Globular Glial Tauopathy Type I Presenting as Atypical Progressive Aphasia, With Comorbid Limbic-Predominant Age-Related TDP-43 Encephalopathy by Robert Rusina, Robert Rusina, Zsolt Csefalvay, Gabor G. Kovacs, Gabor G. Kovacs, Gabor G. Kovacs, Jiri Keller, Jiri Keller, Alena Javurkova, Alena Javurkova, Radoslav Matej, Radoslav Matej

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Adult mitochondrial DNA depletion syndrome with mild manifestations by Josef Finsterer, Gabor G. Kovacs, Uwe Ahting

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Asymptomatic hyper-creatine-kinase-emia as sole manifestation of inclusion body myositis by Josef Finsterer, Claudia Stöllberger, Gabor G. Kovacs

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Cellular iron deposition patterns predict clinical subtypes of multiple system atrophy by Seojin Lee, Ivan Martinez-Valbuena, Anthony E. Lang, Gabor G. Kovacs

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Amyloid-β pathology and cerebral amyloid angiopathy are frequent in iatrogenic Creutzfeldt-Jakob disease after dural grafting by Karl Frontzek, Mirjam I. Lutz, Adriano Aguzzi, Gabor G. Kovacs, Herbert Budka

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Excretion of Transmissible Spongiform Encephalopathy Infectivity in Urine by Luisa Gregori, Gabor G. Kovacs, Irina Alexeeva, Herbert Budka, Robert G. Rohwer

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Prion replication environment defines the fate of prion strain adaptation. by Elizaveta Katorcha, Nuria Gonzalez-Montalban, Natallia Makarava, Gabor G Kovacs, Ilia V Baskakov

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Disease-Specific α-Synuclein Seeding in Lewy Body Disease and Multiple System Atrophy Are Preserved in Formaldehyde-Fixed Paraffin-Embedded Human Brain by Ain Kim, Ivan Martinez-Valbuena, Jun Li, Anthony E. Lang, Gabor G. Kovacs

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Prediction of Autopsy Verified Neuropathological Change of Alzheimer’s Disease Using Machine Learning and MRI by Alexander Kautzky, Rene Seiger, Andreas Hahn, Peter Fischer, Wolfgang Krampla, Siegfried Kasper, Gabor G. Kovacs, Rupert Lanzenberger

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Cross-seeding of prions by aggregated α-synuclein leads to transmissible spongiform encephalopathy. by Elizaveta Katorcha, Natallia Makarava, Young Jin Lee, Iris Lindberg, Mervyn J Monteiro, Gabor G Kovacs, Ilia V Baskakov

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Fatal prion disease in a mouse model of genetic E200K Creutzfeldt-Jakob disease. by Yael Friedman-Levi, Zeev Meiner, Tamar Canello, Kati Frid, Gabor G Kovacs, Herbert Budka, Dana Avrahami, Ruth Gabizon

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Correction: Fatal Prion Disease in a Mouse Model of Genetic E200K Creutzfeldt-Jakob Disease. by Yael Friedman-Levi, Zeev Meiner, Tamar Canello, Kati Frid, Gabor G Kovacs, Herbert Budka, Dana Avrahami, Ruth Gabizon

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Pathologic correlates of aging-related tau astrogliopathy: ARTAG is associated with LATE-NC and cerebrovascular pathologies, but not with ADNC by Yuriko Katsumata, Xian Wu, Khine Zin Aung, Kathryn Gauthreaux, Charles Mock, Shelley L. Forrest, Gabor G. Kovacs, Peter T. Nelson

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SNCA and TPPP transcripts increase in oligodendroglial cytoplasmic inclusions in multiple system atrophy by Tomoya Kon, Shelley L. Forrest, Seojin Lee, Jun Li, Helen Chasiotis, Nasna Nassir, Mohammed J. Uddin, Anthony E. Lang, Gabor G. Kovacs

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Histotype-Dependent Oligodendroglial PrP Pathology in Sporadic CJD: A Frequent Feature of the M2C “Strain” by Ellen Gelpi, Sigrid Klotz, Nuria Vidal-Robau, Gerda Ricken, Günther Regelsberger, Thomas Ströbel, Ognian Kalev, Marlene Leoni, Herbert Budka, Gabor G. Kovacs

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Neuronal SNCA transcription during Lewy body formation by Tomoya Kon, Shelley L. Forrest, Seojin Lee, Ivan Martinez‑Valbuena, Jun Li, Nasna Nassir, Mohammed J. Uddin, Anthony E. Lang, Gabor G. Kovacs

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CpG and non-CpG Presenilin1 methylation pattern in course of neurodevelopment and neurodegeneration is associated with gene expression in human and murine brain by Noemi Monti, Rosaria A. Cavallaro, Andrea Stoccoro, Vincenzina Nicolia, Sigfrido Scarpa, Gabor G. Kovacs, Maria Teresa Fiorenza, Marco Lucarelli, Eleonora Aronica, Isidre Ferrer, Fabio Coppedè, Aron M. Troen, Andrea Fuso

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The G51D SNCA mutation generates a slowly progressive α-synuclein strain in early-onset Parkinson’s disease by Heather H. C. Lau, Ivan Martinez-Valbuena, Raphaella W. L. So, Surabhi Mehra, Nicholas R. G. Silver, Alison Mao, Erica Stuart, Cian Schmitt-Ulms, Bradley T. Hyman, Martin Ingelsson, Gabor G. Kovacs, Joel C. Watts

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Diagnostic Accuracy of Prion Disease Biomarkers in Iatrogenic Creutzfeldt-Jakob Disease by Franc Llorens, Anna Villar-Piqué, Peter Hermann, Matthias Schmitz, Olga Calero, Christiane Stehmann, Shannon Sarros, Fabio Moda, Isidre Ferrer, Anna Poleggi, Maurizio Pocchiari, Marcella Catania, Sigrid Klotz, Carl O’Regan, Francesca Brett, Josephine Heffernan, Anna Ladogana, Steven J. Collins, Miguel Calero, Gabor G. Kovacs, Inga Zerr

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Sporadic Creutzfeldt-Jakob disease VM1: phenotypic and molecular characterization of a novel subtype of human prion disease by Ellen Gelpi, Simone Baiardi, Carlos Nos, Sofia Dellavalle, Iban Aldecoa, Raquel Ruiz-Garcia, Lourdes Ispierto, Domingo Escudero, Virgina Casado, Elena Barranco, Anuncia Boltes, Laura Molina-Porcel, Nuria Bargalló, Marcello Rossi, Angela Mammana, Dorina Tiple, Luana Vaianella, Elisabeth Stoegmann, Ingrid Simonitsch-Klupp, Gregor Kasprian, Sigrid Klotz, Romana Höftberger, Herbert Budka, Gabor G. Kovacs, Isidre Ferrer, Sabina Capellari, Raquel Sanchez-Valle, Piero Parchi

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