Issue 4/2005
Content (15 Articles)
Constant and severe involvement of Betz cells in corticobasal degeneration is not consistent with pyramidal signs: a clinicopathological study of ten autopsy cases
Kuniaki Tsuchiya, Shigeo Murayama, Kazuko Mitani, Tatsuro Oda, Kunimasa Arima, Masaru Mimura, Hiroshi Nagura, Chie Haga, Haruhiko Akiyama, Hiroshi Yamanouchi, Hidehiro Mizusawa
Humanin detected in skeletal muscles of MELAS patients: a possible new therapeutic agent
Shingo Kariya, Makito Hirano, Yoshiko Furiya, Kazuma Sugie, Satoshi Ueno
Tuft-shaped astrocytes in Lewy body disease
Nozomi Hishikawa, Yoshio Hashizume, Mari Yoshida, Jun-ichi Niwa, Fumiaki Tanaka, Gen Sobue
Secretoglobins in the human pituitary: high expression of lipophilin B and its down-regulation in pituitary adenomas
Anna Sjödin, Dongsheng Guo, Morten Lund-Johansen, Bård Kronen Krossnes, Peer Lilleng, Roger Henriksson, Håkan Hedman
Losses of chromosomes 1p and 19q are rare in pediatric oligodendrogliomas
Portia A. Kreiger, Yoshifumi Okada, Scott Simon, Lucy B. Rorke, David N. Louis, Jeffrey A. Golden
OPA1, associated with autosomal dominant optic atrophy, is widely expressed in the human brain
Stefanie Bette, Holger Schlaszus, Bernd Wissinger, Richard Meyermann, Michel Mittelbronn
Interneuron deficits in patients with the Miller-Dieker syndrome
MacLean Pancoast, William Dobyns, Jeffrey A. Golden
A new murine model of giant proximal axonopathy
D. D. Tshala-Katumbay, V. S. Palmer, R. J. Kayton, M. I. Sabri, P. S. Spencer
The enlarging spectrum of desminopathies: new morphological findings, eastward geographic spread, novel exon 3 desmin mutation
Alexandra Vrabie, Lev G. Goldfarb, Alexey Shatunov, Andrea Nägele, Peter Fritz, Ingo Kaczmarek, Hans H. Goebel
Redistribution of the water channel protein aquaporin-4 and the K+ channel protein Kir4.1 differs in low- and high-grade human brain tumors
Arne Warth, Michel Mittelbronn, Hartwig Wolburg
Extending the clinicopathological spectrum of neurofilament inclusion disease
Keith A. Josephs, Hirotake Uchikado, Rodney D. McComb, Rifaat Bashir, Zbigniew Wszolek, Jerry Swanson, Joseph Matsumoto, Gerry Shaw, Dennis W. Dickson
Congenital disorder of glycosylation type Ia: a clinicopathological report of a newborn infant with cerebellar pathology
E. Aronica, A. A. M. W. van Kempen, M. van der Heide, B. T. Poll-The, H. J. van Slooten, D. Troost, J. M. Rozemuller-Kwakkel
Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene (PRNP) and a 17-kDa prion protein fragment
Sigrun Roeber, Bjarne Krebs, Manuela Neumann, Otto Windl, Inga Zerr, Eva-Maria Grasbon-Frodl, Hans A. Kretzschmar
Fulminant inflammatory leukoencephalopathy associated with HAART-induced immune restoration in AIDS-related progressive multifocal leukoencephalopathy
Aurélie Vendrely, Boris Bienvenu, Jacques Gasnault, Jean Baptiste Thiebault, Dominique Salmon, Françoise Gray