
Attems, Johannes

Publication type:

Article

Protein coding of neurodegenerative dementias: the neuropathological basis of biomarker diagnostics.

Published in:

Acta Neuropathologica, 2010, v. 119, n. 4, p. 389, doi. 10.1007/s00401-010-0658-1

By:

Kovacs, Gabor G.;
Botond, Gergő;
Budka, Herbert

Publication type:

Article

Kurt Jellinger Prize 2010 for Outstanding Scientific Writing in Neuropathology.

Published in:: Acta Neuropathologica, 2010, v. 119, n. 4, p. 521, doi. 10.1007/s00401-010-0670-5
Publication type:: Article

Congenital myotonic dystrophy can show congenital fiber type disproportion pathology.

Published in:

Acta Neuropathologica, 2010, v. 119, n. 4, p. 481, doi. 10.1007/s00401-010-0660-7

By:

Tominaga, Kayo;
Hayashi, Yukiko K.;
Goto, Kanako;
Minami, Narihiro;
Noguchi, Satoru;
Nonaka, Ikuya;
Miki, Tetsuro;
Nishino, Ichizo

Publication type:

Article

Brain damage in a large cohort of solvent abusers.

Published in:

Acta Neuropathologica, 2010, v. 119, n. 4, p. 435, doi. 10.1007/s00401-010-0653-6

By:

Al-Hajri, Zahra;
Del Bigio, Marc R.

Publication type:

Article

Loss of murine TDP-43 disrupts motor function and plays an essential role in embryogenesis.

Published in:

Acta Neuropathologica, 2010, v. 119, n. 4, p. 409, doi. 10.1007/s00401-010-0659-0

By:

Kraemer, Brian C.;
Schuck, Theresa;
Wheeler, Jeanna M.;
Robinson, Linda C.;
Trojanowski, John Q.;
Lee, Virginia M. Y.;
Schellenberg, Gerard D.

Publication type:

Article

The carboxy-terminal fragment of α1A calcium channel preferentially aggregates in the cytoplasm of human spinocerebellar ataxia type 6 Purkinje cells.

Published in:

Acta Neuropathologica, 2010, v. 119, n. 4, p. 447, doi. 10.1007/s00401-009-0630-0

By:

Ishiguro, Taro;
Ishikawa, Kinya;
Takahashi, Makoto;
Obayashi, Masato;
Amino, Takeshi;
Sato, Nozomu;
Sakamoto, Masaki;
Fujigasaki, Hiroto;
Tsuruta, Fuminori;
Dolmetsch, Ricardo;
Arai, Takao;
Sasaki, Hidenao;
Nagashima, Kazuro;
Kato, Takeo;
Yamada, Mitsunori;
Takahashi, Hitoshi;
Hashizume, Yoshio;
Mizusawa, Hidehiro

Publication type:

Article

Works matching IS 00016322 AND DT 2010 AND VI 119 AND IP 4

Autopsy study of cerebellar degeneration in siblings with ataxia-telangiectasia-like disorder.

The prognostic IDH1<sup> R132</sup> mutation is associated with reduced NADP<sup>+</sup>-dependent IDH activity in glioblastoma.

Novel myosin heavy chain immunohistochemical double staining developed for the routine diagnostic separation of I, IIA and IIX fibers.

Differences in aberrant expression and splicing of sarcomeric proteins in the myotonic dystrophies DM1 and DM2.

Rapid and sensitive assessment of the IDH1 and IDH2 mutation status in cerebral gliomas based on DNA pyrosequencing.

Mutant IDH1-specific immunohistochemistry distinguishes diffuse astrocytoma from astrocytosis.

Prevalence of dementia disorders in the oldest-old: an autopsy study.

Protein coding of neurodegenerative dementias: the neuropathological basis of biomarker diagnostics.

Kurt Jellinger Prize 2010 for Outstanding Scientific Writing in Neuropathology.

Congenital myotonic dystrophy can show congenital fiber type disproportion pathology.

Brain damage in a large cohort of solvent abusers.

Loss of murine TDP-43 disrupts motor function and plays an essential role in embryogenesis.

The carboxy-terminal fragment of α<sub>1A</sub> calcium channel preferentially aggregates in the cytoplasm of human spinocerebellar ataxia type 6 Purkinje cells.