Works matching IS 00016322 AND DT 2005 AND VI 109 AND IP 4

Results: 15

Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene ( PRNP) and a 17-kDa prion protein fragment.

Published in:

Acta Neuropathologica, 2005, v. 109, n. 4, p. 443, doi. 10.1007/s00401-004-0978-0

By:

Roeber, Sigrun;
Krebs, Bjarne;
Neumann, Manuela;
Windl, Otto;
Zerr, Inga;
Grasbon-Frodl, Eva-Maria;
Kretzschmar, Hans A.

Publication type:

Article

Fulminant inflammatory leukoencephalopathy associated with HAART-induced immune restoration in AIDS-related progressive multifocal leukoencephalopathy.

Published in:

Acta Neuropathologica, 2005, v. 109, n. 4, p. 449, doi. 10.1007/s00401-005-0983-y

By:

Vendrely, Aurélie;
Bienvenu, Boris;
Gasnault, Jacques;
Thiebault, Jean Baptiste;
Salmon, Dominique;
Gray, Françoise

Publication type:

Article

Extending the clinicopathological spectrum of neurofilament inclusion disease.

Published in:

Acta Neuropathologica, 2005, v. 109, n. 4, p. 427, doi. 10.1007/s00401-004-0974-4

By:

Josephs, Keith A.;
Uchikado, Hirotake;
McComb, Rodney D.;
Bashir, Rifaat;
Wszolek, Zbigniew;
Swanson, Jerry;
Matsumoto, Joseph;
Shaw, Gerry;
Dickson, Dennis W.

Publication type:

Article

The enlarging spectrum of desminopathies: new morphological findings, eastward geographic spread, novel exon 3 desmin mutation.

Published in:

Acta Neuropathologica, 2005, v. 109, n. 4, p. 411, doi. 10.1007/s00401-005-0980-1

By:

Vrabie, Alexandra;
Goldfarb, Lev G.;
Shatunov, Alexey;
Nägele, Andrea;
Fritz, Peter;
Kaczmarek, Ingo;
Goebel, Hans H.

Publication type:

Article

Tuft-shaped astrocytes in Lewy body disease.

Published in:

Acta Neuropathologica, 2005, v. 109, n. 4, p. 373, doi. 10.1007/s00401-004-0967-3

By:

Hishikawa, Nozomi;
Hashizume, Yoshio;
Yoshida, Mari;
Niwa, Jun-ichi;
Tanaka, Fumiaki;
Sobue, Gen

Publication type:

Article

Secretoglobins in the human pituitary: high expression of lipophilin B and its down-regulation in pituitary adenomas.

Published in:

Acta Neuropathologica, 2005, v. 109, n. 4, p. 381, doi. 10.1007/s00401-004-0972-6

By:

Sjödin, Anna;
Guo, Dongsheng;
Lund-Johansen, Morten;
Krossnes, Bård Kronen;
Lilleng, Peer;
Henriksson, Roger;
Hedman, Håkan

Publication type:

Article

OPA1, associated with autosomal dominant optic atrophy, is widely expressed in the human brain.

Published in:

Acta Neuropathologica, 2005, v. 109, n. 4, p. 393, doi. 10.1007/s00401-004-0970-8

By:

Bette, Stefanie;
Schlaszus, Holger;
Wissinger, Bernd;
Meyermann, Richard;
Mittelbronn, Michel

Publication type:

Article

Congenital disorder of glycosylation type Ia: a clinicopathological report of a newborn infant with cerebellar pathology.

Published in:

Acta Neuropathologica, 2005, v. 109, n. 4, p. 433, doi. 10.1007/s00401-004-0975-3

By:

Aronica, E.;
Kempen, A. A. M. W.;
Heide, M. van der;
Poll-The, B. T.;
Slooten, H. J.;
Troost, D.;
Rozemuller-Kwakkel, J. M.

Publication type:

Article

Redistribution of the water channel protein aquaporin-4 and the K<sup>+</sup> channel protein Kir4.1 differs in low- and high-grade human brain tumors.

Published in:

Acta Neuropathologica, 2005, v. 109, n. 4, p. 418, doi. 10.1007/s00401-005-0984-x

By:

Warth, Arne;
Mittelbronn, Michel;
Wolburg, Hartwig

Publication type:

Article

Constant and severe involvement of Betz cells in corticobasal degeneration is not consistent with pyramidal signs: a clinicopathological study of ten autopsy cases.

Published in:

Acta Neuropathologica, 2005, v. 109, n. 4, p. 353, doi. 10.1007/s00401-004-0966-4

By:

Tsuchiya, Kuniaki;
Murayama, Shigeo;
Mitani, Kazuko;
Oda, Tatsuro;
Arima, Kunimasa;
Mimura, Masaru;
Nagura, Hiroshi;
Haga, Chie;
Akiyama, Haruhiko;
Yamanouchi, Hiroshi;
Mizusawa, Hidehiro

Publication type:

Article

Losses of chromosomes 1p and 19q are rare in pediatric oligodendrogliomas.

Published in:

Acta Neuropathologica, 2005, v. 109, n. 4, p. 387, doi. 10.1007/s00401-004-0976-2

By:

Kreiger, Portia;
Okada, Yoshifumi;
Simon, Scott;
Rorke, Lucy;
Louis, David;
Golden, Jeffrey

Publication type:

Article

Interneuron deficits in patients with the Miller-Dieker syndrome.

Published in:

Acta Neuropathologica, 2005, v. 109, n. 4, p. 400, doi. 10.1007/s00401-004-0979-z

By:

Pancoast, MacLean;
Dobyns, William;
Golden, Jeffrey

Publication type:

Article

A new murine model of giant proximal axonopathy.

Published in:

Acta Neuropathologica, 2005, v. 109, n. 4, p. 405, doi. 10.1007/s00401-005-0982-z

By:

Tshala-Katumbay, D. D.;
Palmer, V. S.;
Kayton, R. J.;
Sabri, M. I.;
Spencer, P. S.

Publication type:

Article

Humanin detected in skeletal muscles of MELAS patients: a possible new therapeutic agent.

Published in:

Acta Neuropathologica, 2005, v. 109, n. 4, p. 367, doi. 10.1007/s00401-004-0965-5

By:

Kariya, Shingo;
Hirano, Makito;
Furiya, Yoshiko;
Sugie, Kazuma;
Ueno, Satoshi

Publication type:

Article

Kurt Jellinger Prize for Outstanding Scientific Writing in Neuropathology.

Published in:: Acta Neuropathologica, 2005, v. 109, n. 4, p. 456, doi. 10.1007/s00401-005-1023-7
Publication type:: Article