Microbleed and microinfarct detection in amyloid angiopathy: a high-resolution MRI-histopathology study (English)
- New search for: van Veluw, Susanne J.
- New search for: Charidimou, Andreas
- New search for: van der Kouwe, Andre J.
- New search for: Lauer, Arne
- New search for: Reijmer, Yael D.
- New search for: Costantino, Isabel
- New search for: Gurol, M. Edip
- New search for: Biessels, Geert Jan
- New search for: Frosch, Matthew P.
- New search for: Viswanathan, Anand
- New search for: Greenberg, Steven M.
- New search for: van Veluw, Susanne J.
- New search for: Charidimou, Andreas
- New search for: van der Kouwe, Andre J.
- New search for: Lauer, Arne
- New search for: Reijmer, Yael D.
- New search for: Costantino, Isabel
- New search for: Gurol, M. Edip
- New search for: Biessels, Geert Jan
- New search for: Frosch, Matthew P.
- New search for: Viswanathan, Anand
- New search for: Greenberg, Steven M.
In:
Brain
;
139
, 12
;
3151-
;
2016
- Article (Journal) / Electronic Resource
-
Title:Microbleed and microinfarct detection in amyloid angiopathy: a high-resolution MRI-histopathology study
-
Contributors:van Veluw, Susanne J. ( author ) / Charidimou, Andreas ( author ) / van der Kouwe, Andre J. ( author ) / Lauer, Arne ( author ) / Reijmer, Yael D. ( author ) / Costantino, Isabel ( author ) / Gurol, M. Edip ( author ) / Biessels, Geert Jan ( author ) / Frosch, Matthew P. ( author ) / Viswanathan, Anand ( author )
-
Published in:Brain ; 139, 12 ; 3151-
-
Publisher:
- New search for: Oxford University Press
-
Publication date:2016-12-01
-
ISSN:
-
DOI:
-
Type of media:Article (Journal)
-
Type of material:Electronic Resource
-
Language:English
-
Source:
Table of contents – Volume 139, Issue 12
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 3051
-
EditorialKullmann, Dimitri M. et al. | 2016
- 3052
-
Interleukin-4 induced 1 (IL4I1) promotes central nervous system remyelinationPluchino, Stefano / Peruzzotti-Jametti, Luca et al. | 2016
- 3054
-
Default mode network, connectivity, traumatic brain injury and post-traumatic amnesiaBigler, Erin D. et al. | 2016
- 3057
-
What is the role of TDP-43 in C9orf72-related amyotrophic lateral sclerosis and frontemporal dementia?Scaber, Jakub / Talbot, Kevin et al. | 2016
- 3059
-
Presymptomatic anterior frontal involvement in corticobasal degenerationKobylecki, Christopher / Mann, David M. et al. | 2016
- 3063
-
Brain networks under attack: robustness properties and the impact of lesionsAerts, Hannelore / Fias, Wim / Caeyenberghs, Karen / Marinazzo, Daniele et al. | 2016
- 3084
-
Self-induced intracerebral gamma oscillations in the human cortexCorlier, Juliana / Rimsky-Robert, Daphné / Valderrama, Mario / Lehongre, Katia / Adam, Claude / Clémenceau, Stéphane / Charpier, Stéphane / Bastin, Julien / Kahane, Philippe / Lachaux, Jean-Philippe et al. | 2016
- 3092
-
Prevention of vincristine-induced peripheral neuropathy by genetic deletion of SARM1 in miceGeisler, Stefanie / Doan, Ryan A. / Strickland, Amy / Huang, Xin / Milbrandt, Jeffrey / DiAntonio, Aaron et al. | 2016
- 3109
-
Pathogenic variants in KCTD7 perturb neuronal K+ fluxes and glutamine transportMoen, Marivi Nabong / Fjær, Roar / Hamdani, El Hassan / Laerdahl, Jon K. / Menchini, Robin Johansen / Vigeland, Magnus Dehli / Sheng, Ying / Undlien, Dag Erik / Hassel, Bjørnar / Salih, Mustafa A. et al. | 2016
- 3121
-
IL4I1 augments CNS remyelination and axonal protection by modulating T cell driven inflammationPsachoulia, Konstantina / Chamberlain, Kelly A. / Heo, Dongeun / Davis, Stephanie E. / Paskus, Jeremiah D. / Nanescu, Sonia E. / Dupree, Jeffrey L. / Wynn, Thomas A. / Huang, Jeffrey K. et al. | 2016
- 3137
-
Disconnection between the default mode network and medial temporal lobes in post-traumatic amnesiaDe Simoni, Sara / Grover, Patrick J. / Jenkins, Peter O. / Honeyfield, Lesley / Quest, Rebecca A. / Ross, Ewan / Scott, Gregory / Wilson, Mark H. / Majewska, Paulina / Waldman, Adam D. et al. | 2016
- 3151
-
