Glial fibrillary acidic protein immunoglobulin G as biomarker of autoimmune astrocytopathy: Analysis of 102 patients (English)
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In:
Annals of Neurology
;
81
, 2
;
298-309
;
2017
- Article (Journal) / Electronic Resource
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Title:Glial fibrillary acidic protein immunoglobulin G as biomarker of autoimmune astrocytopathy: Analysis of 102 patients
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Contributors:Flanagan, Eoin P. ( author ) / Hinson, Shannon R. ( author ) / Lennon, Vanda A. ( author ) / Fang, Boyan ( author ) / Aksamit, Allen J. ( author ) / Morris, P. Pearse ( author ) / Basal, Eati ( author ) / Honorat, Josephe A. ( author ) / Alfugham, Nora B. ( author ) / Linnoila, Jenny J. ( author )
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Published in:Annals of Neurology ; 81, 2 ; 298-309
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Publisher:
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Publication date:2017-02-01
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Size:12 pages
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Source:
Table of contents – Volume 81, Issue 2
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.
- 167
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Developing a successful global neurology programSiddiqi, Omar K. / Brown, Merritt / Cooper, Christine / Atadzhanov, Masharip / Lakhi, Shabir / Koralnik, Igor J. et al. | 2017
- 171
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Serotonin transporter in Parkinson's disease: A meta‐analysis of positron emission tomography studiesPagano, Gennaro / Niccolini, Flavia / Fusar‐Poli, Paolo / Politis, Marios et al. | 2017
- 181
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The major histocompatibility complex and antibody‐mediated limbic encephalitisStüve, Olaf / Vernino, Steven et al. | 2017
- 183
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Anti‐LGI1 encephalitis is associated with unique HLA subtypesKim, Tae‐Joon / Lee, Soon‐Tae / Moon, Jangsup / Sunwoo, Jun‐Sang / Byun, Jung‐Ick / Lim, Jung‐Ah / Shin, Yong‐Won / Jun, Jin‐Sun / Lee, Han Sang / Lee, Woo‐Jin et al. | 2017
- 193
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Anti‐LGI1 encephalitis is strongly associated with HLA‐DR7 and HLA‐DRB4van Sonderen, Agnes / Roelen, Dave L. / Stoop, Johannes A. / Verdijk, Robert M. / Haasnoot, Geert W. / Thijs, Roland D. / Wirtz, Paul W. / Schreurs, Marco W. J. / Claas, Frans H. J. / Sillevis Smitt, Peter A. E. et al. | 2017
- 199
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Developmental changes in neuromagnetic rhythms and network synchrony in autismVakorin, Vasily A. / Doesburg, Sam M. / Leung, Rachel C. / Vogan, Vanessa M. / Anagnostou, Evdokia / Taylor, Margot J. et al. | 2017
- 212
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Cytokine therapy‐mediated neuroprotection in a Friedreich's ataxia mouse modelKemp, Kevin C. / Cerminara, Nadia / Hares, Kelly / Redondo, Juliana / Cook, Amelia J. / Haynes, Harry R. / Burton, Bronwen R. / Pook, Mark / Apps, Richard / Scolding, Neil J. et al. | 2017
- 227
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Proteomics of rimmed vacuoles define new risk allele in inclusion body myositisGüttsches, Anne‐Katrin / Brady, Stefen / Krause, Kathryn / Maerkens, Alexandra / Uszkoreit, Julian / Eisenacher, Martin / Schreiner, Anja / Galozzi, Sara / Mertens‐Rill, Janine / Tegenthoff, Martin et al. | 2017
- 240
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Tract‐specific atrophy in focal epilepsy: Disease, genetics, or seizures?Vaughan, David N. / Raffelt, David / Curwood, Evan / Tsai, Meng‐Han / Tournier, Jacques‐Donald / Connelly, Alan / Jackson, Graeme D. et al. | 2017
