Constant and severe involvement of Betz cells in corticobasal degeneration is not consistent with pyramidal signs: a clinicopathological study of ten autopsy cases Kuniaki TsuchiyaShigeo MurayamaHidehiro Mizusawa Regular Paper 25 February 2005 Pages: 353 - 366
Humanin detected in skeletal muscles of MELAS patients: a possible new therapeutic agent Shingo KariyaMakito HiranoSatoshi Ueno Regular Paper 10 March 2005 Pages: 367 - 372
Tuft-shaped astrocytes in Lewy body disease Nozomi HishikawaYoshio HashizumeGen Sobue Regular Paper 25 January 2005 Pages: 373 - 380
Secretoglobins in the human pituitary: high expression of lipophilin B and its down-regulation in pituitary adenomas Anna SjödinDongsheng GuoHåkan Hedman Regular Paper 25 January 2005 Pages: 381 - 386
Losses of chromosomes 1p and 19q are rare in pediatric oligodendrogliomas Portia A. KreigerYoshifumi OkadaJeffrey A. Golden Regular Paper 01 March 2005 Pages: 387 - 392
OPA1, associated with autosomal dominant optic atrophy, is widely expressed in the human brain Stefanie BetteHolger SchlaszusMichel Mittelbronn Regular Paper 08 February 2005 Pages: 393 - 399
Interneuron deficits in patients with the Miller-Dieker syndrome MacLean PancoastWilliam DobynsJeffrey A. Golden Regular Paper 01 March 2005 Pages: 400 - 404
A new murine model of giant proximal axonopathy D. D. Tshala-KatumbayV. S. PalmerP. S. Spencer Regular Paper 10 March 2005 Pages: 405 - 410
The enlarging spectrum of desminopathies: new morphological findings, eastward geographic spread, novel exon 3 desmin mutation Alexandra VrabieLev G. GoldfarbHans H. Goebel Regular Paper 10 March 2005 Pages: 411 - 417
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 WarthMichel MittelbronnHartwig Wolburg Regular Paper 19 February 2005 Pages: 418 - 426
Extending the clinicopathological spectrum of neurofilament inclusion disease Keith A. JosephsHirotake UchikadoDennis W. Dickson Case Report 08 March 2005 Pages: 427 - 432
Congenital disorder of glycosylation type Ia: a clinicopathological report of a newborn infant with cerebellar pathology E. AronicaA. A. M. W. van KempenJ. M. Rozemuller-Kwakkel Case Report 16 February 2005 Pages: 433 - 442
Creutzfeldt-Jakob disease in a patient with an R208H mutation of the prion protein gene (PRNP) and a 17-kDa prion protein fragment Sigrun RoeberBjarne KrebsHans A. Kretzschmar Case Report 01 March 2005 Pages: 443 - 448
Fulminant inflammatory leukoencephalopathy associated with HAART-induced immune restoration in AIDS-related progressive multifocal leukoencephalopathy Aurélie VendrelyBoris BienvenuFrançoise Gray Case Report 01 March 2005 Pages: 449 - 455
Kurt Jellinger Prize for Outstanding Scientific Writing in Neuropathology Announcement 03 May 2005 Pages: 456 - 456