Microbleed and microinfarct detection in amyloid angiopathy: a high-resolution MRI-histopathology studyvan Veluw, Susanne J. / Charidimou, Andreas / van der Kouwe, Andre J. / Lauer, Arne / Reijmer, Yael D. / Costantino, Isabel / Gurol, M. Edip / Biessels, Geert Jan / Frosch, Matthew P. / Viswanathan, Anand et al. | 2016
- 3163
-
Genome-wide association study in essential tremor identifies three new lociMüller, Stefanie H. / Girard, Simon L. / Hopfner, Franziska / Merner, Nancy D. / Bourassa, Cynthia V. / Lorenz, Delia / Clark, Lorraine N. / Tittmann, Lukas / Soto-Ortolaza, Alexandra I. / Klebe, Stephan et al. | 2016
- 3170
-
Clinicopathological features of adult-onset neuronal intranuclear inclusion diseaseSone, Jun / Mori, Keiko / Inagaki, Tomonori / Katsumata, Ryu / Takagi, Shinnosuke / Yokoi, Satoshi / Araki, Kunihiko / Kato, Toshiyasu / Nakamura, Tomohiko / Koike, Haruki et al. | 2016
- 3187
-
Exosome secretion is a key pathway for clearance of pathological TDP-43Iguchi, Yohei / Eid, Lara / Parent, Martin / Soucy, Geneviève / Bareil, Christine / Riku, Yuichi / Kawai, Kaori / Takagi, Shinnosuke / Yoshida, Mari / Katsuno, Masahisa et al. | 2016
- 3202
-
Timing and significance of pathological features in C9orf72 expansion-associated frontotemporal dementiaVatsavayai, Sarat C. / Yoon, Soo Jin / Gardner, Raquel C. / Gendron, Tania F. / Vargas, Jose Norberto S. / Trujillo, Andrew / Pribadi, Mochtar / Phillips, Joanna J. / Gaus, Stephanie E. / Hixson, John D. et al. | 2016
- 3217
-
A de novo compound targeting {alpha}-synuclein improves deficits in models of Parkinsons diseaseWrasidlo, Wolfgang / Tsigelny, Igor F. / Price, Diana L. / Dutta, Garima / Rockenstein, Edward / Schwarz, Thomas C. / Ledolter, Karin / Bonhaus, Douglas / Paulino, Amy / Eleuteri, Simona et al. | 2016
- 3237
-
Astrogliopathy predominates the earliest stage of corticobasal degeneration pathologyLing, Helen / Kovacs, Gabor G. / Vonsattel, Jean Paul G / Davey, Karen / Mok, Kin Y / Hardy, John / Morris, Huw R. / Warner, Thomas T. / Holton, Janice L. / Revesz, Tamas et al. | 2016
- 3253
-
Whole-brain analysis reveals increased neuroanatomical asymmetries in dementia for hippocampus and amygdalaWachinger, Christian / Salat, David H. / Weiner, Michael / Reuter, Martin / for the Alzheimer’s Disease Neuroimaging Initiative, et al. | 2016
- 3267
-
Neuro-cognitive mechanisms of simultanagnosia in patients with posterior cortical atrophyNeitzel, Julia / Ortner, Marion / Haupt, Marleen / Redel, Petra / Grimmer, Timo / Yakushev, Igor / Drzezga, Alexander / Bublak, Peter / Preul, Christoph / Sorg, Christian et al. | 2016
- 3281
-
Neurophysiological mechanisms of cortical plasticity impairments in schizophrenia and modulation by the NMDA receptor agonist D-serineKantrowitz, Joshua T. / Epstein, Michael L. / Beggel, Odeta / Rohrig, Stephanie / Lehrfeld, Jonathan M. / Revheim, Nadine / Lehrfeld, Nayla P. / Reep, Jacob / Parker, Emily / Silipo, Gail et al. | 2016
- 3296
-
Medial reward and lateral non-reward orbitofrontal cortex circuits change in opposite directions in depressionCheng, Wei / Rolls, Edmund T. / Qiu, Jiang / Liu, Wei / Tang, Yanqing / Huang, Chu-Chung / Wang, XinFa / Zhang, Jie / Lin, Wei / Zheng, Lirong et al. | 2016
- 3310
-
'Perfect mind: on Shakespeare and the brainMcCrum, Robert et al. | 2016
- 3314
-
John Walton, Lord Walton of Detchant: a man of influence and goodwillCompston, Alastair et al. | 2016
- e67
-
Glial mitochondropathy in infantile neuroaxonal dystrophy: pathophysiological and therapeutic implicationsFarrar, Michelle A. / Teoh, Hooi Ling / Brammah, Susan / Roscioli, Tony / Cardamone, Michael et al. | 2016
- e68
-
Reply: Glial mitochondropathy in infantile neuroaxonal dystrophy: pathophysiological and therapeutic implicationsKinghorn, Kerri J. / Castillo-Quan, Jorge Iván / Li, Li / Bhatia, Kailash P. / Abramov, Andrey Y. / Hardy, John / Partridge, Linda et al. | 2016
- e69
-
The next step for imaging the subthalamic nucleusForstmann, Birte U. / Keuken, Max C. / Alkemade, Anneke et al. | 2016
- e70
-
MORC2 mutation causes severe spinal muscular atrophy-phenotype, cerebellar atrophy, and diaphragmatic paralysisSchottmann, Gudrun / Wagner, Christiane / Seifert, Franziska / Stenzel, Werner / Schuelke, Markus et al. | 2016
- e71
-
Erratum| 2016