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

Results: 13

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
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
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
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
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
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
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
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
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
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

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

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

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

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

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.

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

Kurt Jellinger Prize 2010 for Outstanding Scientific Writing in Neuropathology.

Brain damage in a large cohort of solvent abusers.

Congenital myotonic dystrophy can show congenital fiber type disproportion pathology.

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.