- 251
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Depolarizing γ‐aminobutyric acid contributes to glutamatergic network rewiring in epilepsyKourdougli, Nazim / Pellegrino, Christophe / Renko, Juho‐Matti / Khirug, Stanislav / Chazal, Geneviève / Kukko‐Lukjanov, Tiina‐Kaisa / Lauri, Sari E. / Gaiarsa, Jean‐Luc / Zhou, Liang / Peret, Angélique et al. | 2017
- 266
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Microtubule‐associated protein 1B: Novel paraneoplastic biomarkerGadoth, Avi / Kryzer, Thomas J. / Fryer, Jim / McKeon, Andrew / Lennon, Vanda A. / Pittock, Sean J. et al. | 2017
- 278
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Pseudofeeders on fetal magnetic resonance imaging predict outcome in vein of Galen malformationsSaliou, Guillaume / Vraka, Irène / Teglas, Jean‐Paul / Senat, Marie‐Victoire / Durand, Philippe / Colmant, Claire / Ozanne, Augustin / Martinovic, Jelena / Tissiere, Pierre / Adamsbaum, Catherine et al. | 2017
- 287
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Natural history of pure autonomic failure: A United States prospective cohortKaufmann, Horacio / Norcliffe‐Kaufmann, Lucy / Palma, Jose‐Alberto / Biaggioni, Italo / Low, Phillip A. / Singer, Wolfgang / Goldstein, David S. / Peltier, Amanda C. / Shibao, Cyndia A. / Gibbons, Christopher H. et al. | 2017
- 298
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Glial fibrillary acidic protein immunoglobulin G as biomarker of autoimmune astrocytopathy: Analysis of 102 patientsFlanagan, Eoin P. / Hinson, Shannon R. / Lennon, Vanda A. / Fang, Boyan / Aksamit, Allen J. / Morris, P. Pearse / Basal, Eati / Honorat, Josephe A. / Alfugham, Nora B. / Linnoila, Jenny J. et al. | 2017
- 310
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Eye‐tracking–based assessment suggests preserved well‐being in locked‐in patientsLinse, Katharina / Rüger, Wolfgang / Joos, Markus / Schmitz‐Peiffer, Henning / Storch, Alexander / Hermann, Andreas et al. | 2017
- 316
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Genomic analysis reveals frequent TRAF7 mutations in intraneural perineuriomasKlein, Christopher J. / Wu, Yanhong / Jentoft, Mark E. / Mer, Georges / Spinner, Robert J. / Dyck, P. James B. / Dyck, Peter J. / Mauermann, Michelle L. et al. | 2017
- 322
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Do repetitive Valsalva maneuvers reduce glymphatic clearance?Wostyn, Peter / Van Dam, Debby / Audenaert, Kurt / De Deyn, Peter Paul et al. | 2017
- 322
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ReplyJu, Yo‐El S. / Holtzman, David M. et al. | 2017
- 323
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[11C]PBR‐28 positron emission tomography in multiple sclerosis: Neuroinflammation or otherwise?Raffel, Joel / Sridharan, Sujata / Nicholas, Richard et al. | 2017
- 325
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KCNA2 mutations are rare in hereditary spastic paraplegiaGan‐Or, Ziv / Yoon, Grace / Suchowersky, Oksana / Dupré, Nicolas / Rouleau, Guy A. et al. | 2017
- 326
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De novo KCNA2 mutations cause hereditary spastic paraplegiaManole, Andreea / Männikkö, Roope / Hanna, Michael G. / Kullmann, Dimitri M. / Houlden, Henry / SYNAPS study group et al. | 2017
- 329
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Simvastatin is associated with decreased risk of Parkinson diseaseBrakedal, Brage / Haugarvoll, Kristoffer / Tzoulis, Charalampos et al. | 2017
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Issue Information| 2017
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Annals of Neurology: Volume 81, Number 2, February 2017| 2017