Ausgabe 6/2011
Inhalt (14 Artikel)
C9ORF72, the new gene on the block, causes C9FTD/ALS: new insights provided by neuropathology
Eileen H. Bigio
Molecular pathology and genetic advances in amyotrophic lateral sclerosis: an emerging molecular pathway and the significance of glial pathology
Paul G. Ince, J. Robin Highley, Janine Kirby, Stephen B. Wharton, Hitoshi Takahashi, Michael J. Strong, Pamela J. Shaw
Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72
Melissa E. Murray, Mariely DeJesus-Hernandez, Nicola J. Rutherford, Matt Baker, Ranjan Duara, Neill R. Graff-Radford, Zbigniew K. Wszolek, Tanis J. Ferman, Keith A. Josephs, Kevin B. Boylan, Rosa Rademakers, Dennis W. Dickson
p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS
Safa Al-Sarraj, Andrew King, Claire Troakes, Bradley Smith, Satomi Maekawa, Istvan Bodi, Boris Rogelj, Ammar Al-Chalabi, Tibor Hortobágyi, Christopher E. Shaw
TDP-43 pathological changes in early onset familial and sporadic Alzheimer’s disease, late onset Alzheimer’s disease and Down’s Syndrome: association with age, hippocampal sclerosis and clinical phenotype
Yvonne S. Davidson, Samantha Raby, Penelope G. Foulds, Andrew Robinson, Jennifer C. Thompson, Stephen Sikkink, Imran Yusuf, Hanan Amin, Daniel DuPlessis, Claire Troakes, Safa Al-Sarraj, Carolyn Sloan, Margaret M. Esiri, Vee P. Prasher, David Allsop, David Neary, Stuart M. Pickering-Brown, Julie S. Snowden, David M. A. Mann
Acute and chronically increased immunoreactivity to phosphorylation-independent but not pathological TDP-43 after a single traumatic brain injury in humans
Victoria E. Johnson, William Stewart, John Q. Trojanowski, Douglas H. Smith
A proteomic study identifies different levels of light chain ferritin in corticobasal degeneration and progressive supranuclear palsy
Abdul Shukkur Ebrahim, Jayanarayan Kulathingal, Melissa E. Murray, Monica Casey-Castanedes, Dennis W. Dickson, Shu-Hui Yen, Daniel Sevlever
Simulated brain biopsy for diagnosing neurodegeneration using autopsy-confirmed cases
Sriram Venneti, John L. Robinson, Subhojit Roy, Matthew T. White, Jennifer Baccon, Sharon X. Xie, John Q. Trojanowski
Fas/FasL-mediated apoptosis and inflammation are key features of acute human spinal cord injury: implications for translational, clinical application
Wen Ru Yu, Michael G. Fehlings
Inner ear lesions in congenital cytomegalovirus infection of human fetuses
Natacha Teissier, Anne-Lise Delezoide, Anne-Elisabeth Mas, Suonavy Khung-Savatovsky, Bettina Bessières, Jeannette Nardelli, Christelle Vauloup-Fellous, Olivier Picone, Nadira Houhou, Jean-François Oury, Thierry Van Den Abbeele, Pierre Gressens, Homa Adle-Biassette
An autopsy case of adult-onset hereditary spastic paraplegia type 2 with a novel mutation in exon 7 of the proteolipid protein 1 gene
Satoshi O. Suzuki, Toru Iwaki, Kenji Arakawa, Hirokazu Furuya, Naoki Fujii, Akiko Iwaki
Multinodular leptomeningeal metastases from ETANTR contain both small blue cell and maturing neuropil elements
B. K. Kleinschmidt-DeMasters, Arianne Boylan, Kelley Capocelli, Philip J. Boyer, Nicholas K. Foreman
Embryonal tumor with abundant neuropil and true rosettes (ETANTR) with loss of morphological but retained genetic key features during progression
Adelheid Woehrer, Irene Slavc, Andreas Peyrl, Thomas Czech, Christian Dorfer, Daniela Prayer, Susanne Stary, Berthold Streubel, Marina Ryzhova, Andrey Korshunov, Stefan M. Pfister, Christine Haberler
Activating L265P mutations of the MYD88 gene are common in primary central nervous system lymphoma
Manuel Montesinos-Rongen, Elzbieta Godlewska, Anna Brunn, Otmar D. Wiestler, Reiner Siebert, Martina Deckert