Works matching IS 00016322 AND DT 2011 AND VI 122 AND IP 6

Results: 14

Simulated brain biopsy for diagnosing neurodegeneration using autopsy-confirmed cases.

Published in:

Acta Neuropathologica, 2011, v. 122, n. 6, p. 737, doi. 10.1007/s00401-011-0880-5

By:

Venneti, Sriram;
Robinson, John;
Roy, Subhojit;
White, Matthew;
Baccon, Jennifer;
Xie, Sharon;
Trojanowski, John

Publication type:

Article

Activating L265P mutations of the MYD88 gene are common in primary central nervous system lymphoma.

Published in:

2011

By:

Montesinos-Rongen, Manuel;
Godlewska, Elzbieta;
Brunn, Anna;
Wiestler, Otmar;
Siebert, Reiner;
Deckert, Martina

Publication type:

Letter

Embryonal tumor with abundant neuropil and true rosettes (ETANTR) with loss of morphological but retained genetic key features during progression.

Published in:

2011

By:

Woehrer, Adelheid;
Slavc, Irene;
Peyrl, Andreas;
Czech, Thomas;
Dorfer, Christian;
Prayer, Daniela;
Stary, Susanne;
Streubel, Berthold;
Ryzhova, Marina;
Korshunov, Andrey;
Pfister, Stefan;
Haberler, Christine

Publication type:

Letter

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.

Published in:

Acta Neuropathologica, 2011, v. 122, n. 6, p. 691, doi. 10.1007/s00401-011-0911-2

By:

Al-Sarraj, Safa;
King, Andrew;
Troakes, Claire;
Smith, Bradley;
Maekawa, Satomi;
Bodi, Istvan;
Rogelj, Boris;
Al-Chalabi, Ammar;
Hortobágyi, Tibor;
Shaw, Christopher

Publication type:

Article

A proteomic study identifies different levels of light chain ferritin in corticobasal degeneration and progressive supranuclear palsy.

Published in:

Acta Neuropathologica, 2011, v. 122, n. 6, p. 727, doi. 10.1007/s00401-011-0888-x

By:

Ebrahim, Abdul;
Kulathingal, Jayanarayan;
Murray, Melissa;
Casey-Castanedes, Monica;
Dickson, Dennis;
Yen, Shu-Hui;
Sevlever, Daniel

Publication type:

Article

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.

Published in:

Acta Neuropathologica, 2011, v. 122, n. 6, p. 703, doi. 10.1007/s00401-011-0879-y

By:

Davidson, Yvonne;
Raby, Samantha;
Foulds, Penelope;
Robinson, Andrew;
Thompson, Jennifer;
Sikkink, Stephen;
Yusuf, Imran;
Amin, Hanan;
DuPlessis, Daniel;
Troakes, Claire;
Al-Sarraj, Safa;
Sloan, Carolyn;
Esiri, Margaret;
Prasher, Vee;
Allsop, David;
Neary, David;
Pickering-Brown, Stuart;
Snowden, Julie;
Mann, David

Publication type:

Article

Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72.

Published in:

Acta Neuropathologica, 2011, v. 122, n. 6, p. 673, doi. 10.1007/s00401-011-0907-y

By:

Murray, Melissa;
DeJesus-Hernandez, Mariely;
Rutherford, Nicola;
Baker, Matt;
Duara, Ranjan;
Graff-Radford, Neill;
Wszolek, Zbigniew;
Ferman, Tanis;
Josephs, Keith;
Boylan, Kevin;
Rademakers, Rosa;
Dickson, Dennis

Publication type:

Article

C9ORF72, the new gene on the block, causes C9FTD/ALS: new insights provided by neuropathology.

Published in:

2011

By:

Bigio, Eileen

Publication type:

Editorial

Multinodular leptomeningeal metastases from ETANTR contain both small blue cell and maturing neuropil elements.

Published in:

2011

By:

Kleinschmidt-DeMasters, B.;
Boylan, Arianne;
Capocelli, Kelley;
Boyer, Philip;
Foreman, Nicholas

Publication type:

Letter

Inner ear lesions in congenital cytomegalovirus infection of human fetuses.

Published in:

Acta Neuropathologica, 2011, v. 122, n. 6, p. 763, doi. 10.1007/s00401-011-0895-y

By:

Teissier, Natacha;
Delezoide, Anne-Lise;
Mas, Anne-Elisabeth;
Khung-Savatovsky, Suonavy;
Bessières, Bettina;
Nardelli, Jeannette;
Vauloup-Fellous, Christelle;
Picone, Olivier;
Houhou, Nadira;
Oury, Jean-François;
Den Abbeele, Thierry;
Gressens, Pierre;
Adle-Biassette, Homa

Publication type:

Article

Fas/FasL-mediated apoptosis and inflammation are key features of acute human spinal cord injury: implications for translational, clinical application.

Published in:

Acta Neuropathologica, 2011, v. 122, n. 6, p. 747, doi. 10.1007/s00401-011-0882-3

By:

Yu, Wen;
Fehlings, Michael

Publication type:

Article

An autopsy case of adult-onset hereditary spastic paraplegia type 2 with a novel mutation in exon 7 of the proteolipid protein 1 gene.

Published in:

2011

By:

Suzuki, Satoshi;
Iwaki, Toru;
Arakawa, Kenji;
Furuya, Hirokazu;
Fujii, Naoki;
Iwaki, Akiko

Publication type:

Report

Molecular pathology and genetic advances in amyotrophic lateral sclerosis: an emerging molecular pathway and the significance of glial pathology.

Published in:

Acta Neuropathologica, 2011, v. 122, n. 6, p. 657, doi. 10.1007/s00401-011-0913-0

By:

Ince, Paul;
Highley, J.;
Kirby, Janine;
Wharton, Stephen;
Takahashi, Hitoshi;
Strong, Michael;
Shaw, Pamela

Publication type:

Article

Acute and chronically increased immunoreactivity to phosphorylation-independent but not pathological TDP-43 after a single traumatic brain injury in humans.

Published in:

Acta Neuropathologica, 2011, v. 122, n. 6, p. 715, doi. 10.1007/s00401-011-0909-9

By:

Johnson, Victoria;
Stewart, William;
Trojanowski, John;
Smith, Douglas

Publication type:

Article